Advertisement
JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

Originally published In Press as doi:10.1074/jbc.M302037200 on July 9, 2003

J. Biol. Chem., Vol. 278, Issue 42, 41409-41419, October 17, 2003
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
278/42/41409    most recent
M302037200v1
Right arrow Submit a Letter to Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Steinert, P. M.
Right arrow Articles by Marekov, L. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Steinert, P. M.
Right arrow Articles by Marekov, L. N.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Trichohyalin Mechanically Strengthens the Hair Follicle

MULTIPLE CROSS-BRIDGING ROLES IN THE INNER ROOT SHEATH*

Peter M. Steinert {dagger} {ddagger}, David A. D. Parry § and Lyuben N. Marekov {ddagger} 

From the {ddagger}Laboratory of Skin Biology, NIAMS, National Institutes of Health, Bethesda, Maryland 20892-8023 and the §Institute of Fundamental Sciences, Massey University, Palmerston North, Private Bag 11-222, New Zealand

Received for publication, February 26, 2003 , and in revised form, June 20, 2003.


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS AND DISCUSSION
 REFERENCES
 
Trichohyalin is expressed in specialized epithelia that are unusually mechanically strong, such as the inner root sheath cells of the hair follicle. We have previously shown that trichohyalin is sequentially subjected to post-synthetic modifications by peptidylarginine deaminases, which convert many of its arginines to citrullines, and by transglutaminases, which introduce intra- and interprotein chain cross-links. Here we have characterized in detail the proteins to which it becomes cross-linked in vivo in the inner root sheath of the mouse hair follicle. We suggest that it has three principal roles. First, it serves as an interfilamentous matrix protein by becoming cross-linked both to itself and to the head and tail end domains of the inner root sheath keratin intermediate filament chains. A new antibody reveals that arginines of the tail domains of the keratins are modified to citrullines before cross-linking, which clarifies previous studies. Second, trichohyalin serves as a cross-bridging reinforcement protein of the cornified cell envelope of the inner root sheath cells by becoming cross-linked to several known or novel barrier proteins, including involucrin, small proline-rich proteins, repetin, and epiplakin. Third, it coordinates linkage between the keratin filaments and cell envelope to form a seamless continuum. Together, our new data document that trichohyalin is a multi-functional cross-bridging protein that functions in the inner root sheath and perhaps in other specialized epithelial tissues by conferring to and coordinating mechanical strength between their peripheral cell envelope barrier structures and their cytoplasmic keratin filament networks.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
EXPERIMENTAL PROCEDURES
 RESULTS AND DISCUSSION
 REFERENCES
 
Native trichohyalin (THH)1 is a large highly charged {alpha}-helix-rich and insoluble protein that is expressed in specialized mammalian epithelial cell types (1–3). The tissues in which it is most abundantly expressed include the inner root sheath (IRS) cells of the hair follicle (approximately one third of total protein) (4, 5) and the medulla, a central column of cells within many coarse hairs (most of total protein) (4–6). THH is also expressed in trace amounts in other tissues such as newborn human foreskin epidermis, the hard palate, and rodent forestomach alone (6–11), or colocalized with filaggrin in hybrid granules in the filiform ridges of the tongue, the nail bed, and hyperplastic epidermis in skin diseases (11). Interestingly, each of these tissues is especially hardened or toughened to withstand mechanical abrasion and wear-and-tear during normal use. Thus, the question has arisen as to whether and how THH might contribute greater mechanical strength to these tissues (12).

THH can be recovered intact from these tissues only before their terminal differentiation (1, 5). However, recovery from mature tissues requires proteolysis (13–15) because it is subjected to extensive postsynthetic modification. First, many of its arginine residues are modified to citrullines (14–16) by a group of enzymes termed peptidylarginine deiminases (PAD) (17–23). In the case of THH in vitro, this reaction destroys its {alpha}-helical structure to a random coil, makes it more soluble in physiological buffers, and thereby apparently renders it more amenable to subsequent modifications (Fig. 1) (24). An important second modification is cross-linking by transglutaminase (TGase) enzymes (25, 26), which catalyze the formation of an isopeptide bond between peptide-bound glutamine and lysine residues; the net result is a stable insoluble protein polymer complex (27–31). In the case of the medulla cells, the amorphous THH protein is extensively cross-linked to itself. In the nearby IRS cells of the hair follicle, there is also a very high content of cross-link (26, 32). Earlier data suggested that these may link THH to the keratin intermediate filaments (KIF) characteristic of this tissue because KIF can be released from mature IRS cells only after a brief proteolytic digestion step (14) that clips off keratin head and/or tail domain sequences (32). In addition, we have identified a few cross-linked peptides involving THH linked to several barrier protein components of the cell envelope (CE) of mouse forestomach tissue (12).



View larger version (24K):
[in this window]
[in a new window]
  		FIG. 1.
Drawing representing the orderly posttranslational modifications of THH. From left to right, the rod-shaped, {alpha}-helical THH (red) accumulates as clusters along the KIF (blue). PAD initiates deimination of THH dispersing the more soluble citrulline form (yellow). Deimination proceeds together with initiation of cross-links (green). In the final stage multiple cross-links between THH and KIF align the filaments in a rigid structure. Figure is adapted from a previously published model (7).

 

The purpose of this study is to fully characterize the utilization of THH in the IRS tissue in which it is abundantly expressed. Our new protein sequence data provide robust support for the biomechanical role of THH in stabilization of cell structure by coordination of the CE with the KIF·THH complex within the IRS cells.


   EXPERIMENTAL PROCEDURES
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
RESULTS AND DISCUSSION
 REFERENCES
 
Preparation of Mouse IRS Tissue
IRS tissue was harvested from the hair follicles of newborn albino mice (32). Hair follicles isolated from trunk skin dermis of newborn (<1 day old) albino mice (33) were extracted in a buffer of 25 mM Tris-HCl (pH 8.0) containing 8 M urea. This buffer dissolves the lower portions of the hair follicles, thereby releasing the mature hardened IRS tissues as discrete conical, cylindrical multicellular structures. It does not appreciably dissolve the detached hair fiber material. The urea suspension was filtered through nylon gauze (pore size approximately 0.2 mm) through which the IRS tissues pass but hair fibers do not. In our experience, approximately 60% of the mass of these hair follicles is IRS tissue; the hair fiber cortical tissue is still poorly developed, and there are no hair fibers. The highly enriched IRS tissue was pelleted by centrifugation at 100 x g and gently washed in phosphate-buffered saline to remove urea but not to dissociate the IRS. We found in preliminary sequencing experiments that mouse IRS tissue was contaminated by solubilized outer root sheath proteins, particularly K6a and K16. To obtain a fraction enriched in KIF proteins (34), newborn mouse hair follicles were homogenized by sonication in phosphate-buffered saline containing 0.5 M KCl, and a protease mixture kit (Roche). This suspension was made to 5 mM MgCl2 and 100 mg/ml DNase I and incubated at <4 °C for 30 min, and then made to 0.1% Triton X-100 to dissolve membranes (34). Insoluble material, consisting almost entirely of KIF and THH granules, was then pelleted at 14,000 x g, dissolved in gel sample buffer, and resolved on 8–16% gradient polyacrylamide gels (Novex, Invitrogen).

Isolation of KIF and Three Peptide Fractions
The recovery of three protein fractions for subsequent sequencing analyses was performed as illustrated in Fig. 2.



View larger version (23K):
[in this window]
[in a new window]
  		FIG. 2.
Schema of derivation of fractions studied. The amounts of cross-link (purple) and ratios of arginines converted to citrullines (orange) are shown.

 

Fraction A Peptides—First, IRS KIF were harvested following limited trypsin digestion (32). Pellets of IRS were resuspended in 25 mM sodium phosphate (pH 8.0) (2 mg/ml) and digested with sequencing grade trypsin (Sigma) (0.5 mg/ml) for 10 min at 23 °C, and terminated by addition of a 1.5-fold molar excess of trypsin inhibitor (Sigma). This dissociated the IRS tissues into single cells that were pelleted at 500 x g and washed in phosphate buffer to remove enzymes. The cells were resuspended at the same concentration, chilled to 4 °C, and sonicated for 30 s (three 10-s bursts). Cellular debris was removed by centrifugation at 10,000 x g for 15 min. The KIF retained in the supernatant were pelleted at 100,000 x g in an Airfuge (Beckman Instruments). They were then dissociated in phosphate buffer containing 0.5% SDS and 1 mM dithiothreitol, and fractionated on a 95 x 2-cm column of Sephadex G-200 (32). Three protein peaks were recovered for further analyses. The broad low molecular weight fraction (Vt) was collected and further digested to completion with trypsin (1% by weight for 16 h at 37 °C), and peptides were retained for HPLC separation.

Fraction B Peptides—Alternatively, purified IRS tissue was digested to completion (1% by weight for 16 h at 37 °C) in a buffer of 0.1 M N-ethylmorpholine acetate (pH 8.0) with endopeptidase Asp-N (sequencing grade) (Roche Molecular Biochemicals, Mannheim, Germany). This procedure was used to solubilize cytoplasmic THH and KIF proteins without significantly proteolyzing CEs, the proteins of which generally contain few aspartic acid residues. The solubilized material was recovered by centrifugation at 15,000 x g for 15 min, digested further with trypsin (1% by weight for 3 h), and retained for HPLC separation.

Fraction C Peptides—The Asp-N pellet described above consisted almost entirely of intact or fragments of CEs, presumably mostly from the cuticle IRS cells. These were further digested in the same buffer with proteinase K (Invitrogen, 3% by weight for 3 h), clarified by centrifugation at 15,000 x g for 15 min, and the solubilized material used for HPLC separation.

Protein Chemical and Sequencing Procedures
Amino acid analysis was routinely used to measure protein amounts. Amounts of citrulline were corrected for hydrolytic losses to ornithine as described previously (24). The amount of isodipeptide cross-link was measured following total enzymic digestion of desired fractions and then quantitated by amino acid analysis (35). Negative controls included peptides known not to contain the cross-link or samples of an unmodified expressed portion of human THH termed THH-8 (7, 24). Peptides suspected of containing cross-links recovered from the three fractions described above were resolved by HPLC on a 2.1 x 250-mm C18 column (Phenomenex, Torrance, CA) with a flow rate of 0.25 ml/min and an acetonitrile gradient of 5–60% (90 min) followed by 60–95% (15 min). We harvested those peptides eluted with >30% acetonitrile, covalently attached them to a solid support, and performed sequencing for up to 15 Edman degradation cycles as described previously (7, 12). Empirically we found that such peptide species contained >15 residues and collectively accounted for >90% of the total cross-link content of the samples. Additionally, on sequencing, these typically contained two or more peptide "branches" adjoined by one or more cross-links. Sequences could be assigned from data base searches. The phenylthiohydantoin derivative of citrulline eluted at the same time as threonine in our system (Porton LF-3000 gas phase), and assignment was rarely in doubt because of the paucity of threonine in the proteins.

Generation of Polyclonal Antibodies and Indirect Immunofluorescence Procedures
Peptides corresponding the carboxyl terminus of mouse c29 protein (36) of sequence STKVNKTEQRIPS (IRSwt) and STKVNKTEQZIPS (IRScit) were synthesized, coupled to an 8-branched inert matrix, and used to generate polyclonal antibodies in guinea pigs, which were subsequently affinity-purified using the peptide antigen. Frozen serial sections of 5-day-old mouse skin (7 mm) were used for indirect immunofluorescence methods exactly as described previously (7). Primary antibodies used were: polyclonal rabbit anti-THH-8 (dilution 1:30) (7), polyclonal goat anti-human TGase 1 (dilution 1:50) (37), polyclonal guinea pig anti-IRSwt (dilution 1:100), polyclonal guinea pig anti-IRScit (dilution 1:200), and mouse monoclonal anti-K6 (Roche Molecular Biochemicals). Primary antibodies were then visualized using the appropriate affinity-purified secondary antibodies (Cappel Organon Technika Corp., Durham, NC) (7). Western blotting, dot blotting, and immunoprecipitation methods were used exactly as described usbpreviously (7).


   RESULTS AND DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS AND DISCUSSION
REFERENCES
 
The purpose of this study is to more fully characterize the utilization and function of THH in a tissue in which it is abundantly expressed: the IRS of the mouse hair follicle. We generated three different fractions of peptides (Fig. 2) designed to separately explore the possible multiple functions of THH. The amounts of cross-link and citrulline were measured. Numerous peptides containing cross-links from each fraction were sequenced. Table I lists and sorts the protein partners. Each will be discussed in detail below.


View this table:
[in this window]
[in a new window]
  		TABLE I
Summary of numbers of protein partners in sequenced peptides

 


View this table:
[in this window]
[in a new window]
  		TABLE III
KIF chains are cross-linked by way of their head and tail domains exclusively to domains 6 and 8 of mouse THH

Z, citrulline; single-letter code for amino acids is used. Residues in parentheses are predicted to precede or follow on the tryptic peptide sequence. Residues in lowercase letters were not identified by sequencing but are predicted from the known mouse THH sequence.

 

View this table:
[in this window]
[in a new window]
  		TABLE IV
Predominantly domains 2-5* of THH are used to cross-link to CE proteins

 
Comparison of THH Sequences—The sequences of human (1897 residues; Ref. 2), rabbit (1407 residues; accession no. P37709 [GenBank] ), mouse (1439 residues, accession no. XP_177952), and sheep (1549 residues; Ref. 3) THH proteins are available. All display marked similarities, yet notable differences; they consist of varying numbers of predominantly {alpha}-helical, highly charged quasi-repeating peptide motifs that are poorly conserved although recognizably similar between species. Human THH has been divided into nine domains, based on regions of either high or low sequence regularity among adjacent repeats (2). By use of the University of Wisconsin Genomics Computer Group software, domain 1 of mouse THH consists of two well defined EF-hand repeats (residues 1–95), domain 2 (96–243), and domains 3 and 4 (244–373), each similar to human THH. Next, its domain 5 (residues 374–595) consists of irregular sequence repeats of lower overall predicted {alpha}-helical content, roughly corresponding to human domains 5 and 7. Residues 596–697 define a region here termed domain 5* of weakly defined repeats unique to mouse THH. Residues 698–880 and 881–1406 of mouse THH define sets of well ordered sequences of different repeat motifs that are equivalent to human domains 6 and 8, respectively. Finally, domain 9 (residues 1407–1439) is homologous to human.

Direct Evidence That THH Functions as an Interfilamentous KIF Cross-bridging Protein in the IRS—KIF were harvested from mature IRS by use of a preliminary limited trypsin digestion (14, 32), which generated a KIF yield of approximately 40% of total IRS protein mass. Some of the cellular debris after brief trypsinization consisted of clumps of KIF apparently still cross-linked together. Unlike all other types of IF we have investigated, these IRS KIF are rigid straight rods that have a central densely staining core (Fig. 3A). This is reminiscent of the core observed in the center of the distinctly different trichocyte KIF of the adjacent hair fiber cortical cells (38). The KIF were pelleted and dissolved in SDS buffer. Upon fractionation by column chromatography, three peaks were recovered (Fig. 3B). The first and second peaks contained only traces of cross-link (<1 residue/1000 residues) and citrulline (ratio < 0.01), and presumably contained somewhat pruned IF chains, as judged by their high {alpha}-helix contents (data not shown). However, the peak eluted at Vt contained >90% of the citrulline and isopeptide cross-link of the isolated KIF.



View larger version (87K):
[in this window]
[in a new window]
  		FIG. 3.
Recovery of mouse IRS KIF. A, electron microscopy. Samples were deposited on a grid precoated with poly-L-lysine and negatively stained with 0.7% uranyl acetate. Bar = 100 nm. B, fractionation of SDS-dissolved KIF. The Vt peak was used to obtain fraction A peptides.

 

This Vt material, termed fraction A, was further digested to completion with trypsin and the peptides resolved by HPLC (Fig. 4A). From the resultant reproducible profile, we recovered 38 well resolved peaks that reflect quantitatively major species. Sequencing revealed that 35 possessed one or more cross-links; 28 peptides had one cross-link, 4 had two cross-links, and 3 had three cross-links, so that a total of 44 peptide partners was found (Tables I and III). Together, these are likely to be highly representative, as they accounted for 69% of the total cross-link and 73% of the total citrulline content of the Vt fraction. It remains likely, however, that many other minor peptide/protein species have been overlooked. Another 20 peptides involving KIF chains, having a total of 30 partners, were recovered from fraction B (Fig. 4C and Table III).



View larger version (35K):
[in this window]
[in a new window]
  		FIG. 4.
HPLC fractionation of peptides generated from fractions studied. A, fraction A; B, fraction C; C, fraction B.

 

Analyses of the combined data revealed two types of sequences: those from THH, and those from type I and type II keratin chains. For THH, all cross-links involved sequences of the highly regular domain 6 and 8 regions and the consensus THH peptide sequences involved were DZK(F/I)(Z/R)(Z/R) for the lysine residues and (E/Z)EQE(Z/L)Z for the glutamine residues. Based on ongoing studies of murine, ovine, and human data, the IRS uniquely expresses a set of least three (ovine) type I keratin chains (39–42). One mouse sequence (KRT1-c29) has been reported (39), which has highest homology to the sheep type I IRSa3 proteins (36). Our new sequencing data reveal that tail domain sequences of c29 were commonly found to participate in cross-linking, and that its arginines were usually modified to citrullines (Tables II and III). Further, three other homologous sequences were found (Table II) that may represent polymorphisms of this protein, or other mouse type I IRS keratins that perhaps correspond to the additional known sheep proteins for which only limited data have been reported. Several other sequences matched a known type II keratin chain expressed in IRS tissue (41, 42), but we cannot exclude the possibility that other K6-like type II IRS chains might be present in minor amounts, or might possess identical sequences around cross-linking sites. All of the keratin sequences were from end domains, with most from the tail. This may be because there are few Gln and Lys residues in the head domain sequences and because the tails may be more readily accessible for cross-linking. No links were obtained from central rod domain/linker Gln and Lys residues, but we cannot exclude that such linkages occur in minor amounts. This may be because the rod domain Gln and Lys residues are relatively inaccessible because of intra- and/or interchain molecular interactions.


View this table:
[in this window]
[in a new window]
  		TABLE II
Identities and similarities of mouse IRS type I keratin tail sequences recovered in this work

Mouse c29 type I keratin sequence is from Ref 39. Other data were found in this work. Single-letter code is used. Many arginines (R) were identified as citrullines (Z, orange). Lysines (K, red) and glutamines (Q, green) participated in cross-links. Note that gaps denote regions not recovered in sequenced peptides.

 

The data suggest that cross-linking of the IRS KIF is managed differently from the epidermis and in other epithelia studied heretofore. In the case of normal epidermis for example, essentially only the "KSISIS" Lys residue in the head domain of the type II keratin chains is used for KIF cross-linking and at only approximately 10% efficiency (43); only trace amounts of cross-links were found with other head or tail domain Lys and Gln residues (43). However, the KSISIS motif is not present on the IRS K6 protein (42). In case of the IRS KIF in the present study, multiple Lys and Gln residues were used in both the type I and type II chains (Tables II and III). Moreover, there is total of approximately 1.4 mol of cross-link/mol of KIF chains within the IRS tissue. This number is derived in three ways. First, the total KIF material released from IRS by brief trypsinization is 1 residue of cross-link/310 residues (Fig. 2), which translates to 1.4 mol of cross-link/mol of intact KIF chains. Second, the Vt material (15% of total KIF mass) contained 1 residue of cross-link/50 residues (Fig. 2), or 1.3 cross-links/intact KIF chain. Third, yields of peptides containing a cross-link described in Table III (fraction A peptides) total approximately 1.3 mol of cross-link/mol for all c29 keratins and 1.8 mol/mol for the K6IRS keratin. Together, these yields are far higher than the level of ~0.01 mol of cross-link/mol of keratin chains of the epidermis. This number is derived as follows; in normal epidermis the only keratin chains known to be cross-linked are those associated with the CE, which is 10% of cell protein, of which the keratin content is typically 1–5% (43).

The requirement for more cross-linking may explain why the IRS K6-like type II protein has devolved the specific KSISIS motif. We think the far higher degree of cross-linking of IRS KIF reflects the special rigidity requirements of the IRS in comparison to the flexibility required in the epidermis. Moreover, the recovery of peptides 28, 30–35, and 48–55 strongly suggests that THH serves as a cross-bridging protein among the KIF by indirectly linking head-to-head (peptide 35), head-to-tail (peptides 33, 48, 50, and 55), and tail-to-tail (several) sequences to form a continuous rigid composite structure.

Temporal Order of Modification of Mouse IRS KIF—We note that, in both head and tail keratin sequences, arginines were commonly modified to citrullines, and that each Gln and Lys residue was variably used for cross-linking. Thus, a question arises as to the temporal order of these two modification events. Previously, based on in vitro assays with THH-8, representing the terminal 40% of human THH, we suggested that its arginine residues should be modified first, to render it more soluble and accessible for subsequent cross-linking (7). However, it is unknown how and when the KIF end domains are modified, as multiple PAD enzymes and TGases co-exist with the KIF in the IRS cells (7, 22, 45–48).

To further explore this question, we raised in guinea pigs two polyclonal antibodies to the wild-type and citrulline form of the terminal 13 residues of the mouse c29 type I IRS KIF protein, and used them for studies on mouse hair follicle proteins. Both antibodies cross-reacted with the same select bands of monomeric KIF bands extracted from whole mouse hair follicle tissue (Fig. 5). Thus, some of the c29 protein had been modified by PAD enzymes. To confirm this, we performed immunoprecipitation reactions, and then measured citrulline contents of the precipitates. Only the products of the IRScit antibody contained citrulline. In addition, the IRScit antibody also recognized higher molecular weight bands (Fig. 5, lane 3).



View larger version (59K):
[in this window]
[in a new window]
  		FIG. 5.
Western blots reveal that the IRSwt and IRScit antibodies cross-react with KIF chains. Lane 1, Coomassie staining of total extracted mouse hair follicle proteins. Arrows mark likely intact mouse THH (upper) and actin (lower) proteins. Lane 2, same but transferred to Nytran and detected with IRSwt antibody. Lane 3, detected with IRScit antibody.

 

By use of indirect immunofluorescence, we found that the wild-type antibody stained the entire IRS (Fig. 6, B and C), beginning near the base of the follicle with the Henle cell layer, but within a few cell lengths, the Huxley and then cuticle cell columns as well. However, the IRScit antibody decoration started many cell lengths from the bottom of IRS KIF expression; stained the Henle, Huxley, and cuticle layers simultaneously; and then ceased a few cell lengths later (Figs. 6 (E and F), 7 (D and F), and 8 (A, C, D, and F)). Neither antibody stained the medulla (Figs. 6, 7, 8) or the companion layer (note gap between K6a in Fig. 7F), as predicted based on the expected absence of these type I IRS keratins. Thus, some but not all of the type I c29 protein is modified by the PAD enzymes. To confirm this, by use of dot-blotting methods, the IRScit antibody readily cross-reacted with its IRScit peptide antigen, that is, in which the Arg had been substituted and in which the Lys and Gln residues had not been modified by cross-linking. However, it cross-reacted only weakly with the IRSwt peptide, consistent with the immunofluorescence data. This result also specifies that the IRScit antibody reacts with a subset of the protein of Fig. 5. However, the protein in which the arginines are modified becomes no longer detectable within a few cell lengths along the IRS. To confirm that this loss of epitope was the result of TGase cross-linking, we performed two additional experiments. First, the IRScit antibody did not react on blots with peptides 30, 32, 33, or 55 from Table III in which the arginine residue had been modified to citrullines and nearby Lys and/or Gln residues participated in cross-links. As a control the antibody still recognized the peptide STKVNKTEQZIPS. Second, we explored TGase expression. In confirmation of earlier data (7), the TGase 3 enzyme is expressed only in that part of the IRS above the reactive zone of the IRScit antibody (Fig. 8C). However, the TGase 1 enzyme is present throughout the IRS (Fig. 8E) and co-localizes with the zone of IRScit antibody reactivity (Fig. 8F). These data suggest that cross-linking by the TGase 3 enzyme may account for the loss of the epitopes for the IRScit antibody.



View larger version (71K):
[in this window]
[in a new window]
  		FIG. 6.
Localization of THH, IRSwt, and IRScit antigens on serial sections of hair follicles of newborn mouse skin. Antibodies used were as follows: A and D, THH-8; B, IRSwt; C, both; E, IRScit; F, both THH-8 and IRScit. Bar = 50 µm.

 


View larger version (92K):
[in this window]
[in a new window]
  		FIG. 7.
Localization of THH, IRScit, and K6a antigens. Antibodies used were as follows: A, THH-8; B, K6; C, both; D, IRScit; E, K6; F, both. Bar = 50 µm.

 


View larger version (97K):
[in this window]
[in a new window]
  		FIG. 8.
Localization of THH, IRScit, TGase 1, and TGase 3 antigens. Antibodies used were as follows: A, IRScit; B, TGase 3; C, both; D, IRScit; E, TGase 1; F, both. Bar = 50 µm.

 

Direct Evidence That THH Functions as a Major Reinforcement Protein of IRS CEs—Mouse IRS tissue was digested to completion with Asp-N peptidase to generate soluble fraction B peptides consisting of the bulk of the KIF/THH cytoplasmic constituents (Fig. 2) (see below). The insoluble residue (recovered by centrifugation at 15,000 x g for 15 min) consisted principally of translucent rigid cellular shells or fragments thereof that appear identical to CEs of cornified epidermal cells (data not shown). However, the precise cell type of origin of these structures is not clear. Based on ultrastructural morphological studies, the IRS cuticle cells do form a barrier structure but it is less clear whether the Henle and Huxley cells do as well (4, 5). However, by earlier immunohistological criteria, all IRS cell layers appear to express involucrin and SPR proteins (49), suggesting that all IRS cell types may build a physical barrier entity. The total amino acid content revealed little citrulline and more modest contents of cross-link, comparable with that found in epidermal CEs (35, 43) (Fig. 2).

To generate the CE peptide fragment pool (fraction C), these were digested to completion with proteinase K. 85–95% of protein material was solubilized, and the peptides were resolved into many peaks by C18 reverse phase HPLC (Fig. 4B). In preliminary bulk analyses, the 35% of peptide mass eluted by <30% acetonitrile contained <10% of the total isopeptide cross-link. Accordingly, we collected 71 peaks resolved by >30% acetonitrile for sequencing. Of these, 63 generated identifiable sequence information, for which 48 contained one cross-link, 15 contained two cross-links, and 4 contained three cross-links, and altogether, presented 157 peptide partners (Tables IV and V). These accounted for 78% of the cross-link content of the fraction C CE fragment pool. Of the total, 34 involved links between THH and various known or novel CE proteins and 41 involved CE-CE links (Tables I, IV, and V). Listed also are an additional seven peptides (10 partner pairs) from fraction B.


View this table:
[in this window]
[in a new window]
  		TABLE V
Frequency of cross-links between protein partners in mouse IRS CEs

 

Several observations are apparent.

  1. The nature of the cross-linked peptides strongly implies that IRS CEs are built the same way as all other CEs we have studied (12, 50–52). They consist of a scaffold of "early" CE proteins such as involucrin, desmoplakin, envoplakin, and SPRs. This in turn is overlayered by specialized reinforcement proteins, which in this case is predominantly THH mixed with a variety of other proteins such as SPRs, repetin, LEP proteins, and epiplakin (below).
  2. THH was cross-linked to all other CE proteins, including predicted early CE "scaffold" proteins such as involucrin, envoplakin, and desmoplakin (Table V). The most frequently recovered cross-links were with involucrin, keratin, repetin, SPRs, and LEP. The THH peptides were derived from its entire sequence, except for the predicted EF-hand motifs at the amino terminus or domain 9 at the carboxyl terminus (and see Table VI). Many were from the less-ordered domains 5 and 5* of THH, but few were from the domains 6 or 8 to which KIF were exclusively cross-linked. Notably, peptides 46, 50, 57, 58, 69, and 70 demonstrate that THH serves as a cross-bridging protein between a variety of CE proteins. Moreover, peptides 52, 59, and 62 show that THH serves as a cross-bridging protein between the scaffold/reinforcement aspects of the CE and the KIF/THH cytoskeleton of the IRS cells.
  3. Small proline-rich (SPR) protein 1 and 2 families constituted the second principal set of IRS CE proteins, and one or the other was cross-linked to all other CE proteins. Because most members of the SPR2 family share the same amino and carboxyl termini involved in cross-linking (53), we cannot ascertain which specific SPR2 members are expressed in the IRS tissue. However, as found before, none of its central repeating peptide repeats was utilized for cross-linking.
  4. LEP proteins (54, 55) could be unambiguously assigned on 10 occasions, because of characteristic Cys residues, and this report is the first direct documentation of their role in a CE structure. However, as the short peptide fragments recovered after proteolysis are either identical or almost identical to those of SPR1 proteins, it is possible some were misassigned, as was likely in previous studies (12, 50). Nevertheless, based on their cross-linking partners (Tables IV and V), THH, LEP (see, for example, peptides 48, 50, 53 and 61), and SPR (many peptides) all appear to function as cross-bridging proteins, either among themselves and/or between the several other CE proteins. As LEP and SPR proteins are abundantly expressed in IRS tissue (50–53), we thus predict that they together with THH serve coincident and perhaps complementary roles as reinforcement proteins in IRS CEs.
  5. Repetin sequences were recovered in 11 cross-links, in an apparent cross-bridging role also (see peptides 51, 56, 60, and 63 of Table IV), and so this study confirms for the first time the involvement of this protein in a CE barrier structure (56). The new data document that repetin likely serves as a complete substrate; multiple adjacent different glutamines and lysines were used for cross-linking in vivo. Repetin, like involucrin, also consists of a tandem array of peptide repeats that are unique to it, but are more conserved than those of THH. However, unlike those of SPRs but more similar to those of involucrin, repetin repeats were extensively used for cross-linking. Thus, even though repetin, THH, and SPRs all seem to function as cross-bridging proteins, there are important differences in the way in which they may function as cross-bridgers.
  6. Desmoplakin and envoplakin cross-links were abundant. Only two Lys and one Gln residue in desmoplakin and one Gln residue in envoplakin were used, as seen previously. These residues are located late in the "C plakin" domain region and are thereby suggestive of the high degree of specificity with which these proteins are used in the early stages of CE assembly (50).
  7. Epiplakin, a new member of the "plakin" family of cytolinkers (57), was found in seven cross-links (Table V). These will be discussed in more detail below.
  8. Finally, cross-links involving other known CE proteins including members of the S100 family of calcium-binding proteins, elafin, etc., were not found; this could be because they are not abundant components of IRS CEs.


View this table:
[in this window]
[in a new window]
  		TABLE VI
Sequences involved in cross-links demonstrate domain-specific preferences of partners

The numbers in parentheses reflect the ratio of numbers of occurrences found versus numbers expected for even distribution based on the domain's portion of THH. Thus, a ratio of 1.0 would suggest even distribution.

 

THH Is Extensively Cross-linked to Itself in IRS Tissue— Fraction B peptides were not well resolved by several HPLC methods used because of the presence of a very large number of different species (Fig. 4). Because there is no evidence for polymorphism of mouse THH, the most likely explanation is that the PAD and TGase modifications of THH are complex, leading to a bewildering number of possible peptides following cleavage. Nevertheless, we were able to recover 77 peptides that contained one (62 peptides), two (11 peptides), or three (4 peptides) cross-links that contained only THH sequences linked together (Table I) (sequence data not shown). These generated 173 THH peptide "arms." Six other THH arms were obtained from fraction C (Table I). Altogether in one experiment, these represented approximately 40% of the total cross-link and citrulline content of Asp-N-soluble IRS peptides. The large unresolved region late in the chromatogram contained an additional 53% of cross-link (one per 19 residues) and 48% of citrulline (ratio of 0.8).

Table VI summarizes the domain origins of all THH sequences recovered in this work. The data reveal domain-specific partner linkages, which suggests modification preferences. First, no links were found with the domain 1 EF-hand portion of THH. It is possible these motifs are removed during terminal differentiation, as occurs for the related protein, profilaggrin (58). All THH-keratin links involved only domain 6 or 8 sequences. THH-THH and THH-CE protein links were distributed among domains 2–5, but were rare in domains 6 and 8. Most intra-THH cross-links occurred in the least organized domain 5 region at a 3.5-fold higher frequency (Table VI).

A Possible Explanation as to Why KIF Cross-link Preferentially Only to Domains 6 and 8 —As for human THH, domains 6 and 8 represent the most orderly almost perfectly {alpha}-helical portion of mouse THH. In addition to regular sequence repeats, both domains exhibit a regular quasi-repeat of 20 residues in the distribution of their charged residues, which is equivalent to an axial rise of ~2.97 nm. The coiled-coil {alpha}-helical 1B and 2 rod domain segments of the c29 and K6IRS KIF chains, like all types I/II KIF chains (44), display a 9.8-residue repeat of charged residues, which corresponds to 1.46 nm of axial rise along the KIF. It is therefore likely the rod domains of the KIF and domains 6 and 8 of THH will engage in favorable ionic interactions, as the two periodicities will frequently "beat" together. This will not occur in a regular way with any other domain of THH. These favorable interactions will impact modification events by the PAD and TGase enzymes. First, as the tail (and possibly beginning of the head) domains of the KIF chains project laterally out from the wall of the KIF (44), they will be more accessible for modification events. Second, because of their close proximity, we predict the KIF end domains will be preferentially cross-linked to domains 6 and 8 to THH than any to other domain of THH. Third, cross-linking of THH to KIF rod domains is unlikely to occur because they are tightly packed together. Fourth, we predict that prior cross-linking of the KIF end domains to THH domains 6 and 8 will preclude their subsequent utilization for cross-linking to THH itself or other CE proteins.

Cross-links Involving the Novel "Plakin" Epiplakin—Five cross-links involving epiplakin in the fraction C peptides and two more in fraction B were recovered (Table IV). Human epiplakin consists largely of 13 highly conserved B or B-like plakin domains interspersed by linker regions (57). Our new sequence data reveal that the human and mouse species have been highly conserved at least around cross-linking sites. Three neighboring Gln residues were found that are repeated in its several B domains. All epiplakin links involve lysine residues from either THH or a keratin chain or both. As expected these peptides were derived from the intracellular milieu of the IRS tissue. Notably, peptide 71 suggests that epiplakin can act as a cross-bridger between the KIF proteins. Together, the data suggest that the role of epiplakin role in CE barrier formation and/or the cytoskeleton is different than for desmoplakin and envoplakin.

Summary—Our new data support the following timeline of events in the IRS. First, THH and KIF are coincidentally expressed from the lowermost cell layers of the IRS in the hair follicle (Fig. 6, A–C; Refs. 1, 4, and 5). Second, TGase 1 is expressed in all layers of the IRS starting also from the lowermost cell layers coincident with THH and KIF expression (Fig. 8, E and F), but the TGase 3 enzyme is expressed many cell layers higher in the follicle (Fig. 8, B and C). Third, compilation of existing data suggests that the PAD enzymes (45) are expressed well before the TGase 3 enzyme (Fig. 8, B and C). Fourth, it is therefore likely that modification of the arginines of the KIF chain end domains to citrullines occurs before a significant degree of cross-linking (Fig. 5). The reason why only some of the KIF chains are modified may be the result of accessibility limits imposed once some cross-linking has occurred. Fifth, very shortly later, only the domains 6 and 8 of THH are used for cross-linking to KIF end domains (Tables II and VI), possibly because of coincident regular distributions of ionic charges efficiently juxtapose the two proteins. Sixth, this specific cross-linking coincides with the expression of the TGase 3 enzyme (Fig. 8, B and C), which suggests TGase 3, rather than TGase 1, is responsible for THH-KIF cross-linking. Indeed, the TGase 3 enzyme exhibits marked preference for KIF and THH as substrates (43). Seventh, we note that the highest content of citrullines and cross-links occurred in the unresolved portion of fraction B (Fig. 4), and cross-bridging cross-linking of THH with CE proteins and itself used predominantly the less regular domains 2–5* (Tables IV, V, VI). Together, we propose that this further extensive cross-linking of THH occurs during later stages of IRS maturation. This domain specificity may occur because of steric restrictions imposed by earlier THH-KIF cross-linking, and because at later times these THH sequences may be more accessible to the TGases after complete denaturation of THH by PAD deimination. Thus, in summary, we envisage the following sequence of events for THH: (a) some PAD modification of KIF end domains and THH occurring early, (b) cross-linking of KIF end domains to THH domains 6 and 8, (c) further extensive PAD modification of THH, and (d) further extensive cross-linking of THH to itself and CE proteins. Finally, we cannot exclude the possible role of other TGase isoforms, in particular TGases 5, 6, and 7, in cross-linking in IRS cells.

Moreover, our data document that THH serves three concurrent and essential roles on the IRS. It serves as a KIF interfilamentous cross-linking protein by forming frequent links between the heads and tails of the keratin chains; it serves as a major reinforcement cross-bridging protein for the CE barrier structure of the IRS, in concert with the SPR, LEP, repetin, and epiplakin proteins; and, finally, THH serves to coordinate CE structure with that of the major KIF-THH cytoplasmic content into a continuous hardened protein assembly. Of all characterized TGase cross-linked products studied to date, the amount of cross-link in the IRS, roughly 1 residue in 30, is second only to that which occurs in the nearby medulla within the hair fiber shaft. This high degree of cross-linking mirrors to a certain extent events in the keratinized hair cortical cells, where 1 residue in 20 is a disulfide bond (59). This high degree of cross-linking forms a hardened rigid structure typical of hairs, nails, etc. Thus, by analogy, a similar degree of cross-linking with the above-mentioned partners in the IRS lends robust support to the concept that THH serves an important biomechanical role to provide a tough rigid texture to the IRS tissue. This in turn is essential for appropriate morphogenesis of hair follicle cortical cells internal to the IRS within the hair follicle (4, 5). Evolution may have chosen cross-linking by way of the isopeptide bonds in the IRS as a more favorable reaction in living cells than disulfide bond formation. Further, proteins made insoluble by isopeptide cross-linking are more easily degraded than are disulfide-bonded proteins, as indeed is required for the IRS, which is degraded within the follicle canal (4, 5). As suggested by Tobin et al. (60), "it is likely that [a lysosomal cysteine protease, cathepsin L] CTSL may... use trichohyalin as a protein substrate." Finally, we submit that THH serves a similar biomechanical role in other toughened epithelial tissues such as the hard palate, filiform ridges of the tongue, and rodent forestomach.


   FOOTNOTES
 
* The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. Back

{dagger} Shortly after this paper was submitted, Peter Steinert passed away unexpectedly as the result of an accident. D. A. D. P. and L. N. M. dedicate this work on trichohyalin to his memory. Back

To whom all correspondence should be addressed: Bldg. 50, Rm. 1531, NIAMS, National Institutes of Health, Bethesda, MD 208928023. Tel.: 301-496-7190; Fax: 301-402-3417; E-mail: marekovl{at}mail.nih.gov.

1 The abbreviations used are: THH, trichohyalin; CE, cell envelope; IRS, inner root sheath; KIF, keratin intermediate filaments; PAD, peptidylarginine deiminase; SPR, small proline-rich protein; TGase, transglutaminase; Z, single-letter code for citrulline; HPLC, high performance liquid chromatography. Back



   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 EXPERIMENTAL PROCEDURES
 RESULTS AND DISCUSSION
 REFERENCES
 

  1. Rothnagel, J. A. & Rogers, G. E. (1986) J. Cell Biol. 102, 1419–1429[Abstract/Free Full Text]
  2. Lee, S.-C., Kim, I.-G., Marekov, L. N., O'Keefe, E. J., Parry, D. A. D. & Steinert, P. M. (1993) J. Biol. Chem. 268, 12164–12176[Abstract/Free Full Text]
  3. Feitz, M. J., McLaughlin, C. J., Campbell, M. T. & Rogers, G. E. (1993) J. Cell Biol. 121, 855–865[Abstract/Free Full Text]
  4. Vörner, H. (1903) Dermatol. Z. (Berlin) 10, 357–376
  5. Auber, L. (1950) Trans. R. Soc. Edinb. 62, 191–254
  6. Hamilton, E. H., Payne, J., Richard, E. & O'Keefe, E. J. (1992) J. Invest. Dermatol. 96, 666–672[CrossRef]
  7. Tarcsa, E., Marekov, L. N., Andreoli, J., Idler, W. W., Candi, E., Chung, S.-I. & Steinert, P. M. (1997) J. Biol. Chem. 272, 27893–27901[Abstract/Free Full Text]
  8. O'Guin, M. W. & Manabe, M. (1991) Ann. N. Y. Acad. Sci. 642, 51–63[Medline] [Order article via Infotrieve]
  9. O'Guin, M. W., Sun, T.-T. & Manabe, M. (1992) J. Invest. Dermatol. 98, 24–32[CrossRef][Medline] [Order article via Infotrieve]
  10. O'Keefe, E. J., Hamilton, E., Lee, S.-C. & Steinert, P. M. (1993) J. Invest. Dermatol. 101, 65S-71S[CrossRef][Medline] [Order article via Infotrieve]
  11. Manabe, M. & O'Guin, M. W. (1994) Differentiation 58, 65–75[CrossRef][Medline] [Order article via Infotrieve]
  12. Steinert, P. M., Kartasova, T. & Marekov, L. N. (1998) J. Biol. Chem. 273, 11758–11769[Abstract/Free Full Text]
  13. Rogers, G. E. (1962) Nature 194, 1149[CrossRef][Medline] [Order article via Infotrieve]
  14. Steinert, P. M., Dyer, P. Y. & Rogers, G. E. (1969) J. Invest. Dermatol. 56, 49–54[CrossRef]
  15. Harding, H. W. J. & Rogers, G. E. (1976) Biochim. Biophys. Acta 427, 315–324[Medline] [Order article via Infotrieve]
  16. Rogers, G. E. (1963) J. Histochem. Cytochem. 11, 700–705[Abstract]
  17. Takahara, H., Oikawa, Y. & Suguwara, K. (1983) J. Biochem. (Tokyo) 94, 1945–1953[Abstract/Free Full Text]
  18. Rogers, G. E. & Rothnagel, J. A. (1983) in Normal and Abnormal Epidermal Differentiation (Seiji, M. & Bernstein, I. A., eds) pp. 171–184, University of Tokyo Press, Tokyo
  19. Watanabe, K., Aikyama, K., Hikichi, K., Ohtsuka, R., Okuyama, A. & Senshu, T. (1988) Biochim. Biophys. Acta 966, 375–383[Medline] [Order article via Infotrieve]
  20. Takahara, H., Tschida, M., Kusubata, M., Akutsu, K., Tagmi, S. & Suguwara, K. (1989) J. Biol. Chem. 264, 13361–13368[Abstract/Free Full Text]
  21. Terakawa, H., Takahara, H. & Suguwara, K. (1991) J. Biochem. (Tokyo) 110, 661–666[Abstract/Free Full Text]
  22. Kanno, T., Kawada, A., Yamanouchi, J., Yosida-Noro, C., Yoshiki, A., Shiraiwa, M., Kusakabe, M., Manabe, M., Tezuka, T. & Takahara, H. J. (2000). J. Invest. Dermatol. 115, 813–823[CrossRef][Medline] [Order article via Infotrieve]
  23. Shirai, H., Blundell, T. L. & Mizuguchi, K. (2001) Trends Biochem. Sci. 26, 465–468[CrossRef][Medline] [Order article via Infotrieve]
  24. Tarcsa, E., Marekov, L. N., Mei, G., Melino, G., Lee, S.-C. & Steinert, P. M. (1996) J. Biol. Chem. 271, 30709–30716[Abstract/Free Full Text]
  25. Harding, H. W. J. & Rogers, G. E. (1971) Biochemistry 10, 624–630[CrossRef][Medline] [Order article via Infotrieve]
  26. Harding, H. W. J. & Rogers, G. E. (1972) Biochemistry 11, 2858–2863[CrossRef][Medline] [Order article via Infotrieve]
  27. Lorand. L. & Conrad, S. M. (1984) Mol. Cell Biochem. 58, 9–35[CrossRef][Medline] [Order article via Infotrieve]
  28. Folk, J. E & Chung, S.-I. (1985) Methods Enzymol. 113, 358–375[Medline] [Order article via Infotrieve]
  29. Greenberg, C. S., Birckbichler, P. J. & Rice, R. H. (1991) FASEB J. 5, 3071–3077[Abstract]
  30. Nemes, Z. & Steinert, P. M. (1999) Exp. Mol. Med. 31, 5–19[Medline] [Order article via Infotrieve]
  31. Kim, S.-Y., Jeitner, T. M. & Steinert, P. M. (2002) Neurosci. Lett., 40, 85–103
  32. Steinert, P. M. (1978) Biochemistry 17, 5045–5052[CrossRef][Medline] [Order article via Infotrieve]
  33. Weinberg, W. C., Goodman, L. V., George, C., Morgan, D. L., Ledbetter, S., Yuspa, S. H. & Lichti, U. (1993) J. Invest. Dermatol. 100, 229–236[CrossRef][Medline] [Order article via Infotrieve]
  34. Steinert, P. M., Aynardi-Whitman, M., Zackroff, R. V. & Goldman, R. D. (1982) in Methods and Perspectives in Cell Biology; The Cytoskeleton, Part A: Cytoskeletal Proteins, Isolation and Characterization (Wilson, L., ed) Vol. 24, pp. 399–419, Academic Press Inc., New York
  35. Hohl, D., Mehrel, T., Lichti, U., Turner, M. L., Roop, D. R. & Steinert, P. M. (1991) J. Biol. Chem. 266, 6626–6636[Abstract/Free Full Text]
  36. Bawden, C. S., McLaughlin, C., Nesci, A. & Rogers, G. E. (2001) J. Invest. Dermatol. 116, 157–166[CrossRef][Medline] [Order article via Infotrieve]
  37. Kim, S.-Y., Chung, S.-I. & Steinert, P. M. (1995) J. Invest. Dermatol. 104, 211–217[CrossRef][Medline] [Order article via Infotrieve]
  38. Watts, N. R., Jones, L. N., Cheng, N., Wall, J. S., Parry, D. A. & Steven, A. C. (2002) J. Struct. Biol. 137, 109–119[CrossRef][Medline] [Order article via Infotrieve]
  39. Sato, H., Koide, T., Sagai, T., Ishiguro, S., Tamai, M., Saitou, N. & Shiroshi, T. (1999) Genomics 56, 303–309[CrossRef][Medline] [Order article via Infotrieve]
  40. Carninci, P., Shinata, Y., Hayatsu, N., Sugahara, Y., Shinata, K., Itoh, M., Konro, H., Okazaki, Y., Muramatsu, M. & Hayashizaki, Y. (2000) Genome Res. 10, 1617–1630[Abstract/Free Full Text]
  41. Hesse, M., Magin, T. M. & Weber, K. (2001) J. Cell Sci. 114, 2569–2575[Abstract/Free Full Text]
  42. Aoki, N., Sawada, S., Rogers, M. A., Schweizer, J., Shimomura, Y., Tsujimoto, T., Ito, K. & Ito, M. (2001) J. Invest. Dermatol. 116, 359–365[CrossRef][Medline] [Order article via Infotrieve]
  43. Candi, E., Tarcsa, E., DiGiovanna, J. J., Compton, J. G., Elias, P. M., Marekov, L. N. & Steinert, P. M. (1998) Proc. Natl. Acad. Sci. U. S. A. 95, 2067–2071[Abstract/Free Full Text]
  44. Parry, D. A. D. & Steinert, P. M. (1999) Quart. Rev. Biophys. 32, 99–187[CrossRef][Medline] [Order article via Infotrieve]
  45. Rogers, G. E., Winter, B., McLaughlin, C. S., Powell, B. & Nesci, T. (1997) J. Invest. Dermatol. 108, 700–707[CrossRef][Medline] [Order article via Infotrieve]
  46. Parenteau, N. L., Pilato, A. & Rice, R. H. (1986) Differentiation 33, 130–141[Medline] [Order article via Infotrieve]
  47. Tamada, Y., Takama, H., Kitamura, T., Ikeya, T. & Yockochi, T. (1995) Acta Dermato-Venerol. 75, 190–192[Medline] [Order article via Infotrieve]
  48. Polakowska, R. R., Piacentini, M., Bartlett, R., Goldsmith, L. A. & Haake, A. R. (1994) Dev. Dyn. 199, 176–188[Medline] [Order article via Infotrieve]
  49. Hohl, D., de Viragh, P. A., Amiguet-Barras, F., Gibbs, S., Backendorf, C. & Huber, M. J. (1995) J. Invest. Dermatol. 104, 902–909[CrossRef][Medline] [Order article via Infotrieve]
  50. Steinert, P. M. & Marekov, L. N. (1999) Mol. Biol. Cell 10, 4247–4261[Abstract/Free Full Text]
  51. Steinert, P. M. (2000) J. Cell Biol. 151, F5–F7[Abstract/Free Full Text]
  52. Kalinin, A., Kajava, A. & Steinert, P. M. (2002) BioEssays 24, 789–800[CrossRef][Medline] [Order article via Infotrieve]
  53. Song, H.-J., Poy, G., Darwiche, N., Lichti, U., Kuroki, T., Steinert, P. M. & Kartasova, (1999) Genomics 55, 28–42[CrossRef][Medline] [Order article via Infotrieve]
  54. Zhao, X.-P. & Elder, J. T. (1997) Genomics 45, 250–258[CrossRef][Medline] [Order article via Infotrieve]
  55. Marshall, D., Hardman, M. J., Neild, K. M. & Byrne, C. (2001) Proc. Natl. Acad. Sci. U. S. A. 98, 13031–13036[Abstract/Free Full Text]
  56. Krieg, P., Schuppler, M., Koesters, R., Mincheva, A., Lichter, P. & Marks, F. (1997) Genomics 43, 339–348[CrossRef][Medline] [Order article via Infotrieve]
  57. Fujiwara, S., Takeo, N., Otani, Y., Parry, D. A. D., Kunimatsu, M., Lu, R., Sasaki, M., Matsuo, N., Khaleduzzaman, M. & Yoshioka, H. (2001) J. Biol. Chem. 276, 13340–13347[Abstract/Free Full Text]
  58. Pearton, D. J., Dale, B. A. & Presland, R. B. (2002) J. Invest. Dermatol. 119, 661–669[CrossRef][Medline] [Order article via Infotrieve]
  59. Fraser, R. D. B., MacRae, T. P. & Rogers, G. E. (1972) Keratins: Their Composition, Structure and Biosynthesis, Charles C. Thomas, Springfield, IL
  60. Tobin, D. J., Foitzik, K., Reinheckel, T. Mecklenburg, L., Botchkarev, A. V., Peters, C. & Paus, R. (2002) Am. J. Pathol. 160, 1807–1821[Abstract/Free Full Text]

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
 J. Biol. Chem.Home page
K. Kizawa, H. Takahara, H. Troxler, P. Kleinert, U. Mochida, and C. W. Heizmann
Specific Citrullination Causes Assembly of a Globular S100A3 Homotetramer: A PUTATIVE Ca2+ MODULATOR MATURES HUMAN HAIR CUTICLE
J. Biol. Chem., February 22, 2008; 283(8): 5004 - 5013.
[Abstract] [Full Text] [PDF]

Home page
 Mol. Cell. Biol.Home page
M. Goto, H. Sumiyoshi, T. Sakai, R. Fassler, S. Ohashi, E. Adachi, H. Yoshioka, and S. Fujiwara
Elimination of Epiplakin by Gene Targeting Results in Acceleration of Keratinocyte Migration in Mice
Mol. Cell. Biol., January 15, 2006; 26(2): 548 - 558.
[Abstract] [Full Text] [PDF]

Home page
 Mol. Cell. Biol.Home page
D. Spazierer, P. Fuchs, S. Reipert, I. Fischer, M. Schmuth, H. Lassmann, and G. Wiche
Epiplakin Is Dispensable for Skin Barrier Function and for Integrity of Keratin Network Cytoarchitecture in Simple and Stratified Epithelia
Mol. Cell. Biol., January 15, 2006; 26(2): 559 - 568.
[Abstract] [Full Text] [PDF]

Home page
 J. Cell Sci.Home page
S.-I. Jang, A. Kalinin, K. Takahashi, L. N. Marekov, and P. M. Steinert
Characterization of human epiplakin: RNAi-mediated epiplakin depletion leads to the disruption of keratin and vimentin IF networks
J. Cell Sci., February 15, 2005; 118(4): 781 - 793.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
278/42/41409    most recent
M302037200v1
Right arrow Submit a Letter to Editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Steinert, P. M.
Right arrow Articles by Marekov, L. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Steinert, P. M.
Right arrow Articles by Marekov, L. N.
Social Bookmarking
Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 2003 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement