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J. Biol. Chem., Vol. 279, Issue 27, 28315-28319, July 2, 2004

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Interleukin-7 and Transforming Growth Factor- Play Counter-regulatory Roles in Protein Kinase C--dependent Control of Fibroblast Collagen Synthesis in Pulmonary Fibrosis^*

Ling Zhang, Michael P. Keane, Li X. Zhu, Sherven Sharma, Enrique Rozengurt, Robert M. Strieter, Steven M. Dubinett, and Min Huang¶||

From the ^¶Department of Pathology, Department of Medicine Division of Pulmonary and Critical Care Medicine, Department of Medicine Division of Digestive Diseases, David Geffen School of Medicine at UCLA and Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California 90095

Received for publication, March 16, 2004 , and in revised form, April 26, 2004.

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Transforming growth factor- (TGF-) is a potent fibrogenic factor responsible for promoting synthesis of extracellular matrix. Interleukin-7 (IL-7) inhibits TGF- signaling by up-regulating Smad7, a major inhibitor of the Smad family. In a variety of cells, TGF--mediated activation of target genes requires active protein kinase C- (PKC-) in addition to Smads (1). We determined the role of PKC- in the regulation of pulmonary fibroblast collagen synthesis in response to TGF- and IL-7 stimulation. Here we show that TGF- and IL-7 have opposing effects on PKC-; TGF- stimulates, while IL-7 inhibits, PKC- activity. IL-7 inhibits TGF--induced PKC- phosphorylation at Ser-645 and Thr-505. Inhibition of PKC- with specific small inhibitory RNA restores TGF--mediated induction of Smad7 and in parallel significantly reduces TGF--mediated collagen synthesis. Thus, PKC- may play a critical role in the pathogenesis of pulmonary fibrosis and may serve as a molecular target for therapeutic intervention to suppress fibrosis.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Pulmonary fibrosis is characterized by disturbances of extracellular matrix protein deposition resulting from fibroblast activation and proliferation (2). TGF-¹ is a major driving force in the pathogenesis of pulmonary fibrosis (2). Overexpression of TGF-1 in pulmonary fibrosis contributes to the dysregulation of normal homeostatic mechanisms at multiple levels; it enhances synthesis and deposition of extracellular matrix components including collagen and can also alter the balance of matrix metalloproteinases and their inhibitors (2, 3). TGF- signaling and regulation are mediated by a family of Smad proteins (4). TGF- induces phosphorylation of Smad2 and Smad3, which form hetero-oligomeric complex with Smad4 that translocate to the nucleus, where they recognize Smad binding elements to regulate transcriptional responses of target genes (4). Smad7 is a major inhibitory member of the Smad family (4). Smad7 inhibits TGF--mediated phosphorylation of Smad2/3 and competes with Smad2/3 for the binding to TGF- receptor. TGF- rapidly induces expression of Smad7 mRNA, suggesting a negative feedback loop to control TGF- signaling (4).

We have demonstrated that IL-7 possesses potent antifibrotic activities in vitro and in vivo (5). IL-7 inhibits TGF- signaling through the induction of Smad7 (5). In addition to Smads, TGF- requires active PKC- to activate its target genes in a variety of cells including pulmonary fibroblasts (1). PKC-, a ubiquitously expressed kinase involved in a variety of cellular signaling pathways, has been implicated in de novo synthesis of extracellular matrix components (6). PKC- participates in the up-regulation of type I (COL1A1) and type III (COL3A1) collagen gene expression mediated by TGF- in scleroderma fibroblasts (7). Based on the importance of PKC- in TGF- signaling, we determined whether PKC- modulated collagen synthesis in response to TGF- and IL-7 stimulation in pulmonary fibroblasts.

	MATERIALS AND METHODS

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Cell Culture—Isolation, passage, and specific cell marker characterization of human pulmonary fibroblasts were performed as described previously (5). Fibroblasts obtained from patients with idiopathic pulmonary fibrosis (PFF) or non-fibrotic lung diseases (NF) were maintained in 5% CO₂ in air as monolayers at 37 °C in 75-cm² tissue culture flasks containing 20 ml of Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum, 100 units/ml penicillin, 0.1 mg/ml streptomycin, and 2 mM glutamine (JRH Biosciences, Lenexa, KS).

Cytokines and Antibodies—Human recombinant TGF-1 (3.2 x 10⁴ units/µg) and recombinant human IL-7 (10⁵ units/µg) were obtained from R & D Systems, Minneapolis, MN. Rabbit anti-PKC-, rabbit anti-PKC--[Ser645], and rabbit anti-PKC--[pTyr311] antibodies were obtained from BIOSOURCE International, Inc., Camarillo, CA. Rabbit anti-PKC- [pThr505] antibody was obtained from Cell Signaling Technology, Inc., Beverly, MA. Lyophilized human recombinant TGF-1 was reconstructed in sterile 4 mM HCl containing 0.1% bovine serum albumin in a final concentration of 10 µg/ml and stored at –70 °C in aliquots.

Northern Blot Analysis—High quality total RNA from 10⁷ cells of NF and PFF was prepared by the TRIzol method (Invitrogen). Northern blotting was performed as previously described (8). We used the following unique 30-mer oligonucleotide probes for the detection of human COL1A1 and COL3A1 gene expression: 5'-CAGTTCTTGGTCTCGTCACAGATCACGTCA-3' (human COL1A1 probe, corresponding to the coding region 332–361) and 5'-TTCCATTTTCTCCTGGAGGACCACCTGTAC-3' (human COL3A1 probe, corresponding to the coding region 2051–2080). Duplicate filters were hybridized with ³²P-radiolabeled human -actin cDNA probe serving as controls for equal loading and transfer. The filters were exposed to an x-ray film for documentation and analyzed using phosphor imaging equipment (Molecular Imager, Bio-Rad).

PKC- Activity Assays—PFF and NF were incubated in medium alone, in medium containing IL-7 (100 ng/ml), in medium containing TGF-1 (10 ng/ml), or in medium containing IL-7 and TGF-1 for 1 h at 37 °C. 5 x 10⁶ Cells of each sample were lysed in phosphorylation lysis buffer containing 150 mM NaCl, 200 µM sodium orthovanadate, 10 mM sodium prophosphate, 100 mM sodium fluoride, 1.5 mM MgCl₂, 10% glycerol, 1 mM EDTA, 0.5% Triton X-100, and proteinase inhibitors. Cell lysates were immunoprecipitated with a specific anti-PKC- antibody (BIOSOURCE International, Inc.). The immunoprecipitates were washed three times with phosphorylation lysis buffer and two times with kinase buffer, which contains 25 mM Tris-HCl (pH 7.4), 5 mM MgCl₂, 0.5 mM EDTA, 1 mM dithiothreitol, 20 µg of phosphatidylserine, and 20 mM ATP. The immunoprecipitates were resuspended in 30 µl of kinase buffer containing 5 µg of an exogenous substrate histone H1 and 20 µCi of [-³²P]ATP and incubated at 25 °C for 30 min. The reaction was terminated by the addition of an equal volume of SDS sample buffer. The PKC- activity was determined by the amount of ³²P-histone H1 produced as detected by autoradiography following SDS-PAGE electrophoresis.

Western Blot Analysis—PFF and NF under standard growth conditions or in medium supplemented with cytokines were suspended in 1x phosphate-buffered saline buffer containing 1 mM MgCl₂, protease inhibitors (10 µl/ml), and 0.1% Triton X-100. The cell suspension was sonicated and then centrifuged at 11,000 x g for 10 min at 4 °C. Protein content of each sample was determined using the protein assay kit (Bio-Rad). Aliquots containing 80 µg of lysate were boiled for 5 min and electrophoresed on 7.5% polyacrylamide gels. The gels were transferred to Immuno-Blot membranes (Bio-Rad), blocked for 1 h with 5% nonfat milk, and then incubated with specific primary antibodies. The immunoreactive proteins were detected using a ProtoBlot II AP System kit (Promega Corp., Madison, WI).

PKC- siRNA—PKC- siRNA Duplex1 for the target sequence 5'-AAG ATG AAG GAG GCG CTC AG-3' was obtained from Qiagen (Valencia, CA). Two micrograms of PKC- siRNA were premixed with TransMessenger Transfection Reagent (Qiagen Inc., Valencia, CA) in a ratio of 1:2 to 1:8. PFF and NF were then transfected with PKC- siRNA mixture or solvent only as controls for 3 h under standard growth condition.

Real-time RT-PCR—Five hundred nanograms of total RNA from PFF (n = 2) and NF (n = 3) were used for the real-time RT-PCR analysis using unique target gene primers or housekeeping gene -actin primers serving as controls for equal loading. Primer pairs for the optimal real-time RT-PCR results were designed with the assistance of ongoing consultation with the technical team of the manufacturer (Bio-Rad). We used the following unique primer pairs for the detection of human Smad7 mRNA by the real-time RT-PCR: 5'-CTGCAACCCCCATCACCTTA-3' (Smad7 sense primer) and 5'-CCCTGTTTCAGCGGAGGAA-3' (Smad7 antisense primer). We used the following unique primer pairs for the detection of human -actin mRNA serving as controls for equal loading by the real-time RT-PCR: 5'-GATGAGATTGGCATGGCTTT-3' (-actin sense primer) and 5'-CACCTTCACCGTTCCAGTTT-3' (-actin antisence primer). The Smad7 primer pairs correspond to the coding region 576–709 and the amplified products are 134 bp in length. The -actin primer pairs correspond to the coding region 1233–1332, and the amplified products are 100 bp in length. Both Smad7 and -actin amplified products have minimal secondary structures, and the melt curve analysis showed no nonspecific amplicon or primer/dimer formation. A QuantiTect CYBRGreen RT-PCR kit (Qiagen Inc.) was used to prepare the real-time RT-PCR reaction mixture. Real-time RT-PCR was performed at 50 °C for 1 h using unique antisense primers for the RT step followed by 45 cycles of amplification using an iCycler iQ Real-Time PCR Detection System (Bio-Rad). The real-time RT-PCR data were simultaneously analyzed using the same system.

Collagen Assays—Collagen assay was performed using the Sircol collagen assay method (Accurate Chemical & Scientific Corp., Westbury, NY) as described previously (5).

Statistical Analysis—The results are presented as means ± S.D. from single experiment that are representative of at least three replicate experiments. Significance between experimental versus control values was calculated using the Student's t test.

	RESULTS

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IL-7 Inhibits TGF--induced COL1A1 and COL3A1 Gene Expression in PFF—To determine whether IL-7 modulates TGF--induced collagen synthesis at the level of regulating COL1A1 and COL3A1 gene expresion, PFF were incubated in medium only, in medium containing acid-activated recombinant TGF-1 (10 ng/ml), or in medium containing TGF-1 plus IL-7 (100 ng/ml). When used at this concentration TGF-1 does not significantly impact fibroblast proliferation at 24 h (5). After a 24-h incubation, cells were harvested for Northern blot analysis using ³²P-labeled oligonucleotide probes that recognize unique human COL1A1 and COL3A1 transcripts. IL-7 significantly reduced TGF--mediated induction of COL1A1 and COL3A1 mRNA levels (Fig. 1).

View larger version (40K): [in this window] [in a new window]   FIG. 1. IL-7 inhibits TGF--induced COL1A1 and COL3A1 mRNA levels. Northern blot analysis of COL1A1 and COL3A1 mRNA levels from PFF incubated in medium alone (lane 1), in medium containing TGF-1 (10 ng/ml, lane 2), or TGF-1 + IL-7 (100 ng/ml, lane 3) for 24 h. Housekeeping gene -actin was used as controls for equal loading.

View larger version (17K): [in this window] [in a new window]   FIG. 2. IL-7 inhibits, while TGF- stimulates, PKC- activity. PKC- activity assays with [-32P]ATP and histone H1 as an external substrate in PFF and NF. The PKC- activity was determined by the amount of 32P-histone H1 produced as detected by autoradiography following SDS-PAGE electrophoresis. Lane 1, medium alone; lane 2, IL-7 (100 ng/ml, lane 2); lane 3, TGF- (10 ng/ml); lane 4, IL-7 + TGF-.

View larger version (59K): [in this window] [in a new window]   FIG. 3. IL-7 inhibits TGF--mediated phosphorylation of PKC- on Thr-505 and Ser-645 in PFF. PKC- phosphorylation patterns in response to IL-7 and TGF- in NF and PFF were determined by Western blot analysis using specific monoclonal antibodies. PFF and NF were incubated in the following conditions: medium only, IL-7 (100 ng/ml), TGF- (10 ng/ml), and IL-7 + TGF- at 37 °C for 1 h. M, molecular weight marker. TGF- and IL-7 had no effect on total PKC- protein levels in both NF and PFF. TGF- significantly increased the phosphorylated levels of PKC--[pThr505] and PKC--[Ser645], and IL-7 inhibited this event in PFF. PKC--[pTyr311] levels did not change when exposed to TGF- or IL-7 in PFF. In contrast, the phosphorylated PKC- levels in NF were not influented by TGF- or IL-7.

with Specific siRNA Significantly Increased Smad7 mRNA Levels and, in Parallel, Reduced TGF--mediated Collagen Synthesis in PFF—

View larger version (54K): [in this window] [in a new window]   FIG. 4. Inhibition of PKC- with specific siRNA significantly increased Smad7 mRNA levels and in parallel, reduced TGF--mediated collagen synthesis in PFF. A, PKC- siRNA effectively inhibited PKC- as demonstrated by Western blot analysis. Preliminary studies showed that 2 µg of PKC- siRNA premixed with the transfectant in a ratio of 1:8 provided optimal gene silencing effect without significant toxicity to the cells. B, inhibition of PKC- with siRNA resulted in an increase in Smad7 mRNA levels by real-time RT-PCR. The left panel is a representative histogram of real-time RT-PCR. Red line, solvent only; brown line, TGF- (10 ng/ml); blue line, TGF- (10 ng/ml) + PKC- siRNA. A left shift of threshold cycle from the red line (solvent only) to the brown line (TGF-) in NF indicated an increase in Smad7 mRNA, while no significant change of threshold cycle was seen in PFF when exposed to TGF-. -Actin was used as controls showing no significant differences. Inhibition of PKC- with siRNA did not induce higher levels of Smad7 mRNA in NF. When PFF were incubated in TGF- plus PKC- siRNA, the threshold cycle changed from the brown line (TGF- only) to the blue line (TGF- + PKC- siRNA) in PFF, indicating that inhibition of PKC- appeared to restore the capacity of TGF- to induce Smad7 in PFF. The right panel shows relative values of Smad7 mRNA levels in bar graph form in NF (n = 2) and PFF (n = 3). *, p < 0.05; **, p < 0.01. C, inhibition of PKC- led to significant reduction in collagen synthesis. Parallel studies were conducted in PFF to determine collagen levels. Again, cells were cultured in medium alone, in medium containing TGF-1 (10 ng/ml), or in combination of TGF- plus PKC- siRNA for 24 h. The collagen content was determined using the Sircol collagen assay kit (Accurate). **, p < 0.01; ***, p < 0.001.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

We reported previously that IL-7 has the capacity to block TGF- signaling by up-regulation of Smad7, a major inhibitory member of the Smad family. In vitro, IL-7 inhibits fibroblast collagen deposition in a Smad-7-dependent manner (5). In vivo, IL-7 limits pulmonary fibrosis (5). Because collagen types I and III are major components of extracellular matrix in pulmonary fibrosis (2, 3), we first investigated the effect of IL-7 on TGF--mediated induction of COL1A1 and COL3A1 gene expression in PFF. Consistent with a marked reduction in collagen synthesis as previously reported, the current results show that IL-7 inhibits TGF--mediated induction of COL1A1 and COL3A1 gene expression in PFF. Thus, IL-7 inhibits TGF--mediated collagen synthesis at both mRNA and protein levels.

PKC- is a member of the PKC family of serine-threonine kinases, which play important roles in signaling for various cytokine receptors. Specifically relevant to our current study, the Smad cascade and PKC- mediate TGF-1-induced target gene expression in a variety of cell types (1, 6). Previous studies indicate that inhibition of PKC- results in marked reduction in TGF--induced COL1A1 and COL3A1 mRNA expression (13), suggesting that PKC- may play an important role in the regulation of TGF--mediated collagen synthesis. In the current study, we have shown that TGF- stimulates, while IL-7 inhibits, PKC- activity in PFF. These opposing effects of TGF- and IL-7 on PKC- correlate well with our previously published work; TGF- stimulates, while IL-7 inhibits, collagen synthesis in PFF. TGF- stimulates phosphorylation of PKC- at Ser-645 and Thr-505, while IL-7 inhibits this process in PFF. TGF- receptors have intrinsic serine-threonine kinase activity, which serves as a key component in the activation of intracellular TGF- signaling (1, 9). Our results suggest that IL-7 may inhibit TGF--mediated PKC- phosphorylation of Ser-645 and Thr-505 by interfering with TGF- receptor intrinsic kinase activity in cells in which PKC- is a downstream target of TGF- receptor serine-threonine kinases. In addition to phosphorylation on Ser-645 and Thr-505, PKC- can also be phosphorylated by various tyrosine kinases including Fyn, Src, Lyn, Lck, and Abl (1, 9). Our results show that TGF- and IL-7 have no effect on PKC- phosphorylation at Tyr-311 in both PFF and NF. Thus, Tyr-311 phosphorylation may not be required for PKC- activity in human pulmonary fibroblasts.

We (5, 14) and others (15–17) have reported marked phenotypic and functional differences between PFF and NF. These differences have been demonstrated at multiple levels including TGF- receptor expression, expression of cell surface receptors or signal transduction mediators, regulation of TGF- signaling, and response to cytokines or other stimulators. Normal fibroblasts have the capacity to produce TGF- in response to a variety of stimuli. This production of TGF- then serves to control and mediate processes such as wound repair. However, following TGF- production, regulatory mechanisms must also be initiated to limit TGF- signaling and avoid, for example, uncontrolled collagen production and fibrogenesis. Thus, exposure of normal cells to TGF- leads to the rapid induction of Smad7 mRNA expression. In the current study, Smad7 mRNA levels rapidly increased in response to TGF- stimulation in NF, while no significant differences were observed in PFF. The results suggest that the normal negative feedback regulatory mechanism for TGF- signaling may be impaired in PFF. Thus, NF are endowed with balanced fibrogenic and antifibrogenic regulatory mechanisms and appear to be resistant to aberrant signals seen in pulmonary fibrosis. In comparison, PFF have a fibrogenic phenotype. Importantly, inhibition of PKC- (>95% inhibition) with specific siRNA significantly increased Smad7 mRNA levels and, in parallel, reduced TGF--mediated collagen synthesis in PFF. The results suggest that the inhibition of PKC- may at least partially restore the negative feedback of TGF- in PFF by facilitating an increase in Smad7.

IL-7 is a cytokine within the IL-2 receptor common chain (IL-2R(c) superfamily (18). IL-7 receptor (IL-7R/(c)) is comprised of a unique chain (IL-7R) and a common (IL-7R) subunit shared by other cytokine receptors including IL-2, IL-4, IL-9, and IL-15 (19). Activation of the JAK/STAT pathway has been implicated in IL-7 signaling (5, 20). Specifically, IL-7 is known to activate JAK1 through the ligand-specific IL-7R chain and subsequently activate STATs, while the shared IL-7R(c) subunit cross-linking by ligands activates JAK3, an upstream activator of a variety of signal transduction pathways (21). In vitro, IL-7 has the capacity to inhibit fibroblast TGF- signaling in a JAK1/STAT1-dependent manner. In vivo, IL-7 decreases bleomycin-induced pulmonary fibrosis. Here we show for the first time that the counter-regulatory roles mediated by IL-7 and TGF- in pulmonary fibroblast Smad7 expression and collagen synthesis are PKC--dependent. PKC- may play a critical role in the pathogenesis of pulmonary fibrosis and serve as a molecular target for therapeutic intervention. The development of pathogenesis-based therapy for pulmonary fibrosis offers an entirely new avenue for therapeutic intervention.

	FOOTNOTES

 
^* This work was supported by National Institutes of Health (NIH) Grant P50 CA90388 (The UCLA Specialized Program of Research Excellence in Lung Cancer); NIH Grants R01 CA085686 [GenBank] (to S. M. D.), P50 HL67665 (to R. M. S. and M. P. K.), and P01 HL 03906 (to R. M. S. and M. P. K.); the American Lung Association; the Medical Research Funds from the Department of Veteran Affairs; the Research Enhancement Award Program; and the Tobacco-related Disease Research Program of the University of California. 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.

^|| To whom correspondence should be addressed. Tel.: 310-268-4420; Fax: 310-268-4164; E-mail: minhuang{at}mednet.ucla.edu.

¹ The abbreviations used are: TGF-, transforming growth factor-; PKC-, protein kinase C-; IL-7, interleukin-7; IPF, idiopathic pulmonary fibrosis; PFF, pulmonary fibrosis fibroblasts; NF, normal fibroblasts; siRNA, small inhibitory RNA; RT, reverse transcriptase.

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