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J. Biol. Chem., Vol. 276, Issue 10, 7218-7224, March 9, 2001

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Transporters on Demand

INTRAHEPATIC POOLS OF CANALICULAR ATP BINDING CASSETTE TRANSPORTERS IN RAT LIVER^*

Helmut Kipp, Nipaporn Pichetshote, and Irwin M. Arias^§

From the Tufts University School of Medicine, Department of Physiology, Boston, Massachusetts 02111

Received for publication, August 25, 2000, and in revised form, December 1, 2000

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

ABC transporter trafficking in rat liver induced by cAMP or taurocholate and [³⁵S]methionine metabolic labeling followed by subcellular fractionation were used to identify and characterize intrahepatic pools of ABC transporters. ABC transporter trafficking induced by cAMP or taurocholate is a physiologic response to a temporal demand for increased bile secretion. Administration of cAMP or taurocholate to rats increased amounts of SPGP, MDR1, and MDR2 in the bile canalicular membrane by 3-fold; these effects abated after 6 h and were insensitive to prior treatment of rats with cycloheximide. Half-lives of ABC transporters were 5 days, which suggests cycling of ABC transporters between canalicular membrane and intrahepatic sites before degradation. In vivo [³⁵S]methionine labeling of rats followed by immunoprecipitation of (sister of P-glycoprotein) (SPGP) from subcellular liver fractions revealed a steady state distribution after 20 h of SPGP between canalicular membrane and a combined endosomal fraction. After mobilization of transporters from intrahepatic sites with cAMP or taurocholate, a significant increase in the amount of ABC transporters in canalicular membrane vesicles was observed, whereas the decrease in the combined endosomal fraction remained below detection limits in Western blots. This observation is in accordance with relatively large intracellular ABC transporter pools compared with the amount present in the bile canalicular membrane. Furthermore, trafficking of newly synthesized SPGP through intrahepatic sites was accelerated by additional administration of cAMP but not by taurocholate, indicating two distinct intrahepatic pools. Our data indicate that ABC transporters cycle between the bile canaliculus and at least two large intrahepatic ABC transporter pools, one of which is mobilized to the canalicular membrane by cAMP and the other, by taurocholate. In parallel to regulation of other membrane transporters, we propose that the "cAMP-pool" in hepatocytes corresponds to a recycling endosome, whereas recruitment from the "taurocholate-pool" involves a hepatocyte-specific mechanism.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

The bile canalicular membrane of the mammalian hepatocyte contains several primary active transporters that couple ATP hydrolysis to the transport of specific substrates into the bile canaliculus (1-4). These transporters are members of the superfamily of ATP binding cassette (ABC)¹ membrane transport proteins (5) and currently include P-glycoprotein (MDR1) for organic cations (6), MDR2 for phosphatidylcholine translocation (7, 8), sister of P-glycoprotein (SPGP), the canalicular bile salt export pump (BSEP) (9), and MRP2 for non-bile acid organic anions (10).

Recent studies indicate that the amount of each ABC transporter in the canalicular membrane is regulated by the physiological demand to secrete bile acids. Intravenous administration to rats of dibutyryl-cAMP (Bt₂cAMP) or taurocholate (TC) rapidly and selectively increased the functional activity and amount of each ABC transporter in the canalicular membrane; these effects were inhibited by prior administration of colchicine, which disrupts microtubules (11), and Wortmannin, which inhibits phosphatidylinositol 3-kinase (12). These observations indicate that an intracellular microtubule-dependent transport mechanism, which is sensitive to active phosphatidylinositol 3-kinase, is required for trafficking of ABC transporters to the canalicular membrane. ATP-dependent transport activity of SPGP and MRP2 within the bile canalicular membrane requires active phosphatidylinositol 3-kinase and is regulated by 3'-phosphorinositide products of phosphatidylinositol 3-kinase (13).

ABC transporters are essential for biliary secretion in mammalian liver, and their amounts and activities in the canalicular membrane are tightly regulated. Inherited defects in SPGP and MRP2 proteins result in familial intrahepatic cholestasis (for review, see Ref. 14). Therefore, defects in trafficking and regulation of ABC transporters may result in insufficient amounts or activity of ABC transporters in the bile canalicular membrane, the consequences of which are impaired bile secretion and cholestasis (15).

The increase in the content of ABC transporters in the canalicular membrane after administration of Bt₂cAMP or TC in vivo (11) and in isolated perfused rat liver (12, 13) occurred within minutes after the administration of the effectors. These observations suggest that the increment in canalicular ABC transporters is likely to represent recruitment from pre-existing intrahepatic pools rather than from enhanced transcription or translation. Furthermore, the simultaneous administration of Bt₂cAMP and TC resulted in additive rather than alternative effects (11). These observations suggest that Bt₂cAMP and TC recruit ABC transporters to the canalicular membrane from different intrahepatic pools. Moreover, investigations of Golgi-to-bile canaliculus pathways of newly synthesized ABC transporters (16, 17) also suggest that SPGP, in particular, is sequestered in intrahepatic pools before reaching the bile canalicular plasma membrane. The present report concerns biochemical identification and characterization of these intrahepatic ABC transporter pools and identification of possible mechanisms by which ABC transporters are made available to the canalicular membrane.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Materials-- Expre³⁵S³⁵S protein label was supplied by PerkinElmer Life Sciences. All other chemicals were of highest purity available and were purchased from Sigma. Monoclonal antibody C219 (anti-MDR1/MDR2) was from Centocor (Malvern, PA). Polyclonal anti-SPGP antibody LVT90 was developed in our laboratory (15). Polyclonal anti-cCAM105 antibody was a gift from S. H. Lin (Houston, TX). Antibodies against Rab proteins were from Santa Cruz Biotechnology.

Miscellaneous Methods-- Young adult male Harlan Sprague-Dawley rats (300-350 g) kept on a standard diet were used for preparation of liver subcellular fractions. In some experiments, rats were pretreated by intravenous injection with Bt₂cAMP (20 µmol/kg) or TC (50 µmol/kg) dissolved in 1 ml of PBS for the indicated time periods. In control experiments, rats received 1 ml of PBS. Further experimental details are stated in the figure legends. Preparation and characteristics of rat liver canalicular membrane vesicles (CMV), sinusoidal/basolateral membrane vesicles (SMV), and Golgi membranes were described previously (16, 18, 19). A combined endosomal fraction (CEF) from rat liver was prepared using the protocol of Khan et al. (20). Metabolic [³⁵S]methionine labeling and immunoprecipitation from subcellular rat liver fractions were performed as described earlier (16). Proteins were separated by SDS-PAGE according to Laemmli (21). For Western blotting, polypeptides were electrotransferred (22) on nitrocellulose membranes (Schleicher & Schuell) or polyvinylidene difluoride membrane (Milipore) for the Rab proteins. Antibodies were detected by incubation with horseradish peroxidase-conjugated secondary antibodies followed by detection with an enhanced chemiluminescence system from PerkinElmer Life Sciences. The method of Lowry et al. (23) was used for protein measurements with bovine serum albumin as standard.

	RESULTS

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Bt₂cAMP and TC Transiently Increase the Canalicular Amount of ABC Transporters-- Gatmaitan et al. (11) demonstrate that intravenous injection of rats with Bt₂cAMP or TC increased the amount of canalicular proteins in the bile canalicular membrane. To determine the duration and magnitude of the response to Bt₂cAMP and TC administration, we investigated the time courses of these effects. Groups of rats were injected with either Bt₂cAMP (20 µmol/kg) or TC (50 µmol/kg) for various time periods, and canalicular amounts of ABC transporters were determined in CMVs by Western blotting (Fig. 1). We demonstrated earlier that monoclonal C219 antibody is specific for rat MDR1 and MDR2 and that polyclonal LVT90 antibody is specific for SPGP (16). After treatment with Bt₂cAMP, an increase in MDR1, MDR2, and SPGP in CMVs was observed after 15 min; the effect peaked at 45 min to 4 h and disappeared after 6 h. TC treatment resulted in a significant increase in MDR1, MDR2, and SPGP after 15 min; the effect peaked at 45 to 90 min and then declined to the basal level after 4 h. From three sets of independent experiments, the maximal increase in the amount of ABC transporters in the canalicular membrane was 3.6 ± 0.9-fold after stimulation with Bt₂cAMP and 2.7 ± 0.7-fold after treatment with TC.

View larger version (28K): [in this window] [in a new window]   Fig. 1.   Bt2cAMP and TC temporarily increase canalicular amount of ABC transporters. Groups of rats were injected with Bt2cAMP (20 µmol/kg) or TC (50 µmol/kg) in PBS, and livers were excised after the indicated time points for the preparation of CMVs. Equal amounts of CMV proteins (20 µg/lane) were separated by SDS-PAGE, blotted onto nitrocellulose membrane, and probed with LVT90 (SPGP) and C219 (MDR1/MDR2) antibodies. A control group of rats received only injection with PBS. Panels A and C show representative results observed in three independent sets of rats. Panels B and D show densitometric quantitations of Western blots from three independent sets of rats (mean values ± S.D., n = 3) with TC (mean values ± S.D., n = 3). The asterisk indicates values significantly different from control using Student's t test (p < 0.05).

Onset and duration of the Bt₂cAMP and TC effects probably depend on the dose of the injected drug, which has not been investigated in detail. However, the increase in ABC transporter amounts in the bile canaliculus caused by Bt₂cAMP or TC is transient, which prompts two questions: Where do the additional ABC transporters originate from? Where do they go after the effects have abated?

TC and cAMP Effects Are Independent of de Novo Protein Synthesis-- Additional ABC transporters in the bile canaliculus upon stimulation with Bt₂cAMP or TC could theoretically result from enhanced protein biosynthesis and/or recruitment of transporters from pre-existing intracellular pools. To discriminate between these possibilities, we determined whether the increase in ABC transporters in the bile canaliculus remained when protein synthesis was inhibited. Protein biosynthesis was efficiently blocked by intraperitoneal injection of rats with cycloheximide (5 mg/kg) for 30 min. Pretreatment with cycloheximide completely abolished metabolic labeling with [³⁵S]methionine of proteins in CMVs. This was demonstrated by detection of ³⁵S-labeled proteins in CMVs with a scintillation counter and of radiolabeled proteins using PhosphorImager after separation of CMV proteins by SDS-PAGE (Fig. 2).

View larger version (35K): [in this window] [in a new window]   Fig. 2.   Cycloheximide efficiently inhibits protein biosynthesis. To establish the effectiveness of cycloheximide (CHX) in blocking protein biosynthesis in vivo, a rat was treated with an intraperitoneal injection of cycloheximide (5 mg/kg) for 30 min before metabolic labeling with [35S]methionine for 2 h. CMVs were prepared, and radioactivity was determined from an aliquot by liquid scintillation counting (A). Furthermore, an aliquot of CMVs was separated by SDS-PAGE and stained with Coomassie (B), and radioactivity was then detected by phosphorimaging (C). The results were compared with CMVs from a rat without cycloheximide pretreatment. The results shown were established in a single experiment; error bars indicate S.D. from three replica.

Rats were injected intraperitonally with cycloheximide for 30 min followed by intravenous injection of either Bt₂cAMP or TC for 1 h. CMVs were then prepared, and proteins from rat liver homogenate and CMVs were separated by SDS-PAGE. The amount of ABC transporters in both preparations was quantified by Western blotting with C219 (MDR1, MDR2) and LVT90 (SPGP) antibodies and compared with control experiments (Fig. 3).

View larger version (36K): [in this window] [in a new window]   Fig. 3.   TC and cAMP effects are independent of de novo protein synthesis. Rats were injected intraperitonally with cycloheximide (CHX) (5 mg/kg) for 30 min followed by intravenous injection of either Bt2cAMP (20 µmol/kg) or TC (50 µmol/kg) for 1 h. In control experiments, rats received an injection with PBS. Equal amounts of homogenate (HOM, A and B) (50 µg/lane) and CMVs (C and D) (20 µg/lane) were separated by SDS-PAGE, blotted onto nitrocellulose membrane, and probed with LVT90 (SPGP) and C219 (MDR1/MDR2) antibodies. Panels A and C show representative results observed in three independent sets of rats. Panels B and D show densitometric quantitations of Western blots from three independent sets of rats (mean values ± S.D., n = 3). The asterisk indicates values significantly different from control using Student's t test (p < 0.05).

Cycloheximide inhibits protein biosynthesis; however, in some instances cycloheximide can also cause superinduction of proteins (24, 25). In rat liver homogenate no significant change in the amount of ABC transporters was observed after pretreatment of rats with cycloheximide, Bt₂cAMP, and TC in various combinations (Figs. 3, A and B). These data indicate that superinduction of proteins by cycloheximide is not a concern in our study regarding ABC transporters. The total amount of SPGP, MDR1, and MDR2 in rat liver remained constant after administration of cycloheximide, Bt₂cAMP, and TC.

Pretreatment of rats with cycloheximide for 30 min had no effect on the basal protein amount of MDR1, MDR2, and SPGP in CMVs. Cycloheximide pretreatment did not reduce the increase in ABC transporters in the bile canaliculus in response to Bt₂cAMP or TC. Regardless of prior cycloheximide administration, Bt₂cAMP or TC significantly increased the canalicular content of MDR1, MDR2, and SPGP when compared with control animals (Figs. 3, C and D). These experiments demonstrate that additional ABC transporters in the bile canalicular membrane after stimulation with Bt₂cAMP or TC do not result from enhanced translation but from a redistribution between intrahepatic ABC transporter pools and the bile canalicular membrane.

Half-lives of Canalicular ABC Transporters-- Where do the canalicular ABC transporters go after peak stimulation by Bt₂cAMP or TC and their amounts in the bile canalicular membrane return to basal levels? Two possible scenarios were considered as follows. ABC transporters either return to intrahepatic sites, or in parallel with other canalicular protein receptors, they are degraded. The latter presumably should be manifested by relatively short half-lives for canalicular ABC transporters. Therefore, we determined the half-lives of the canalicular ABC transporters and compared the results to previously established half-lives of other hepatocyte plasma membrane proteins.

A group of rats was labeled by intravenous injection with [³⁵S]methionine for 1, 3, 5, 8, and 10 days (without chase), and the content of newly synthesized MDR1, MDR2, and SPGP was determined by immunoprecipitation from CMVs and homogenate. The half-life of cCAM105 was also determined as a control. Protein half-lives were determined from semi-logarithmic plots of ³⁵S intensity versus labeling time (Fig. 4). As observed earlier (16), MDR1 and MDR2 could not be immunoprecipitated with C219 antibody from liver homogenate, probably due to low abundance of the antigens.

View larger version (38K): [in this window] [in a new window]   Fig. 4.   Half-lives of canalicular proteins. Rats were metabolically labeled by intravenous injection with [35S]methionine (5 mCi) for 1, 3, 5, 8, and 10 days. cCAM105 (A) and MDR1/MDR2 and SPGP (C) were then immunoprecipitated from liver homogenate (HOM) and CMVs. Immunoprecipitates were separated by SDS-PAGE, and radiolabeled bands were detected and quantified by phosphorimaging. Half-lives of the proteins were estimated from semi-logarithmic plots (B and D) of the relative 35S intensity (highest values equal 100) versus labeling time. Assuming first order decay, data points were fitted linearly by the least square method. Determined half-lives are: cCAM105, 5 days; MDR1 and MDR2, 5 days; SPGP, 4 days (CMVs) and 6 days (HOM). The half-lives were established with one set of five rats.

Assuming first order decay, cCAM105 had an apparent half-life of 5 days as measured in homogenates and CMVs, which corresponds to an earlier published report (26). A 5-day half-life was also determined for MDR1 and MDR2 in CMVs. For SPGP, a half-life of 4 days was measured from CMVs and 6 days from homogenate. It is not clear why the apparent half-lives differ when determined from the two preparations. However, it has been observed before that the apparent half-lives of hepatic proteins are shorter when determined from plasma membranes as compared with results in homogenates (26).

The half-lives of several hepatocyte plasma membrane proteins are presented in Table I and were obtained from metabolic studies using radiolabeled amino acids. Except for nucleotide pyrophosphatase and the polymeric IgA receptor, which have short half-lives, all other hepatic plasma membrane proteins previously investigated have half-lives of 2-9 days. The short half-life of the polymeric IgA receptor is accounted for by extensive loss into the bile (26). Since it is difficult to prevent long term label reincorporation in vivo (26, 29), the data probably represent upper limits. Similar to other hepatic plasma membrane proteins (Table I), canalicular SPGP, MDR1, and MDR2 have relatively long half-lives (t_1/2 > 1 day) and are likely to undergo lysosomal degradation (31).

Trafficking of ABC transporters from intrahepatic sites to the bile canalicular membrane is physiologic and results from increased need to secrete bile. Therefore, we postulate that canalicular ABC transporters cycle between the apical membrane and intrahepatic sites prior to undergoing degradation.

Large Amounts of SPGP Reside in Intracellular Pools-- A CEF from rat liver was prepared (20) to investigate the dynamics and steady state levels of SPGP in intrahepatic pools. CEFs, prepared by centrifugation of a microsomal fraction of rat liver on a discontinuous sucrose gradient, are highly enriched in endosomal markers Rab5 (early endosomes) and Rab11 (apical recycling endosomes) (32) as compared with homogenates and CMV and SMV plasma membrane subfractions (Fig. 5).

View larger version (33K): [in this window] [in a new window]   Fig. 5.   Rab 5 and Rab 11 are highly enriched in a CEF from rat liver. Rat liver homogenate (HOM), CEF, CMVs, and SMVs were separated by SDS-PAGE (10 µg of protein of each fraction), blotted onto a polyvinylidene difluoride membrane, and probed with anti-Rab5 (early endosomes) and anti-Rab11 (apical recycling endosomes) antibodies.

In a recent paper (16), we described trafficking of newly synthesized SPGP by investigating the kinetics of [³⁵S]methionine-labeled SPGP in liver homogenate, Golgi membranes, CMVs, and SMVs. SPGP was never observed in SMVs, indicating nontranscytotic targeting. Furthermore, in study of SPGP trafficking, there was a 1.5-h lag between passage through Golgi and arrival at the canalicular membrane, which suggests transient sequestration in intrahepatic sites. We expanded this experiment to include CEF. Trafficking of newly synthesized SPGP after pulse-chase labeling with [³⁵S]methionine through Golgi membranes, CEF, and CMVs is shown in Fig. 6.

View larger version (36K): [in this window] [in a new window]   Fig. 6.   Newly synthesized SPGP is targeted through an endosomal compartment. Rats were pulse-labeled for 15 min with [35S]methionine (5 mCi) and then chased with unlabeled methionine for 15 and 30 min and 1, 2, 3, and 20 h, respectively. SPGP was then immunoprecipitated from Golgi membranes, CEF, and CMVs. Immunoprecipitates were separated by SDS-PAGE, and [35S]SPGP was detected by phosphorimaging. Panel A shows representative results observed in three independent sets of rats; arrowheads indicate the position of mature antigens. To establish the kinetics of newly synthesized SPGP trafficking through cellular compartments (squares, Golgi; diamonds, CEF; circles, CMV), intensities of [35S]SPGP bands were quantified by phosphorimaging. The relative intensity (highest reading in each fraction equals 100) was plotted versus labeling time (B); mean values ± S.D., n = 3.

Radiolabeled SPGP peaked in Golgi membranes after a chase time of 30 min and thereafter was virtually absent from the Golgi, indicating that processing and passage of SPGP through Golgi is complete after 30-60 min. SPGP peaked in CEF at 1 h and, after a chase time of 2 h, first appeared in CMVs. These experiments demonstrate that newly synthesized SPGP is targeted through an endosomal compartment before reaching the bile canalicular membrane. Furthermore, SPGP is not completely transferred from CEF, and a significant amount of SPGP remains in the endosomal fraction. These results suggest a distribution of SPGP between canalicular membrane and intracellular pools (2- and 3-h chase). This was also observed after a chase time of 20 h, which presumably represents steady state distribution of SPGP between the bile canaliculus and intracellular pools under basal conditions.

Immunoblots were used to determine the distribution of SPGP and MDR1/MDR2 between CMVs and CEF under steady state conditions and after induction of trafficking with Bt₂cAMP or TC (Fig. 7). Administration to rats of Bt₂cAMP or TC for 1 h significantly increased the amounts of SPGP and MDR1/MDR2 in the canalicular membrane, whereas the amounts in liver homogenate remained constant. These data suggest a redistribution of existing ABC transporters between intracellular pools and the canalicular membrane upon stimulation with Bt₂cAMP and TC. Surprisingly, no decrease in the ABC transporter amount could be detected in CEF; the amount of SPGP, MDR1, and MDR2 remained constant after stimulation with Bt₂cAMP and TC. These observations can be best explained by a large intrahepatic pool of ABC transporters, only a small portion of which is present in the bile canalicular membrane. In this scenario, a small portion of ABC transporters trafficking from a large endosomal pool to a small bile canalicular pool results in significantly increased amount of ABC transporters in CMVs, whereas any decrease in ABC transporter amount in CEF remained below the detection limit.

View larger version (51K): [in this window] [in a new window]   Fig. 7.   Under basal conditions the major amount of ABC transporters resides in intrahepatic pools. Rats were injected with Bt2cAMP (20 µmol/kg) or TC (50 µmol/kg), and livers were excised after 1 h for the preparation of CMVs and CEF. A control group of rats received only injection with PBS. Equal amounts of homogenate (HOM) 50 µg/lane), CMVs (20 µg/lane), and CEF proteins (20 µg/lane) were separated by SDS-PAGE, blotted onto nitrocellulose, and probed with LVT90 (SPGP) and C219 (MDR1/MDR2) antibodies. Panels A and C show representative results observed in three independent sets of rats. WB, Western blot. Panels B and D show densitometric quantitations of Western blots from three independent sets of rats (mean values ± S.D., n = 3). The asterisk indicates values significantly different from control using Student's t test (p < 0.05).

Targeting of Newly Synthesized SPGP to the Bile Canaliculus Is Accelerated by Bt₂cAMP But Not by TC-- Newly synthesized SPGP is targeted through intrahepatic sites before reaching the bile canalicular membrane. This was concluded from the 1.5-h lag time between passage through Golgi and arrival at the hepatocyte apical pole (16) and was confirmed by [³⁵S]methionine metabolic pulse-chase labeling of a CEF from rat liver (Fig. 6). The pattern of ABC transporter trafficking after injection of rats with Bt₂cAMP or TC also suggests the existence of intrahepatic pools. The two approaches were combined to determine whether intrahepatic SPGP pools, in which newly synthesized SPGP is sequestered before reaching the bile canaliculus, is also mobilized by Bt₂cAMP and/or TC. Typically [³⁵S]SPGP is first detected in CMVs after 2 h in metabolic labeling studies. Therefore, we determined whether [³⁵S]SPGP can be detected in CMVs after 1 h of labeling after additional administration of Bt₂cAMP or TC (Fig. 8).

View larger version (30K): [in this window] [in a new window]   Fig. 8.   Membrane targeting of newly synthesized SPGP is accelerated by cAMP but not by TC. Rats were pulse-labeled for 15 min with [35S]methionine (5 mCi) and then chased with unlabeled methionine for 1 h. At a chase time of 30 min, rats received an intravenous injection of PBS (control), Bt2cAMP (20 µmol/kg), or TC (50 µmol/kg). CMVs were prepared from the rat livers from which SPGP was immunoprecipitated. A, immunoprecipitates (IP) were separated by SDS-PAGE and [35S]SPGP detected by phosphorimaging (a typical result, observed in three independent sets of three rats is shown). B, equal protein amounts (20 µg) of the same CMV preparations were separated by SDS-PAGE, blotted onto nitrocellulose membrane, and probed with anti-SPGP antibody. WB, Western blot. C, Western blots from three independent sets were quantitated with a laser densitometer and compiled; mean values ± S.D., n = 3. The asterisk indicates values significantly different from control using Student's t test (p < 0.05).

As demonstrated before, treatment of rats with Bt₂cAMP or TC for 30 min significantly increased the steady state amount of SPGP in CMVs. However, accelerated trafficking of newly synthesized SPGP to the bile canalicular membrane after 1 h was observed only when rats were pretreated with Bt₂cAMP. Pretreatment with TC did not accelerate Golgi-to-bile canaliculus trafficking of newly synthesized SPGP. Altered schedules for TC administration 15 or 45 min after metabolic labeling also did not accelerate [³⁵S]SPGP trafficking to the canalicular membrane (data not shown). Thus, trafficking of newly synthesized SPGP through intrahepatic pools to the bile canalicular membrane was accelerated by cAMP but not by TC.

	DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS DISCUSSION REFERENCES

Previous morphological studies in rats rendered cholestatic by bile duct ligation (33), phalloidin (34), or lipopolysaccharide (35) suggest that MRP2 and SPGP may traffic from the bile canaliculus to intracellular sites. In addition, MRP2 (35) and SPGP (9) were observed by immunogold staining and electron microscopy in undefined vesicular structures that were distinct from the bile canaliculus.

The present study demonstrates that selective increase in ABC transporters in the canalicular membrane after stimulation with cAMP or TC is independent of protein de novo synthesis, indicating that additional transporters, upon stimulation, are recruited from pre-existing intrahepatic pools. Stimulation by the second messenger, cAMP, and the SPGP substrate, TC, probably mimic naturally occurring processes. The cAMP and TC effects are transient, and the half-lives of SPGP, MDR1, and MDR2 are not significantly shorter than those of other hepatic plasma membrane proteins, which suggests that ABC transporters cycle between intrahepatic pools and the canalicular membrane. The steady state distribution of SPGP between intrahepatic pools and canalicular membrane is probably regulated by cAMP and TC depending on the physiological demand to secrete bile.

Previous studies (11) indicate that the increasing effects of Bt₂cAMP and TC in bile canalicular ABC transporter amount are additive rather than alternative, which suggests the presence of at least two distinct intrahepatic pools of ABC transporters, one of which is mobilized to the canalicular membrane by Bt₂cAMP (cAMP pool) and the other by TC (TC-pool). We here demonstrate that targeting of newly synthesized SPGP through intrahepatic sites to the bile canalicular membrane is accelerated by Bt₂cAMP but not by TC. This observation supports the hypothesis of two distinct intrahepatic pools of SPGP. After passage through Golgi, SPGP accumulates in an intrahepatic cAMP pool and later equilibrates with the TC pool. Whether equilibration of newly synthesized SPGP with the TC pool occurs from the bile canalicular membrane or the cAMP pool remains unclear. A tentative model for intrahepatic pathways of ABC transporters is shown in Fig. 9. Newly synthesized MDR1 and MDR2 bypass the intracellular pools on their journey to the bile canaliculus (16, 17). However, at steady state levels, MDR1 and MDR2 are also mobilized to the bile canalicular membrane by Bt₂cAMP and TC, indicating that these ABC transporters also equilibrate with intrahepatic pools after reaching the bile canalicular membrane.

View larger version (20K): [in this window] [in a new window]   Fig. 9.   Tentative model for ABC transporter trafficking in rat hepatocytes. Dashed arrows indicate possible pathways of ABC transporters from the TC pool. See text for explanation.

Using metabolic pulse-chase [³⁵S]methionine labeling, a CEF was identified to be the site at which newly synthesized SPGP accumulates before being targeted to the bile canalicular membrane. After newly synthesized SPGP reached the bile canalicular membrane, a significant amount remained in CEF 20 h after labeling, suggesting steady state distribution of SPGP between canalicular membrane and intrahepatic pools. Since absolute amounts of ABC transporters in the prepared membrane fractions are not known nor how much of the total amount in the rat hepatocyte they represent, precise calculation of the intrahepatic/canalicular ratio exceeds the limits of these experiments. For MRP2, this ratio has been calculated to be ~1:1 by quantitation of immunogold-stained MRP2 in electron microscopy (35) in rat liver under basal conditions. Investigation of ABC transporters by immunoblots at steady state levels revealed that, after stimulation with Bt₂cAMP or TC, the amounts of MDR1, MDR2, and SPGP significantly increased in CMVs, but no change was observed in CEF prepared from the same rat liver. This observation is in accordance with the presence of "large" intrahepatic pools. Under basal conditions, most MDR1, MDR2, and SPGP appears to reside in intrahepatic pools rather than in the canalicular membrane. However, the increase in the amount of ABC transporter in CMVs after stimulation with Bt₂cAMP or TC is ~3-fold for each effector. Taking into account that Bt₂cAMP and TC recruit transporters from different intracellular sources, the intrahepatic pool of ABC transporters is at least 6-times more than the amount present in the bile canalicular membrane. Since this calculation presumes that all intracellular ABC proteins are translocated to the bile canalicular membrane upon stimulation, this number represents a lower limit. Thus, the intrahepatic/canalicular ratio of MDR1, MDR2, and SPGP probably exceeds 6:1.

Upon stimulation with cAMP, trafficking of membrane transporters from intracellular sites to the plasma membrane has been described in several systems, i.e. (i) cystic fibrosis transmembrane regulator (CFTR) channel into the apical surface of rat duodenal villous epithelia (36); (ii) sodium taurocholate cotransport protein (ntcp) in the basolateral membrane of rat hepatocytes (37); (iii) aquaporin-2 water channel into the apical membrane of LLC-PK1 cells, a polarized renal cell line (38); (iv) H⁺/K⁺-ATPase into the apical membrane of gastric parietal cells (39); (v) insulin-responsive glucose transporter 4 into the plasma membrane of rat adipocytes (40). In each of these examples, recruitment of transporters to the plasma membrane from a recycling endosome has been suggested. In particular, trafficking of glucose transporter 4 in rat adipocytes has parallels to that of ABC transporter trafficking in rat hepatocytes. Glucose transporter 4 traffics from distinct intracellular sites to the plasma membrane in response to cAMP and insulin (40). In analogy to these other systems, we propose that cAMP recruits ABC transporters to the bile canalicular membrane from a recycling endosome, whereas the effect of TC appears to be hepatocyte-specific and involves a different mechanism.

The present study demonstrates that a substantial portion of canalicular ABC transporters resides in intracellular pools in hepatocytes and that the transporters can be transiently recruited from different intrahepatic pools to the bile canalicular membrane in response to cAMP and TC. Since ABC transporters are critical for bile formation, the present studies prompt revision of current concepts of bile secretion and raise a question with regard to the mechanism. Do intrahepatic pools of ABC transporters supply additional transporters to the bile canaliculus only to cope with temporarily higher metabolic demand to secrete bile, or are these intracellular ABC transporter pools part of an unidentified more sophisticated bile secretion mechanism? The latter possibility is supported by the finding that intrahepatic pools of MRP2, which also colocalize with SPGP, secrete a MRP2 substrate into intracellular structures (33). A further challenge is the correlation of biochemically observed intrahepatic ABC transporter pools with morphological structures. In this regard, studies in Wif-B cells, a tissue culture model for functionally active, polarized hepatocytes (17, 41, 42), will be a useful tool. Wif-B cells infected with an adenoviral construct containing SPGP tagged with enhanced yellow fluorescent protein showed cycling of SPGP between the canalicular membrane and an intracellular compartment that colocalized with anti-Rab11 (recycling endosomes) antibody immunostaining (43). This project is presently being pursued in our laboratory.

	FOOTNOTES

^* This work was supported by Deutsche Forschungsgemeinschaft Research Grant Ki 640 (to H. K.) and by National Institutes of Health Grants DK35652 (NIDDK) and 30DK34928 (Digestive Disease Center, NIDDK) (to I. M. A.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Present address: Max-Planck-Institut für molekulare Physiologie, Otto-Hahn-Str. 11, 44227 Dortmund, Germany.

^§ To whom correspondence should be addressed: Tufts University School of Medicine, Dept. of Physiology, 136 Harrison Ave., Boston, MA 02111. Tel.: 617-636-6739; Fax: 617-636-0445; E-mail: irwin. arias{at}tufts.edu.

Published, JBC Papers in Press, December 11, 2000, DOI 10.1074/jbc.M007794200

	ABBREVIATIONS

The abbreviations used are: ABC, ATP binding cassette; Bt₂cAMP, dibutyryl cyclic AMP; CEF, combined endosomal fraction; CMV, canalicular membrane vesicle; SMV, sinusoidal membrane vesicle; TC, taurocholate; PAGE, polyacrylamide gel electrophoresis; PBS, phosphate-buffered saline; SPGP, sister of P-glycoprotein.

	REFERENCES

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