ABSTRACT
Bullous pemphigoid antigen-1 (BPA1) and alpha(6)beta(4)-integrin colocalize at the hemidesmosomes in basal-layer keratinocytes of normal squamous epithelia. The expression of these genes was analyzed during the process of tumor cell invasion and metastasis on frozen sections of head and neck biopsies, and the structural appearance of hemidesmosomes was analyzed by electron microscopy. Despite a diminution of hemidesmosomal structures as revealed by electron microscopy, gene expression of BPA1 and alpha(6)beta(4)-integrins was distinctly upregulated with the onset of invasive growth, demonstrated at the mRNA level by in situ hybridization. The upregulated gene expression extended to the entire proliferative zone of invasive tumors, including the tumor cells which have lost contact with the basement membrane and no longer display hemidesmosomes. The polarized localization of the BPA1 and alpha(6)beta(4) proteins to the basal aspect of the peripheral tumor cells was largely retained in invasive but nonmetastatic lesions, but was lost upon progression to metastatic growth of head and neck squamous cell carcinomas (SCC), in which pericellular staining extended into many tumor cell layers. The results of this study confirm that expression of BPA1 and alpha(6)beta(4)-integrins is elevated in carcinoma cells but is not directed to intact hemidesmosomes. Importantly, this loss of directed localization is an indicator of the capacity to metastasize.
Subject(s)
Antigens, Surface/metabolism , Autoantigens/metabolism , Carcinoma, Squamous Cell/secondary , Carrier Proteins , Collagen/metabolism , Cytoskeletal Proteins , Hemidesmosomes/pathology , Integrins/metabolism , Nerve Tissue Proteins , Non-Fibrillar Collagens , Skin Neoplasms/pathology , Antigens, Surface/genetics , Autoantigens/genetics , Biomarkers, Tumor , Carcinoma, Squamous Cell/metabolism , Carcinoma, Squamous Cell/physiopathology , Collagen/genetics , Dystonin , Gene Expression Regulation, Neoplastic , Hemidesmosomes/metabolism , Hemidesmosomes/ultrastructure , Humans , Integrin alpha6beta4 , Integrins/genetics , Microscopy, Electron , Neoplasm Invasiveness/pathology , Phenotype , RNA, Messenger/analysis , Skin Neoplasms/metabolism , Skin Neoplasms/physiopathology , Up-Regulation/physiology , Collagen Type XVIIABSTRACT
Changes of the intestinal mucosal barrier are considered to play a role in the pathogenesis of inflammatory bowel disease (IBD). Our experiments were designed to identify dysregulation of epithelial junctional molecules in the IBD intestinum and to address whether altered expression of these molecules is a primary event in IBD or a phenomenon secondary to the inflammatory process. Noninflamed and inactively and actively inflamed mucosal tissues from patients with ulcerative colitis or Crohn's disease as well as tissues from control subjects were analyzed for the expression of junctional molecules by different methods. Marked downregulation of junctional proteins and their respective mRNAs was observed in actively inflamed IBD tissues. In IBD tissues with inactive inflammation, only a few junctional molecules such as E-cadherin and alpha-catenin were affected, whereas expression of desmosomal or tight junction-associated proteins appeared almost unchanged. In noninflamed IBD tissues, junctional protein expression was not different from that seen in normal control subjects. In IBD, downregulation of junctional molecule expression is apparently associated with the inflammatory process and does not likely represent a primary phenomenon.
Subject(s)
Colitis, Ulcerative/pathology , Crohn Disease/pathology , Enterocytes/pathology , Intercellular Junctions/pathology , Trans-Activators , Adult , Blotting, Western , Cadherins/analysis , Cadherins/genetics , Colitis, Ulcerative/metabolism , Crohn Disease/metabolism , Cytoskeletal Proteins/analysis , Cytoskeletal Proteins/genetics , Desmoplakins , Enterocytes/chemistry , Female , Fluorescent Antibody Technique , Gene Expression , Humans , Intercellular Junctions/chemistry , Intestinal Mucosa/chemistry , Intestinal Mucosa/pathology , Male , Membrane Proteins/analysis , Membrane Proteins/genetics , Middle Aged , Occludin , Plakophilins , Polymerase Chain Reaction , Proteins/analysis , Proteins/genetics , RNA, Messenger/analysis , alpha Catenin , beta CateninABSTRACT
Simian virus 40 (SV40) is unusual among animal viruses in that it enters cells through caveolae, and the internalized virus accumulates in a smooth endoplasmic reticulum (ER) compartment. Using video-enhanced, dual-colour, live fluorescence microscopy, we show the uptake of individual virus particles in CV-1 cells. After associating with caveolae, SV40 leaves the plasma membrane in small, caveolin-1-containing vesicles. It then enters larger, peripheral organelles with a non-acidic pH. Although rich in caveolin-1, these organelles do not contain markers for endosomes, lysosomes, ER or Golgi, nor do they acquire ligands of clathrin-coated vesicle endocytosis. After several hours in these organelles, SV40 is sorted into tubular, caveolin-free membrane vesicles that move rapidly along microtubules, and is deposited in perinuclear, syntaxin 17-positive, smooth ER organelles. The microtubule-disrupting agent nocodazole inhibits formation and transport of these tubular carriers, and blocks viral infection. Our results demonstrate the existence of a two-step transport pathway from plasma-membrane caveolae, through an intermediate organelle (termed the caveosome), to the ER. This pathway bypasses endosomes and the Golgi complex, and is part of the productive infectious route used by SV40.
Subject(s)
Caveolae/metabolism , Endocytosis , Endoplasmic Reticulum/metabolism , Simian virus 40/metabolism , Animals , Biological Transport , Blotting, Western , Cell Line , Cell Membrane/metabolism , Endosomes/metabolism , Golgi Apparatus/metabolism , Green Fluorescent Proteins , Hydrogen-Ion Concentration , Ligands , Luminescent Proteins/metabolism , Lysosomes/metabolism , Microscopy, Confocal , Microscopy, Fluorescence , Microscopy, Video , Microtubules/metabolism , Nocodazole/pharmacology , Precipitin Tests , Protein Binding , TemperatureABSTRACT
The Dubin-Johnson syndrome is an inherited disorder characterized by conjugated hyperbilirubinemia. The deficient hepatobiliary transport of anionic conjugates is caused by the absence of a functional multidrug-resistance protein 2 (MRP2, symbol ABCC2) from the apical (canalicular) membrane of hepatocytes. Mechanisms underlying this deficiency may include rapid degradation of mutated MRP2 messenger RNA (mRNA) or impaired MRP2 protein maturation and trafficking. We investigated the consequences of the mutation MRP2Delta(R,M), which leads to the loss of 2 amino acids from the second ATP-binding domain of MRP2. The MRP2Delta(R,M) mutation is associated with the absence of the MRP2 glycoprotein from the apical membrane of hepatocytes. Transfection of mutated MRP2 complementary DNA (cDNA) led to an MRP2Delta(R,M) protein that was only core glycosylated, sensitive to endoglycosidase H digestion, and located in the endoplasmic reticulum (ER) of transfected HEK293 and HepG2 cells. This indicated that deletion of Arg1392 and Met1393 leads to impaired maturation and trafficking of the protein from the ER to the Golgi complex. Inhibition of proteasome function resulted in a paranuclear accumulation of the MRP2Delta(R,M) protein, suggesting that proteasomes are involved in the degradation of the mutant protein. This is the first mutation in Dubin-Johnson syndrome shown to cause deficient MRP2 maturation and impaired sorting of this glycoprotein to the apical membrane.
Subject(s)
ATP Binding Cassette Transporter, Subfamily B/metabolism , Gene Deletion , Jaundice, Chronic Idiopathic/genetics , Jaundice, Chronic Idiopathic/metabolism , Membrane Transport Proteins , Multidrug Resistance-Associated Proteins , Protein Processing, Post-Translational , ATP Binding Cassette Transporter, Subfamily B/genetics , Amino Acid Sequence/genetics , Cell Line/metabolism , Cell Membrane/metabolism , Cell Nucleus/metabolism , Cysteine Endopeptidases/physiology , Fluorescent Antibody Technique , Green Fluorescent Proteins , Hepatocytes/metabolism , Hepatocytes/ultrastructure , Humans , Indicators and Reagents , Leupeptins/pharmacology , Luminescent Proteins , Microscopy, Confocal , Microscopy, Immunoelectron , Molecular Sequence Data , Multidrug Resistance-Associated Protein 2 , Multienzyme Complexes/antagonists & inhibitors , Multienzyme Complexes/physiology , Mutation/genetics , Proteasome Endopeptidase Complex , Tissue DistributionABSTRACT
Endothelial cells separate the intra- and extravascular space and regulate transport processes between these compartments. Since intercellular junctions are required for these specific cell functions, the cell-cell contacts in the permanent cell line ECV304 were systematically analyzed and compared with human umbilical vein endothelial cells (HUVECs) in primary culture and with the epithelial Madin Darby Canine Kidney (MDCK) cell line. Filter-grown ECV304 cells generate a distinct electrical resistance and a permeability barrier between cell culture compartments. Electron microscopy of ECV304 cells revealed lateral membrane interdigitations, typically found in endothelial cells in vivo, with direct membrane contact sites, which prevented the diffusion of lanthanum. By immunoblot and immunofluorescence analysis, the expression and cellular localization of the tight junction and adherens-type junction proteins occludin, ZO-1, symplekin, beta-catenin, and plakoglobin were analyzed. ECV304 cells display further characteristics of endothelial cells, including the expresssion of thrombomodulin and of the vitronectin receptor CD51, as well as the secretion of plasminogen activator inhibitor 1 (PAI-1) and endothelin. However, ECV304 cells also express proteins characteristically found in epithelial cells, including E-cadherin and the desmosomal proteins desmoplakin, desmocollin, and desmoglein; occasionally desmosomal structures can be identified by electron microscopy. In conclusion, ECV304 cells express many endothelial markers and form specialized intercellular junctions that display some epithelial features. Thus this reportedly endothelial-derived permanent human cell line may be dedifferentiated toward an epithelial phenotype.
Subject(s)
Endothelium, Vascular/ultrastructure , Epithelial Cells/ultrastructure , Intercellular Junctions/physiology , Intercellular Junctions/ultrastructure , Nuclear Proteins , Trans-Activators , Animals , Cell Adhesion Molecules/analysis , Cell Communication , Cell Line , Cell Membrane/ultrastructure , Cytoskeletal Proteins/analysis , Desmocollins , Desmogleins , Desmoplakins , Dogs , Endothelium, Vascular/physiology , Epithelial Cells/physiology , Humans , Membrane Proteins/analysis , Microscopy, Electron , Occludin , Phosphoproteins/analysis , Proteins/analysis , Tight Junctions/ultrastructure , Umbilical Veins , Zonula Occludens-1 Protein , beta Catenin , gamma CateninABSTRACT
Human kidney proximal tubule epithelia express the ATP-dependent export pump for anionic conjugates encoded by the MRP2 (cMRP/cMOAT) gene (symbol ABCC2). MRP2, the apical isoform of the multidrug resistance protein, is an integral membrane glycoprotein with a molecular mass of approximately 190 kD that was originally cloned from liver and localized to the canalicular (apical) membrane domain of hepatocytes. In this study, MRP2 was detected in human kidney cortex by reverse transcription-PCR followed by sequencing of a 826-bp cDNA fragment and by immunoblotting using two different antibodies. Human MRP2 was localized to the apical brush-border membrane domain of proximal tubules by double and triple immunofluorescence microscopy including laser scanning microscopy. The expression of MRP2 in renal cell carcinoma was studied by reverse transcription-PCR and immunoblotting in samples from patients undergoing tumor-nephrectomy without prior chemotherapy. Clear-cell carcinomas, originating from the proximal tubule epithelium, expressed MRP2 in 95% (18 of 19) of cases. Immunofluorescence microscopy of MRP2 in clear-cell carcinoma showed a lack of a distinct apical-to-basolateral tumor cell polarity and an additional localization of MRP2 on intracellular membranes. MRP2, the first cloned ATP-dependent export pump for anionic conjugates detected in human kidney, may be involved in renal excretion of various anionic endogenous substances, xenobiotics, and cytotoxic drugs. This conjugate-transporting ATPase encoded by the MRP2 gene has a similar substrate specificity as the multidrug resistance protein MRP1, and may contribute to the multidrug resistance of renal clear-cell carcinomas.
Subject(s)
ATP Binding Cassette Transporter, Subfamily B/isolation & purification , Carcinoma, Renal Cell/genetics , Genes, MDR/genetics , Kidney Neoplasms/genetics , Kidney Tubules, Proximal/chemistry , Membrane Transport Proteins , Multidrug Resistance-Associated Proteins , ATP Binding Cassette Transporter, Subfamily B/genetics , Aged , Aged, 80 and over , Base Sequence , Carcinoma, Renal Cell/chemistry , Clone Cells , Dipeptidyl Peptidase 4/analysis , Gene Expression , Genetic Markers , Humans , Immunoblotting , Kidney Neoplasms/chemistry , Microscopy, Fluorescence , Middle Aged , Molecular Sequence Data , Multidrug Resistance-Associated Protein 2 , Polymerase Chain Reaction , RNA, Messenger/analysis , RNA, Neoplasm/analysis , Reference Values , Sensitivity and SpecificityABSTRACT
Administration of phalloidin, one of the toxic peptides of the mushroom Amanita phalloides, leads to rapid and sustained cholestasis in rats. Although attributed to the interaction of phalloidin with microfilaments, the events leading to cholestasis are incompletely understood. The adenosine triphosphate (ATP)-dependent, apical conjugate export pump, termed multidrug resistance protein 2 (Mrp2) or canalicular multispecific organic anion transporter, is the major driving force for bile salt-independent bile flow. We investigated the role of Mrp2 in phalloidin-induced cholestasis. Bile flow decreased to 53% and 31% of control at 15 and 30 minutes after phalloidin (0.5 mg/kg), respectively. Mrp2-mediated [3H]leukotriene excretion into bile during the initial 45 minutes was reduced to 44% of control when [3H]LTC4 was injected 15 minutes after phalloidin treatment. Mrp2 was progressively lost from the hepatocyte canalicular membrane and detected predominantly on intracellular membrane structures together with other canalicular proteins including P-glycoproteins, ecto-ATPase, and dipeptidyl-peptidase IV. By contrast, structures involved in intercellular adhesion (zonula occludens, zonula adhaerens, and desmosomes) as well as intermediate filaments of the cytokeratin type appeared largely unaffected within 30 minutes after phalloidin. In line with the immunofluorescence analysis, immunoblots indicated a loss of Mrp2 and P-glycoproteins from the canalicular membrane and a 3- and 4.6-fold increase of these transport proteins in the microsomal fraction, respectively. Our results indicate that phalloidin induces marked alterations of the hepatocyte canalicular architecture and a loss of Mrp2 together with other proteins from the canalicular membrane. The resulting cholestasis can therefore be explained in part by the loss of export pumps, including Mrp2, from the canalicular membrane.
Subject(s)
Carrier Proteins/metabolism , Cholestasis/chemically induced , Cholestasis/metabolism , Phalloidine , ATP Binding Cassette Transporter, Subfamily B/metabolism , Animals , Anion Transport Proteins , Bile/drug effects , Bile/metabolism , Bile/physiology , Female , Fluorescent Antibody Technique , Immunoblotting , Leukotrienes/metabolism , Liver/metabolism , Phalloidine/pharmacology , Rats , Rats, Wistar , Tissue DistributionABSTRACT
The human multidrug-resistance-associated protein (MRP), a member of the adenosine triphosphate (ATP)-binding cassette transporter superfamily, is frequently overexpressed in tumor cells resistant to antineoplastic drugs. In the rat, two Mrp isoforms have been identified, Mrp and cMrp. cMrp, also called Mrp2 or cMoat (canalicular multispecific organic anion transporter), is expressed in the canalicular membrane of rat hepatocytes and mediates the excretion of glucuronate, sulfate, and glutathione conjugates into bile. We investigated the expression of cMrp and Mrp in rat hepatocytes in primary culture. Treatment with the chemical carcinogen 2-acetylaminofluorene (2-AAF), the antineoplastic drug cisplatin, and the protein-synthesis inhibitor cycloheximide led to a dose-dependent and time-dependent increase in cmrp gene expression. A 347-base pair cmrp complementary DNA (cDNA) probe served to demonstrate the induction of cmrp messenger RNA (mRNA) with 40 micromol/L 2-AAF, 5 micromol/L cisplatin, or 5 micromol/L cycloheximide. An analogous response was obtained for the increase in cMrp protein. Mrp mRNA was below the detection limit in Northern blots of RNA from liver and hepatocyte cultures, in contrast to rat testis mRNA which served as a positive control. Immunofluorescence microscopy of cultured hepatocytes was used to visualize cMrp in the plasma membrane. Treatment with 2-AAF led to a marked increase in the immunofluorescence signal confirming the cMrp-inducing potency of 2-AAF. In conclusion, the inducing effect of the compounds studied may reflect a general inducibility of hepatic cMrp by a variety of cytotoxic, carcinogenic, and chemotherapeutic agents which is likely to be of relevance for the acquisition of multidrug resistance during chemotherapy and in the process of chemical carcinogenesis in the liver.
Subject(s)
2-Acetylaminofluorene/pharmacology , ATP-Binding Cassette Transporters/genetics , Carrier Proteins/genetics , Cisplatin/pharmacology , Cycloheximide/pharmacology , Gene Expression Regulation/drug effects , Liver/drug effects , Animals , Anion Transport Proteins , Cells, Cultured , Humans , Liver/cytology , Liver/metabolism , Male , Multidrug Resistance-Associated Proteins , Rats , Rats, WistarABSTRACT
A novel ATP-dependent export pump for amphiphilic anionic conjugates, which has been cloned recently from liver, was identified in rat kidney and localized to the apical membrane domain of proximal tubule epithelia. This 190-kD membrane glycoprotein (Mrp2) has been described previously as the hepatocyte canalicular isoform of the multidrug resistance protein and as the canalicular multispecific organic anion transporter. Mrp2 was identified in kidney by reverse transcription PCR followed by sequencing of the amplified 786-bp fragment and by immunoblotting, using an antibody specifically reacting with the carboxy terminus of rat Mrp2. Double immunofluorescence and confocal laser-scanning microscopy showed the presence of Mrp2 in the brush-border membrane domain of segments S1, S2, and S3 of proximal tubule epithelia. Mrp2 was not detectable in other segments of the nephron. The onset of Mrp2 expression during development occurred in a very early stage of nephron development. Mrp2 represents the first cloned ATP-dependent export pump for amphiphilic organic anions identified in kidney and localized to the apical membrane domain of proximal tubule epithelia. Mrp2 may contribute to cellular detoxification and to the secretion of endogenous and xenobiotic anionic substances, most of which are conjugates, from the blood into urine.
Subject(s)
Carrier Proteins/genetics , Kidney Tubules, Proximal/metabolism , Adenosine Triphosphate/metabolism , Animals , Anion Transport Proteins , Base Sequence , DNA Primers/genetics , Gene Expression , Immunoblotting , Ion Channels/genetics , Male , Membrane Glycoproteins/genetics , Microscopy, Confocal , Microscopy, Fluorescence , Polymerase Chain Reaction , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Rats, Mutant Strains , Rats, Sprague-DawleyABSTRACT
Simian virus 40 (SV40) has been shown to enter mammalian cells via uncoated plasma membrane invaginations. Viral particles subsequently appear within the endoplasmic reticulum. In the present study, we have examined the surface binding and internalization of SV40 by immunoelectron microscopy. We show that SV40 associates with surface pits which have the characteristics of caveolae and are labeled with antibodies to the caveolar marker protein, caveolin-1. SV40 is believed to use major histocompatibility complex (MHC) class I molecules as cell surface receptors. Using a number of MHC class I-specific monoclonal antibodies, we found that both viral infection and association of virus with caveolae were strongly reduced by preincubation with anti-MHC class I antibodies. Because binding of SV40 to MHC class I molecules may induce clustering, we investigated whether antibody cross-linked class I molecules also redistributed to caveolae. Clusters of MHC class I molecules were indeed shown to be specifically associated with caveolin-labeled surface pits. Taken together, the results suggest that SV40 may make use of MHC class I molecule clustering and the caveolae pathway to enter mammalian cells.
Subject(s)
Caveolins , Cell Membrane/virology , Histocompatibility Antigens Class I/metabolism , Organelles/virology , Simian virus 40/metabolism , Animals , Antibodies, Monoclonal/pharmacology , Antigens, Viral, Tumor/drug effects , Antigens, Viral, Tumor/metabolism , Caveolin 1 , Cells, Cultured , Membrane Proteins/metabolism , Mice , Organelles/metabolism , Simian virus 40/drug effectsABSTRACT
Human papillomaviruses (HPVs) are known to infect human keratinocytes and cause alterations in epithelial differentiation. We showed in this study that expression of the HPV-16 genome was able to interfere with the in vitro differentiation of a human simple-epithelial cell type, the 2102Ep teratocarcinoma cell line. Stable HPV-16 genome-expressing 2102Ep cell lines were generated, and subsequent alterations in differentiation were analyzed in comparison with parental 2102Ep cells. We found that in 2102Ep cells phorbol ester-induced differentiation led to changes in the expression of SSEA antigens, whereas in HPV-transfected cell lines only minor changes were observed.
Subject(s)
DNA, Viral/genetics , Papillomaviridae/genetics , Teratocarcinoma/pathology , Teratocarcinoma/virology , Testicular Neoplasms/pathology , Testicular Neoplasms/virology , Antigens, Neoplasm/biosynthesis , Antigens, Tumor-Associated, Carbohydrate , Cell Differentiation/drug effects , Cell Differentiation/physiology , Gene Expression , Genes, Viral , Glycosphingolipids/biosynthesis , Humans , Lewis X Antigen/biosynthesis , Male , Papillomaviridae/metabolism , Stage-Specific Embryonic Antigens , Teratocarcinoma/metabolism , Testicular Neoplasms/metabolism , Tetradecanoylphorbol Acetate/pharmacology , Transfection , Tumor Cells, CulturedABSTRACT
ATP-dependent transport of glutathione and glucuronate conjugates from hepatocytes into bile is mediated by a distinct member of the ATP-binding cassette superfamily. We have cloned and sequenced the canalicular isoform of the multidrug resistance protein from rat liver, and termed it cMrp. This membrane glycoprotein is composed of 1541 amino acids with an identity of 47.8% with the human multidrug resistance protein (MRP) and of 41.9% with the yeast cadmium factor (YCF1). The carboxyl-terminal 130 amino acids of the human hepatocyte canalicular isoform of MRP (cMRP) were 80.2% identical with rat cMrp. cMrp was not expressed in the liver of two mutant rat strains, the Eisai hyperbilirubinemic rat and the GY/TR- mutant, which are deficient in the ATP-dependent transport of conjugates across the canalicular membrane. Immunoblotting using an antibody raised against the carboxyl terminus of cMrp detected the glycoprotein of about 190 kDa only in the canalicular membrane from normal liver. Double immunofluorescence and confocal laser scanning microscopy localized cMrp exclusively to the canalicular membrane domain of hepatocytes and demonstrated its loss in the hyperbilirubinemic mutant rat. The results identify cMrp as a canalicular transport protein with a novel sequence and with a function similar to the one of the MRP.
Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/deficiency , ATP Binding Cassette Transporter, Subfamily B, Member 1/genetics , ATP-Binding Cassette Transporters , Bile Canaliculi/metabolism , Hyperbilirubinemia/metabolism , Liver/metabolism , Saccharomyces cerevisiae Proteins , ATP Binding Cassette Transporter, Subfamily B, Member 1/analysis , Adenosine Triphosphate/metabolism , Amino Acid Sequence , Animals , Cell Membrane/metabolism , Cloning, Molecular , Fluorescent Antibody Technique , Fungal Proteins/genetics , Humans , Hyperbilirubinemia/genetics , Leukotriene C4/metabolism , Molecular Sequence Data , Rats , Rats, Mutant Strains , Rats, Wistar , Saccharomyces cerevisiae/metabolism , Sequence Homology, Amino Acid , Transcription, GeneticABSTRACT
The Dubin-Johnson syndrome is characterized by an inherited defect in the secretion of amphiphilic anionic conjugates from hepatocytes into the bile. We have recently identified the membrane protein mediating the adenosine triphosphate (ATP)-dependent transport of glutathione and glucuronate conjugates as a multidrug-resistance protein (MRP) and localized it to the canalicular as well as to the lateral hepatocyte plasma membrane. In the present study we show the selective absence of the canalicular isoform of MRP (cMRP) from the hepatocytes in a patient with Dubin-Johnson syndrome by double-label immunofluorescence and confocal laser scanning microscopy using antibodies directed against MRP and dipeptidyl-peptidase IV (DPPIV). Another isoform of MRP was detected, however, in the lateral hepatocyte membrane of the patient. Moreover, MRP was present on immunoblots of erythrocyte membranes from Dubin-Johnson syndrome and normal humans. These findings are analogous to our recent observations on the localization of the rat homolog of MRP and its canalicular isoform, cMrp, in normal and transport-deficient GY/TR- Wistar rat liver. The elucidation of the selective absence of an isoform of MRP and from the canalicular membrane domain in conjunction with the defined substrate specificity of the MRP and cMRP gene-encoded conjugate export pumps contributes to the molecular definition of the transport defect in Dubin-Johnson syndrome.
Subject(s)
ATP-Binding Cassette Transporters/metabolism , Ion Pumps/metabolism , Isoenzymes/metabolism , Jaundice, Chronic Idiopathic/genetics , Liver/metabolism , Cell Membrane/enzymology , Cells, Cultured , Erythrocyte Membrane/enzymology , Female , Humans , Jaundice, Chronic Idiopathic/metabolism , Liver/cytology , Liver/enzymology , Microscopy, Confocal , Microscopy, Fluorescence , Middle Aged , Multidrug Resistance-Associated ProteinsABSTRACT
We have previously shown that the multi-drug resistance protein (MRP) mediates the ATP-dependent membrane transport of glutathione S-conjugates and additional amphiphilic organic anions. In the present study we demonstrate the expression of MRP in hepatocytes where it functions in hepatobiliary excretion. Analysis by reverse transcription-PCR of human and normal rat liver mRNA resulted in two expected cDNA fragments of MRP. Four different antibodies against MRP reacted on immunoblots with the glycoprotein of about 190 kD from human canalicular as well as basolateral hepatocyte membrane preparations. A polyclonal antibody directed against the carboxy-terminal sequence of MRP detected the rat homolog of MRP in liver. Double immunofluorescence microscopy and confocal laser scanning microscopy showed the presence of human MRP and rat Mrp in the canalicular as well as in the lateral membrane domains of hepatocytes. The transport function of the mrp gene-encoded conjugate export pump was assayed in plasma membrane vesicles with leukotriene C4 as a high-affinity glutathione S-conjugate substrate. The deficient ATP-dependent conjugate transport in canalicular membranes from TR- mutant rat hepatocytes was associated with a lack of amplification of one of the mrp cDNA fragments and with a selective loss of Mrp on immunoblots of canalicular membranes. Double immunofluorescence microscopy of livers from transport-deficient TR- mutant rats localized Mrp only to the lateral but not to the canalicular membrane. Our results indicate that the absence of Mrp or an isoform of Mrp from the canalicular membrane is the basis for the hereditary defect of the hepatobiliary excretion of anionic conjugates by the transport-deficient hepatocyte.
Subject(s)
ATP Binding Cassette Transporter, Subfamily B, Member 1/genetics , Bile Canaliculi/ultrastructure , Drug Resistance, Multiple/genetics , Liver/cytology , ATP Binding Cassette Transporter, Subfamily B, Member 1/analysis , ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism , Adenosine Triphosphate/physiology , Adult , Amino Acid Sequence , Animals , Anions/metabolism , Base Sequence , Bile Canaliculi/metabolism , Biological Transport/genetics , Blotting, Western , Cell Membrane/metabolism , DNA, Complementary/genetics , Fluorescent Antibody Technique , Gene Expression/physiology , Humans , Intracellular Membranes/metabolism , Leukotriene C4/metabolism , Liver/physiology , Liver/ultrastructure , Male , Microscopy, Confocal , Middle Aged , Molecular Sequence Data , Mutation/physiology , Polymerase Chain Reaction , RNA, Messenger/analysis , Rats , Rats, Wistar , TritiumABSTRACT
The human papillomavirus type 16 (HPV16) E5 protein is considered to have weak oncogenic properties, and its function in infected human keratinocytes is unknown. HPV16 E5 protein has been found to localize to the Golgi apparatus and the plasma membrane. To analyze the effect of E5 on plasma membrane properties, cells from the human keratinocyte cell line HaCaT were transfected with the HPV16 E5 open reading frame under the control of an inducible promoter. The gap junction-mediated cell-cell communication of E5- and vector-transfected cells was analyzed by microinjection of Lucifer yellow to measure dye coupling of the cells. A strong impairment of dye transfer in E5-transfected cells but not in vector-transfected cells was observed, with more than 80% dye transfer inhibition 40 min after injection. This impairment correlated with dephosphorylation of connexin 43, the major gap junctional protein in HaCaT cells. Furthermore, the dye coupling inhibition was not the result of differentiation of the E5-expressing cells, since no overexpression of cytokeratin 1 or filaggrin, markers of HaCaT cell differentiation, could be observed. These results therefore strongly suggest a correlation between expression of the HPV16 E5 open reading frame, impairment of gap junction-mediated dye coupling, and dephosphorylation of connexin 43.
Subject(s)
Cell Communication , Oncogene Proteins, Viral/physiology , Papillomaviridae/physiology , Cell Line , Connexin 43/genetics , Filaggrin Proteins , Humans , Keratinocytes/cytology , Oncogene Proteins, Viral/genetics , Open Reading Frames , PhosphorylationABSTRACT
We have shown previously using immunofluorescence microscopy that upon infection of polarized hippocampal cells in culture with vesicular stomatitis virus (VSV) and fowl plague virus (FPV) the VSV glycoprotein is delivered to the plasma membrane of the dendrites and of the cell body whereas the FPV hemagglutinin is transported to the axonal surface (Cell, 62 (1990) 63-72). In this work electron microscopy of infected rat hippocampal neurons showed that VSV progeny budded from the plasma membrane of the dendrites and the cell body. The location of the budding virions corresponded to the distribution of the VSV glycoprotein which was detected over the somatodendritic plasma membrane by immunoelectron microscopy. In contrast, no FPV formation was seen in the infected neurons although the FPV hemagglutinin was localized to the axonal surface by immunoelectron microscopy. In Semliki Forest virus (SFV) infected hippocampal cells we observed that the viral glycoproteins were exclusively present in the dendrites and cell body but not in axons.
Subject(s)
Cell Polarity/physiology , Hippocampus/microbiology , Membrane Glycoproteins/analysis , Neurons/microbiology , Viral Envelope Proteins/analysis , Animals , Cells, Cultured , Hippocampus/cytology , Influenza A virus/isolation & purification , Microscopy , Microscopy, Electron , Microscopy, Immunoelectron , Rats , Rats, Sprague-Dawley , Semliki forest virus/isolation & purification , Vesicular stomatitis Indiana virus/isolation & purificationABSTRACT
The release of intercellular contacts in MDBK cells, initiated by the depletion of Ca2+ ions from the culture medium, results in the endocytotic uptake of membrane vesicles containing specific membrane constituents of the zonula adhaerens (ZA). During this process the junction-derived, endocytosed vesicles remain associated with the ZA plaque components, while the plaque and its attached actin filaments retract as a whole in a ring-like fashion from the plasma membrane, often accumulating, usually in fragments, in the juxtanuclear cytoplasm. Double-label immunofluorescence microscopy with antiplakoglobin and antivinculin has indicated that both plaque proteins colocalize with the hallmark membrane glycoprotein of this junction type, E-cadherin (uvomorulin). When HRP used as a fluid phase marker is applied to the culture medium, simultaneously with the Ca2+ ion-chelator EGTA, numerous HRP-positive vesicles are found in close association with the dislocated plaque material, suggesting that the HRP is contained in the vesicles formed upon EGTA-induced junction splitting. Immunoelectron microscopy with various cadherin-specific antibodies revealed vesicle-associated labeling, confirming the derivation of these plaque-associated vesicles from the ZA. As the desmosome-specific cadherin, desmoglein, is recovered in another type of junction-derived vesicle, which is characterized by its association with a desmoplakin-plaque, we conclude that the membrane domains of both kinds of junction are endocytosed during Ca2+ depletion but stay in different vesicle populations, emphasizing the selective interaction of the specific cadherins with their respective plaque and filament partners.
Subject(s)
Cadherins/metabolism , Calcium/physiology , Intercellular Junctions/metabolism , Actins/metabolism , Animals , Cattle , Cell Adhesion , Cell Membrane/metabolism , Cells, Cultured , Desmosomes/metabolism , Desmosomes/ultrastructure , Endocytosis , Fluorescent Antibody Technique , Immunoenzyme Techniques , In Vitro Techniques , Intercellular Junctions/ultrastructure , Intracellular Membranes/metabolism , Kidney/cytology , Microscopy, ElectronABSTRACT
To examine whether constituent proteins of hemidesmosomal structures can be used as markers for certain pathways of epithelial differentiation we have examined the occurrence of the major M- approximately 230,000 plaque protein, the "bullous pemphigoid" (BP) antigen. Several bovine, rat and human tissues and bovine cell culture lines were examined, using different human autoantibody preparations in immunocytochemistry and immunoblotting. We report that this protein, also unequivocally identified by cDNA cloning from expression libraries and DNA sequencing, occurs not only in different stratified epithelia but also, apparently always in hemidesmosomal structures, in urothelium of bladder and the complex epithelia of trachea, bronchus and several glands, notably myoepithelium-containing skin glands, the mammary gland and salivary glands. The protein is absent, however, in all single-layered epithelia and in several tissues reported to have subplasmalemmal densities structurally similar to hemidesmosomes, such as Purkinje fibers of heart, meninges and perineuria. A mammary-gland-derived epithelial cell line (BMGE + H) is particularly rich in hemidesmosomes. This has been used to study the endocytotic uptake of hemidesmosome-containing plasma membrane domains into cytoplasmic vesicles upon detachment of cell sheets during treatment with dispase, a proteolytic enzyme. We propose to use the Mr- approximately 230,000 plaque protein as a marker selective for certain subsets of epithelial cell types and epithelium-derived tumors in studies of fetal and tumor development, including differentiation diagnosis of carcinomas.