spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Maurice, M.
Right arrow Articles by Feldmann, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Maurice, M.
Right arrow Articles by Feldmann, G.

Journal of Cell Science, Vol 90, Issue 1 79-92, Copyright © 1988 by Company of Biologists


JOURNAL ARTICLES

Formation of plasma membrane domains in rat hepatocytes and hepatoma cell lines in culture

M Maurice, E Rogier, D Cassio and G Feldmann
Institut National de la Sante et de la Recherche Medicale, Unite 24, Laboratoire de Biologie Cellulaire, Faculte de Medecine Xavier-Bichat, Paris, France.

In vivo, proteins of the hepatocyte plasma membrane are asymmetrically distributed, making it possible to distinguish a sinusoidal, a lateral and a canalicular domain. The conditions that determine hepatocyte plasma membrane polarity have been investigated in vitro, using three monoclonal antibodies directed against integral membrane proteins, which were characteristic of each domain. The localization of the three antigens was studied by immunolabelling of hepatocytes isolated from adult rat liver, primary monolayer cultures and rat hepatoma cell lines. When hepatocytes were isolated, the three antigens spread over the entire cell surface. The lateral antigen redistributed at lateral sites as soon as cell-cell contacts were established, 4 h after the beginning of primary culture. The sinusoidal and canalicular antigens became asymmetrically distributed after 48 h of primary culture, after the formation of bile canaliculus-like structures. In most of the hepatoma lines studied, the three antigens were expressed, except that the canalicular antigen was fully expressed in differentiated clones only. The lateral antigen was always distributed on the contiguous membranes of clustered hepatoma cells, whereas the sinusoidal and canalicular antigens were localized on the entire plasma membrane. However, in a few cells of some clones in which bile canaliculus-like structures were observed, the canalicular membranes were strongly labelled only with the canalicular antibody. In the absence of bile canalicular formations, in both primary culture and cell lines, the canalicular antigen and, to a lesser extent, the sinusoidal antigen accumulated in the Golgi apparatus, suggesting that their transport to the cell surface was altered in the absence of a bile pole. These results show that in hepatic cells, polarization of the plasma membrane is determined by: (1) the existence of cell-cell contacts, which is correlated with the domain-specific localization of the lateral antigen; and (2) the formation of bile canaliculi, which would trigger the development of an asymmetrical distribution of the sinusoidal and canalicular antigens.


This article has been cited by other articles:


Home page
J. Virol.Home page
A. Funk, H. Hohenberg, M. Mhamdi, H. Will, and H. Sirma
Spread of Hepatitis B Viruses In Vitro Requires Extracellular Progeny and May Be Codetermined by Polarized Egress
J. Virol., April 15, 2004; 78(8): 3977 - 3983.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
K. Ng, C Le Goascogne, E Amborade, B Stieger, and J Deschatrette
Reversible induction of rat hepatoma cell polarity with bile acids
J. Cell Sci., January 12, 2000; 113(23): 4241 - 4251.
[Abstract] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
X. Liu, E. L. LeCluyse, K. R. Brouwer, R. M. Lightfoot, J. I. Lee, and K. L. R. Brouwer
Use of Ca2+ Modulation to Evaluate Biliary Excretion in Sandwich-Cultured Rat Hepatocytes
J. Pharmacol. Exp. Ther., June 1, 1999; 289(3): 1592 - 1599.
[Abstract] [Full Text]


Home page
JCBHome page
C. Pous, K. Chabin, A. Drechou, L. Barbot, T. Phung-Koskas, C. Settegrana, M.L. Bourguet-Kondracki, M. Maurice, D. Cassio, M. Guyot, et al.
Functional Specialization of Stable and Dynamic Microtubules in Protein Traffic in WIF-B Cells
J. Cell Biol., July 13, 1998; 142(1): 153 - 165.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
V Bender, S Buschlen, and D Cassio
Expression and localization of hepatocyte domain-specific plasma membrane proteins in hepatoma x fibroblast hybrids and in hepatoma dedifferentiated variants
J. Cell Sci., January 11, 1998; 111(22): 3437 - 3450.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
I Hemery, A. Durand-Schneider, G Feldmann, J. Vaerman, and M Maurice
The transcytotic pathway of an apical plasma membrane protein (B10) in hepatocytes is similar to that of IgA and occurs via a tubular pericentriolar compartment
J. Cell Sci., January 6, 1996; 109(6): 1215 - 1227.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
C Decaens, P Rodriguez, C Bouchaud, and D Cassio
Establishment of hepatic cell polarity in the rat hepatoma-human fibroblast hybrid WIF-B9. A biphasic phenomenon going from a simple epithelial polarized phenotype to an hepatic polarized one
J. Cell Sci., January 6, 1996; 109(6): 1623 - 1635.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
M. Shanks, D Cassio, O Lecoq, and A. Hubbard
An improved polarized rat hepatoma hybrid cell line. Generation and comparison with its hepatoma relatives and hepatocytes in vivo
J. Cell Sci., January 4, 1994; 107(4): 813 - 825.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
G. Simonson, A. Vincent, K. Roberg, Y Huang, and V Iwanij
Molecular cloning and characterization of a novel liver-specific transport protein
J. Cell Sci., January 4, 1994; 107(4): 1065 - 1072.
[Abstract] [PDF]




© The Company of Biologists Ltd 1988