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Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver

The high-density lipoprotein (HDL) receptor, scavenger receptor class B, type I (SR-BI), mediates selective cholesteryl ester uptake into the liver, which finally results in cholesterol secretion into the bile. Despite several reports, the distribution of hepatic SR-BI between the sinusoidal and can...

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Autores principales: Fruhwürth, Stefanie, Kovacs, Werner J., Bittman, Robert, Messner, Simon, Röhrl, Clemens, Stangl, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241236/
https://www.ncbi.nlm.nih.gov/pubmed/25059650
http://dx.doi.org/10.1007/s00418-014-1251-9
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author Fruhwürth, Stefanie
Kovacs, Werner J.
Bittman, Robert
Messner, Simon
Röhrl, Clemens
Stangl, Herbert
author_facet Fruhwürth, Stefanie
Kovacs, Werner J.
Bittman, Robert
Messner, Simon
Röhrl, Clemens
Stangl, Herbert
author_sort Fruhwürth, Stefanie
collection PubMed
description The high-density lipoprotein (HDL) receptor, scavenger receptor class B, type I (SR-BI), mediates selective cholesteryl ester uptake into the liver, which finally results in cholesterol secretion into the bile. Despite several reports, the distribution of hepatic SR-BI between the sinusoidal and canalicular membranes is still under debate. We present immunohistological data using specific markers showing that the bulk of SR-BI is present in sinusoidal membranes and, to a lesser extent, in canalicular membranes in murine and human liver sections. In addition, SR-BI was detected in preparations of rat liver canalicular membranes. We also compared the in vivo findings to HepG2 cells, a widely used in vitro hepatocyte model. Interestingly, SR-BI was enriched in bile canalicular-like (BC-like) structures in polarized HepG2 cells, which were cultivated either conventionally to form a monolayer or in Matrigel to form three-dimensional structures. Fluorescently labeled HDL was transported into close proximity of BC-like structures, whereas HDL labeled with the fluorescent cholesterol analog BODIPY-cholesterol was clearly detected within these structures. Importantly, similarly to human and mouse liver, SR-BI was localized in basolateral membranes in three-dimensional liver microtissues from primary human liver cells. Our results demonstrate that SR-BI is highly enriched in sinusoidal membranes and is also found in canalicular membranes. There was no significant basolateral–apical redistribution of hepatic SR-BI in fasting and refeeding experiments in mice. Furthermore, in vitro studies in polarized HepG2 cells showed explicit differences as SR-BI was highly enriched in BC-like structures. These structures are, however, functional and accumulated HDL-derived cholesterol. Thus, biological relevant model systems should be employed when investigating SR-BI distribution in vitro. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00418-014-1251-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-42412362014-11-25 Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver Fruhwürth, Stefanie Kovacs, Werner J. Bittman, Robert Messner, Simon Röhrl, Clemens Stangl, Herbert Histochem Cell Biol Original Paper The high-density lipoprotein (HDL) receptor, scavenger receptor class B, type I (SR-BI), mediates selective cholesteryl ester uptake into the liver, which finally results in cholesterol secretion into the bile. Despite several reports, the distribution of hepatic SR-BI between the sinusoidal and canalicular membranes is still under debate. We present immunohistological data using specific markers showing that the bulk of SR-BI is present in sinusoidal membranes and, to a lesser extent, in canalicular membranes in murine and human liver sections. In addition, SR-BI was detected in preparations of rat liver canalicular membranes. We also compared the in vivo findings to HepG2 cells, a widely used in vitro hepatocyte model. Interestingly, SR-BI was enriched in bile canalicular-like (BC-like) structures in polarized HepG2 cells, which were cultivated either conventionally to form a monolayer or in Matrigel to form three-dimensional structures. Fluorescently labeled HDL was transported into close proximity of BC-like structures, whereas HDL labeled with the fluorescent cholesterol analog BODIPY-cholesterol was clearly detected within these structures. Importantly, similarly to human and mouse liver, SR-BI was localized in basolateral membranes in three-dimensional liver microtissues from primary human liver cells. Our results demonstrate that SR-BI is highly enriched in sinusoidal membranes and is also found in canalicular membranes. There was no significant basolateral–apical redistribution of hepatic SR-BI in fasting and refeeding experiments in mice. Furthermore, in vitro studies in polarized HepG2 cells showed explicit differences as SR-BI was highly enriched in BC-like structures. These structures are, however, functional and accumulated HDL-derived cholesterol. Thus, biological relevant model systems should be employed when investigating SR-BI distribution in vitro. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00418-014-1251-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-07-25 2014 /pmc/articles/PMC4241236/ /pubmed/25059650 http://dx.doi.org/10.1007/s00418-014-1251-9 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Fruhwürth, Stefanie
Kovacs, Werner J.
Bittman, Robert
Messner, Simon
Röhrl, Clemens
Stangl, Herbert
Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver
title Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver
title_full Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver
title_fullStr Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver
title_full_unstemmed Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver
title_short Differential basolateral–apical distribution of scavenger receptor, class B, type I in cultured cells and the liver
title_sort differential basolateral–apical distribution of scavenger receptor, class b, type i in cultured cells and the liver
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241236/
https://www.ncbi.nlm.nih.gov/pubmed/25059650
http://dx.doi.org/10.1007/s00418-014-1251-9
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