Literature DB >> 18549352

Which in vitro models could be best used to study hepatocyte polarity?

Catherine Decaens1, Marjorie Durand, Brigitte Grosse, Doris Cassio.   

Abstract

The correct functioning of the liver is ensured by the setting and the maintenance of hepatocyte polarity. The complex polarity of the hepatocyte is characterized by the existence of several basolateral and apical poles per cell. Many in vitro models are available for studying hepatocyte polarity, but which are the more suitable? To answer this question, we aimed to identify criteria which determine the typical hepatocyte polarity. Therefore, we compiled a range of protein markers of membrane domains in rat hepatocytes and investigated their involvement in hepatocytic functions. Then, we focused on the relationship between hepatic functions and the cytoskeleton, Golgi apparatus and endoplasmic reticulum. Subsequently, we compared different cell lines expressing hepatocyte polarity. Finally, to demonstrate the usefulness of some of these lines, we presented new data on endoplasmic reticulum organization in relation to polarity.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18549352     DOI: 10.1042/BC20070127

Source DB:  PubMed          Journal:  Biol Cell        ISSN: 0248-4900            Impact factor:   4.458


  43 in total

1.  Regulatory subunit I-controlled protein kinase A activity is required for apical bile canalicular lumen development in hepatocytes.

Authors:  Kacper A Wojtal; Mandy Diskar; Friedrich W Herberg; Dick Hoekstra; Sven C D van Ijzendoorn
Journal:  J Biol Chem       Date:  2009-05-22       Impact factor: 5.157

Review 2.  Hepatocyte polarity.

Authors:  Aleksandr Treyer; Anne Müsch
Journal:  Compr Physiol       Date:  2013-01       Impact factor: 9.090

3.  AKAP350 Is involved in the development of apical "canalicular" structures in hepatic cells HepG2.

Authors:  Stella M Mattaloni; Elena Kolobova; Cristián Favre; Raúl A Marinelli; James R Goldenring; Maria C Larocca
Journal:  J Cell Physiol       Date:  2012-01       Impact factor: 6.384

4.  Microengineered cell and tissue systems for drug screening and toxicology applications: Evolution of in-vitro liver technologies.

Authors:  O B Usta; W J McCarty; S Bale; M Hegde; R Jindal; A Bhushan; I Golberg; M L Yarmush
Journal:  Technology (Singap World Sci)       Date:  2015-03

5.  Interplay among cellular polarization, lipoprotein metabolism and hepatitis C virus entry.

Authors:  Ignacio Benedicto; Francisca Molina-Jiménez; Ricardo Moreno-Otero; Manuel López-Cabrera; Pedro L Majano
Journal:  World J Gastroenterol       Date:  2011-06-14       Impact factor: 5.742

6.  Cytokinesis defines a spatial landmark for hepatocyte polarization and apical lumen formation.

Authors:  Ting Wang; Kilangsungla Yanger; Ben Z Stanger; Doris Cassio; Erfei Bi
Journal:  J Cell Sci       Date:  2014-04-04       Impact factor: 5.285

Review 7.  Blood-Bile Barrier: Morphology, Regulation, and Pathophysiology.

Authors:  Tirthadipa Pradhan-Sundd; Satdarshan Pal Monga
Journal:  Gene Expr       Date:  2019-01-15

8.  Claudin association with CD81 defines hepatitis C virus entry.

Authors:  Helen J Harris; Christopher Davis; Jonathan G L Mullins; Ke Hu; Margaret Goodall; Michelle J Farquhar; Christopher J Mee; Kitty McCaffrey; Stephen Young; Heidi Drummer; Peter Balfe; Jane A McKeating
Journal:  J Biol Chem       Date:  2010-04-07       Impact factor: 5.157

9.  Polarization restricts hepatitis C virus entry into HepG2 hepatoma cells.

Authors:  Christopher J Mee; Helen J Harris; Michelle J Farquhar; Garrick Wilson; Gary Reynolds; Christopher Davis; Sven C D van IJzendoorn; Peter Balfe; Jane A McKeating
Journal:  J Virol       Date:  2009-04-08       Impact factor: 5.103

10.  Three-dimensional Huh7 cell culture system for the study of Hepatitis C virus infection.

Authors:  Bruno Sainz; Veronica TenCate; Susan L Uprichard
Journal:  Virol J       Date:  2009-07-15       Impact factor: 4.099

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.