Microenvironmental regulation of the sinusoidal endothelial cell phenotype in vitro
Author(s)
March, Sandra; Hui, Elliot E.; Underhill, Gregory; Khetani, Salman R.; Bhatia, Sangeeta N.
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Liver sinusoidal endothelial cells (LSECs) differ, both structurally and functionally, from endothelial cells (ECs) lining blood vessels of other tissues. For example, in contrast to other ECs, LSECs possess fenestrations, have low detectable levels of platelet endothelial cell adhesion molecule 1 expression, and in rat tissue, they distinctively express a cell surface marker recognized by the SE-1 antibody. These unique phenotypic characteristics seen in hepatic tissue are lost over time upon culture in vitro; therefore, this study sought to systematically examine the effects of microenvironmental stimuli—namely, extracellular matrix and neighboring cells, on the LSEC phenotype in vitro. In probing the role of the underlying extracellular matrix, we identified collagen I and collagen III as well as mixtures of collagen I/collagen IV/fibronectin as having a positive effect on LSEC survival. Furthermore, using a stable hepatocellular model (hepatocyte–fibroblast) we were able to prolong the expression of both SE-1 and phenotypic functions of LSEC such as factor VIII activity and AcLOL uptake in cocultured LSECs through the production of short-range paracrine signals. In the course of these experiments, we identified the antigen recognized by SE-1 as CD32b. Conclusion: Collectively, this study has identified several microenvironmental regulators of liver sinusoidal endothelial cells that prolong their phenotypic functions for up to 2 weeks in culture, enabling the development of better in vitro models of liver physiology and disease.
Description
Author Manuscript: 2010 June 23.
Date issued
2009-05Department
move to dc.description.sponsorship; Harvard University--MIT Division of Health Sciences and TechnologyJournal
Hepatology
Publisher
Wiley Blackwell
Citation
March, Sandra et al. “Microenvironmental Regulation of the Sinusoidal Endothelial Cell Phenotype in Vitro.” Hepatology 50.3 (2009): 920–928. Copyright © 2009 American Association for the Study of Liver Diseases
Version: Author's final manuscript
ISSN
0270-9139
1527-3350