Effect of extracellular matrix topology on cell structure, function, and physiological responsiveness: hepatocytes cultured in a sandwich configuration
- PMID: 8940293
- DOI: 10.1096/fasebj.10.13.8940293
Effect of extracellular matrix topology on cell structure, function, and physiological responsiveness: hepatocytes cultured in a sandwich configuration
Abstract
Extracellular matrix (ECM) geometry is an important modulator of cell polarity and function. For example, 3-dimensional matrices often more effectively induce differentiated cell function than traditional 2-dimensional substrates. The effect of ECM topology can be investigated in a controlled fashion using a technique whereby cells cultured on a single surface are overlaid with a second layer of ECM, thereby creating a "sandwich" configuration. Confluent monolayers of epithelial or endothelial cells overlaid in this fashion often reorganize into structures that are reminiscent of their native tissue. In the case of hepatocytes, the overlay causes a dramatic reorganization of the cytoskeleton, adoption of in vivo-like morphology and polarity, and expression of a wide array of liver-specific functions. In this short review, we use the sandwiched hepatocyte culture system to illustrate the effect of ECM geometry on cellular function. Pertinent studies are summarized in the context of defining the parallels, strengths, and limitations of this culture system as an in vitro model to study the physiology and morphogenesis of liver tissue. We also explore some of its potential uses as a model to study liver pharmacology and toxicology, and for the development of liver preservation techniques and liver-assist devices.
Similar articles
-
Bile canaliculi formation and biliary transport in 3D sandwich-cultured hepatocytes in dependence of the extracellular matrix composition.Arch Toxicol. 2016 Oct;90(10):2497-511. doi: 10.1007/s00204-016-1758-z. Epub 2016 Jun 21. Arch Toxicol. 2016. PMID: 27325308
-
Three-dimensional culture of hepatocytes on porcine liver tissue-derived extracellular matrix.Biomaterials. 2011 Oct;32(29):7042-52. doi: 10.1016/j.biomaterials.2011.06.005. Epub 2011 Jul 1. Biomaterials. 2011. PMID: 21723601
-
Hepatocyte function and extracellular matrix geometry: long-term culture in a sandwich configuration.FASEB J. 1989 Feb;3(2):174-7. doi: 10.1096/fasebj.3.2.2914628. FASEB J. 1989. PMID: 2914628
-
Galactose-carrying polymers as extracellular matrices for liver tissue engineering.Biomaterials. 2006 Feb;27(4):576-85. doi: 10.1016/j.biomaterials.2005.06.008. Epub 2005 Aug 8. Biomaterials. 2006. PMID: 16084586 Review.
-
Sandwich-cultured hepatocytes: utility for in vitro exploration of hepatobiliary drug disposition and drug-induced hepatotoxicity.Expert Opin Drug Metab Toxicol. 2013 May;9(5):589-616. doi: 10.1517/17425255.2013.773973. Epub 2013 Mar 2. Expert Opin Drug Metab Toxicol. 2013. PMID: 23452081 Review.
Cited by
-
Encapsulation of Huh-7 cells within alginate-poly(ethylene glycol) hybrid microspheres.J Mater Sci Mater Med. 2012 Jan;23(1):171-9. doi: 10.1007/s10856-011-4512-3. Epub 2011 Dec 9. J Mater Sci Mater Med. 2012. PMID: 22160783
-
Bioengineered Cystinotic Kidney Tubules Recapitulate a Nephropathic Phenotype.Cells. 2022 Jan 5;11(1):177. doi: 10.3390/cells11010177. Cells. 2022. PMID: 35011739 Free PMC article.
-
Biodegradable meshes printed with extracellular matrix proteins support micropatterned hepatocyte cultures.Tissue Eng Part A. 2009 May;15(5):1169-79. doi: 10.1089/ten.tea.2008.0265. Tissue Eng Part A. 2009. PMID: 19072719 Free PMC article.
-
Type XII collagen regulates osteoblast polarity and communication during bone formation.J Cell Biol. 2011 Jun 13;193(6):1115-30. doi: 10.1083/jcb.201010010. J Cell Biol. 2011. PMID: 21670218 Free PMC article.
-
Hanging Drop, A Best Three-Dimensional (3D) Culture Method for Primary Buffalo and Sheep Hepatocytes.Sci Rep. 2017 Apr 26;7(1):1203. doi: 10.1038/s41598-017-01355-6. Sci Rep. 2017. PMID: 28446763 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources