Formation of extensive canalicular networks by rat hepatocytes cultured in collagen-sandwich configuration
Abstract
Rat primary hepatocytes were cultured under different extracellular matrix configurations and evaluated for the acquisition and maintenance of structural and functional cell polarity. De novo repolarization of the plasma membrane was variable in rate and extent in hepatocyte cultures maintained on a conventional single layer of either gelled or ungelled collagen. However, cultures maintained in a collagen-sandwich configuration initiated uniform formation of a contiguous anastomosing network of bile canaliculi throughout the entire culture. Localization of apical membrane markers demonstrated normal distribution at the canalicular membrane. A marked rearrangement of the intracellular microfilaments to the cell periphery was observed and coincided with the development of the bile canaliculi. Acquisition of normal bile canalicular function and integrity was observed within 3-4 days postoverlay as indicated by the concentration and retention of carboxyfluorescein within the canalicular network. These results demonstrate that cultures of hepatocytes maintained in a sandwich configuration may serve as a more reliable and representative model in which to study the physiology of hepatic function as well as the morphogenesis of polarized membrane domains in vitro.
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LeCluyse et al. found that hepatocyte polarity was affected on single-layer gels; sandwich culture produced normal distribution of apical membrane markers at the canalicular membrane and well-established bile canaliculi.
“LeCluyse et al. (73) found that the polarity of hepatocytes was also affected when cultured on only single-layer gels.When a sandwich culture was used, a normal distribution of the apical membrane markers was found at the canalicular membrane, and bile canaliculi were also well established (73).”
From Modeling physiological events in 2D vs. 3D cell culture (2017) · cites this paper as [73]
Conventional 2D culture methods, flasks with or without ECM protein coatings, do not establish well enough the complex microenvironment that hepatocytes need to function.
“Hepatocytes in the liver are surrounded by a complex ECM, and several researchers have shown that conventional 2D culture methods, flasks with or without ECM protein coatings, do not establish well enough the complex microenvironment that hepatocytes need to function (29,34,73).”
From Modeling physiological events in 2D vs. 3D cell culture (2017) · cites this paper as [73]
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References 11 · Cited by 266
- Authors
- LeCluyse, E. L., Audus, K. L., & Hochman, J. H.
- Affiliations
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- Venue
- American Journal of Physiology-Cell Physiology
- Publisher
- American Physiological Society
- Published
- 1994-06-01
- Volume
- 266
- Issue
- 6
- Pages
- C1764-C1774
- ISSN
- 0363-6143 (ISSN-L)
- 1522-1563
- OpenAlex
- W2414945378
- Cited by
- 266
- References
- 11
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 4 · 2023: 3 · 2022: 9 · 2021: 7 · 2020: 5 · 2019: 9 · 2018: 11 · 2017: 6 · 2016: 12 · 2015: 11 · 2014: 15 · 2013: 13 · 2012: 21
- FWCI
- 4.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Physiology-Cell Physiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hepatology › Liver physiology and pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
- Keywords
- bile canaliculi, hepatocyte polarity, extracellular matrix, hepatocyte culture, rat hepatocytes
- MeSH terms
- Actins, Animals, Bile, Bile Canaliculi, Biological Transport, Cell Membrane, Cells, Cultured, Collagen, Cytological Techniques, Liver, Male, Actin Cytoskeleton, Biomarkers, Cell Polarity, Rats, Sprague-Dawley, Rats
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