Literature DB >> 3792342

Studies on pancreatic acinar cells in tissue culture: basal lamina (basement membrane matrix promotes three-dimensional reorganization.

M Bendayan, M A Duhr, D Gingras.   

Abstract

Rat pancreatic acinar cells have been dissociated and maintained in culture under specific conditions which allow the retention of their differentiated state and three-dimensional organization. When cultured on a basal lamina (basement membrane) matrix, the cells first formed large monolayer patches and then reorganized themselves into acini-like structures. The cells regained their polarity around luminal spaces which appeared to be sealed off by well developed junctional complexes. Typical microvilli appeared at the "apical" plasma membrane projecting themselves into the luminal spaces. The intracellular organization resembled that of the cells in situ: a well developed rough endoplasmic reticulum located towards the "base" of the cell around a nucleus; a supranuclearly positioned Golgi apparatus and numerous secretory granules located in the "apical" region of the cell. Immunocytochemistry has revealed the presence of two pancreatic enzymes, amylase and chymotrypsinogen, in the various cellular compartments involved in secretion; the rough endoplasmic reticulum and Golgi cisternae as well as in the secretory granules. Biochemical evaluations have also shown the presence of amylase in the acinar cells and culture medium. These results thus demonstrate that dissociated pancreatic acinar cells maintained in culture under specific conditions reaggregate themselves into acini-like structures and retain their differentiated morphology as well as their ability to secrete.

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Year:  1986        PMID: 3792342

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  10 in total

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3.  The extracellular matrix coordinately modulates liver transcription factors and hepatocyte morphology.

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5.  Effects of substrata and method of tissue dissociation on adhesion, cytoskeleton, and growth of chick retinal pigmented epithelium in vitro.

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6.  Absence of trypsinogen autoactivation and immunolocalization of pancreatic secretory trypsin inhibitor in acinar cells in vitro.

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7.  Rat pancreatic interlobular duct epithelium: isolation and culture in collagen gel.

Authors:  S Githens; J A Schexnayder; K Desai; C L Patke
Journal:  In Vitro Cell Dev Biol       Date:  1989-08

8.  Primary culture of pancreatic (human) acinar cells.

Authors:  Lipi Singh; Dapinder K Bakshi; Rakesh Kumar Vasishta; Sunil Kumar Arora; Siddarth Majumdar; Jai Dev Wig
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9.  Mouse pancreatic acinar/ductular tissue gives rise to epithelial cultures that are morphologically, biochemically, and functionally indistinguishable from interlobular duct cell cultures.

Authors:  S Githens; J A Schexnayder; R L Moses; G M Denning; J J Smith; M L Frazier
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-09       Impact factor: 2.416

10.  In vitro secretion of zymogens by bovine pancreatic acini and ultra-structural analysis of exocytosis.

Authors:  Sivalingam Jayaveni; Kamaraj Nithyanandham; Chellan Rose
Journal:  Biochem Biophys Rep       Date:  2015-12-23
  10 in total

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