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Enrichment and Characterization of Clonogenic Epithelial Cells from Adult Rat Liver and Initiation of Epithelial Cell Strains

A highly efficient method is described for obtaining proliferative epithelial cells from adult rat livers for the reproducible establishment of liver epithelial cell strains. When cells were isolated from livers of 10- to 15-wk-old male Fischer 344 rats by a collagenase-perfusion method, collected b...

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Published in:In Vitro Cellular & Developmental Biology 1987-05, Vol.23 (5), p.339-348
Main Authors: Kazunori Furukawa, Shimada, Tomiko, England, Patricia, Mochizuki, Yohichi, Williams, Gary M.
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Language:English
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cited_by cdi_FETCH-LOGICAL-c332t-d601d40fe8dc45ad6af4e1ea35291e40c986b841906932c042fea5a7e3fdf1633
cites cdi_FETCH-LOGICAL-c332t-d601d40fe8dc45ad6af4e1ea35291e40c986b841906932c042fea5a7e3fdf1633
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container_issue 5
container_start_page 339
container_title In Vitro Cellular & Developmental Biology
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creator Kazunori Furukawa
Shimada, Tomiko
England, Patricia
Mochizuki, Yohichi
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description A highly efficient method is described for obtaining proliferative epithelial cells from adult rat livers for the reproducible establishment of liver epithelial cell strains. When cells were isolated from livers of 10- to 15-wk-old male Fischer 344 rats by a collagenase-perfusion method, collected by centrifugation at 50 xg for 5 min, and cultured in Williams' medium E containing fetal bovine serum and dexamethasone, colonies of epithelial cells different in size and morphology from hepatocytes were obtained. Sequential perfusion with collagenase and dispase yielded numerous epithelial cell colonies. When isolated cells were fractionated by differential centrifugation, the great majority of hepatocytes were sedimented at 50 xg for 1 min, whereas many non-hepatocytic cells remained in the supernatant and could be sedimented by a second centrifugation at 50 xg for 5 min. Culture of the two fractions revealed that almost all the epithelial cell colonies were derived from cells in the non-hepatocytic cell fraction. The epithelial cells were cytochemically negative for γ-glutamyl transpeptidase activity, whereas an increase in the activity was detected in hepatocytes with duration in culture. Ultrastructural characteristics of hepatocytes were not found in the cells of newly established cell strains. These results suggest that adult rat liver epithelial cells propagable in culture were derived from a cell type other than the hepatocyte.
doi_str_mv 10.1007/BF02620990
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When cells were isolated from livers of 10- to 15-wk-old male Fischer 344 rats by a collagenase-perfusion method, collected by centrifugation at 50 xg for 5 min, and cultured in Williams' medium E containing fetal bovine serum and dexamethasone, colonies of epithelial cells different in size and morphology from hepatocytes were obtained. Sequential perfusion with collagenase and dispase yielded numerous epithelial cell colonies. When isolated cells were fractionated by differential centrifugation, the great majority of hepatocytes were sedimented at 50 xg for 1 min, whereas many non-hepatocytic cells remained in the supernatant and could be sedimented by a second centrifugation at 50 xg for 5 min. Culture of the two fractions revealed that almost all the epithelial cell colonies were derived from cells in the non-hepatocytic cell fraction. The epithelial cells were cytochemically negative for γ-glutamyl transpeptidase activity, whereas an increase in the activity was detected in hepatocytes with duration in culture. Ultrastructural characteristics of hepatocytes were not found in the cells of newly established cell strains. These results suggest that adult rat liver epithelial cells propagable in culture were derived from a cell type other than the hepatocyte.</description><subject>Animal cells</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell cultures. Hybridization. Fusion</subject><subject>Cell Division</subject><subject>Cell Fractionation</subject><subject>Cell growth</subject><subject>Cell lines</subject><subject>Cells, Cultured</subject><subject>Centrifugation</subject><subject>Cultured cells</subject><subject>Endothelial cells</subject><subject>Epithelial Cells</subject><subject>Establishment of new cell lines, improvement of cultural methods, mass cultures</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hepatocytes</subject><subject>Histocytochemistry</subject><subject>Liver</subject><subject>Liver - cytology</subject><subject>Liver cells</subject><subject>Male</subject><subject>Methods. Procedures. 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Hybridization. Fusion</topic><topic>Cell Division</topic><topic>Cell Fractionation</topic><topic>Cell growth</topic><topic>Cell lines</topic><topic>Cells, Cultured</topic><topic>Centrifugation</topic><topic>Cultured cells</topic><topic>Endothelial cells</topic><topic>Epithelial Cells</topic><topic>Establishment of new cell lines, improvement of cultural methods, mass cultures</topic><topic>Eukaryotic cell cultures</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hepatocytes</topic><topic>Histocytochemistry</topic><topic>Liver</topic><topic>Liver - cytology</topic><topic>Liver cells</topic><topic>Male</topic><topic>Methods. Procedures. Technologies</topic><topic>Microscopy, Phase-Contrast</topic><topic>Molecular and cellular biology</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Seeding</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kazunori Furukawa</creatorcontrib><creatorcontrib>Shimada, Tomiko</creatorcontrib><creatorcontrib>England, Patricia</creatorcontrib><creatorcontrib>Mochizuki, Yohichi</creatorcontrib><creatorcontrib>Williams, Gary M.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>In Vitro Cellular &amp; Developmental Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kazunori Furukawa</au><au>Shimada, Tomiko</au><au>England, Patricia</au><au>Mochizuki, Yohichi</au><au>Williams, Gary M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enrichment and Characterization of Clonogenic Epithelial Cells from Adult Rat Liver and Initiation of Epithelial Cell Strains</atitle><jtitle>In Vitro Cellular &amp; Developmental Biology</jtitle><addtitle>In Vitro Cell Dev Biol</addtitle><date>1987-05-01</date><risdate>1987</risdate><volume>23</volume><issue>5</issue><spage>339</spage><epage>348</epage><pages>339-348</pages><issn>0883-8364</issn><eissn>2327-431X</eissn><eissn>1475-2689</eissn><coden>ICDBEO</coden><abstract>A highly efficient method is described for obtaining proliferative epithelial cells from adult rat livers for the reproducible establishment of liver epithelial cell strains. When cells were isolated from livers of 10- to 15-wk-old male Fischer 344 rats by a collagenase-perfusion method, collected by centrifugation at 50 xg for 5 min, and cultured in Williams' medium E containing fetal bovine serum and dexamethasone, colonies of epithelial cells different in size and morphology from hepatocytes were obtained. Sequential perfusion with collagenase and dispase yielded numerous epithelial cell colonies. When isolated cells were fractionated by differential centrifugation, the great majority of hepatocytes were sedimented at 50 xg for 1 min, whereas many non-hepatocytic cells remained in the supernatant and could be sedimented by a second centrifugation at 50 xg for 5 min. Culture of the two fractions revealed that almost all the epithelial cell colonies were derived from cells in the non-hepatocytic cell fraction. The epithelial cells were cytochemically negative for γ-glutamyl transpeptidase activity, whereas an increase in the activity was detected in hepatocytes with duration in culture. Ultrastructural characteristics of hepatocytes were not found in the cells of newly established cell strains. These results suggest that adult rat liver epithelial cells propagable in culture were derived from a cell type other than the hepatocyte.</abstract><cop>Largo, MD</cop><pub>Tissue Culture Association, Inc</pub><pmid>3294781</pmid><doi>10.1007/BF02620990</doi><tpages>10</tpages></addata></record>
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identifier ISSN: 0883-8364
ispartof In Vitro Cellular & Developmental Biology, 1987-05, Vol.23 (5), p.339-348
issn 0883-8364
2327-431X
1475-2689
language eng
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source JSTOR Archival Journals and Primary Sources Collection; Springer LINK Archives
subjects Animal cells
Animals
Biological and medical sciences
Biotechnology
Cell cultures. Hybridization. Fusion
Cell Division
Cell Fractionation
Cell growth
Cell lines
Cells, Cultured
Centrifugation
Cultured cells
Endothelial cells
Epithelial Cells
Establishment of new cell lines, improvement of cultural methods, mass cultures
Eukaryotic cell cultures
Fundamental and applied biological sciences. Psychology
Hepatocytes
Histocytochemistry
Liver
Liver - cytology
Liver cells
Male
Methods. Procedures. Technologies
Microscopy, Phase-Contrast
Molecular and cellular biology
Rats
Rats, Inbred F344
Seeding
title Enrichment and Characterization of Clonogenic Epithelial Cells from Adult Rat Liver and Initiation of Epithelial Cell Strains
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