A technique for the culture of Barrett's oesophageal cells

ABSTRACT Establishment of cells in tissue culture from Barrett's columnar epithelium has been difficult. The aim of this study was to develop a successful tissue culture method employing a serumfree medium for cultivation of Barrett's epithelial cells. Fragments of Barrett's mucosal t...

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Veröffentlicht in:Journal of gastroenterology and hepatology 1997-08, Vol.12 (8), p.606-611
Hauptverfasser: KHAN, SEEMA M, PILLAY, S PRAGA, PAPADIMOS, DAVID, YONG, JOHN WK, ROBERTS, H JOHN V, CRAWFORD, DARRELL H
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container_end_page 611
container_issue 8
container_start_page 606
container_title Journal of gastroenterology and hepatology
container_volume 12
creator KHAN, SEEMA M
PILLAY, S PRAGA
PAPADIMOS, DAVID
YONG, JOHN WK
ROBERTS, H JOHN V
CRAWFORD, DARRELL H
description ABSTRACT Establishment of cells in tissue culture from Barrett's columnar epithelium has been difficult. The aim of this study was to develop a successful tissue culture method employing a serumfree medium for cultivation of Barrett's epithelial cells. Fragments of Barrett's mucosal tissue were explanted in a 3:1 mixture of Dulbecco's modification of Eagle's medium and Ham's F12, to initiate the outgrowth of epithelial cells. Subsequently, a commercial serum‐free medium (formulated for the growth of keratinocytes) was used for the propagation of Barrett's oesophagus cells without fibroblast growth. Cells established in culture retained their epithelial morphology, stained positive for cytokeratin, and contained Alcian blue (pH 2.5) and periodic acid‐Schiff reagent‐positive/diastase‐resistant vacuoles, confirming their origin from Barrett's epithelium. Electron microscopy showed tonofilaments, microvilli and desmosomes. Coating the surface of culture vessels was not required and four cell strains could be passaged up to 20 times with no fibroblast growth, in the keratinocyte serumfree medium.
doi_str_mv 10.1111/j.1440-1746.1997.tb00493.x
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The aim of this study was to develop a successful tissue culture method employing a serumfree medium for cultivation of Barrett's epithelial cells. Fragments of Barrett's mucosal tissue were explanted in a 3:1 mixture of Dulbecco's modification of Eagle's medium and Ham's F12, to initiate the outgrowth of epithelial cells. Subsequently, a commercial serum‐free medium (formulated for the growth of keratinocytes) was used for the propagation of Barrett's oesophagus cells without fibroblast growth. Cells established in culture retained their epithelial morphology, stained positive for cytokeratin, and contained Alcian blue (pH 2.5) and periodic acid‐Schiff reagent‐positive/diastase‐resistant vacuoles, confirming their origin from Barrett's epithelium. Electron microscopy showed tonofilaments, microvilli and desmosomes. 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Coating the surface of culture vessels was not required and four cell strains could be passaged up to 20 times with no fibroblast growth, in the keratinocyte serumfree medium.</description><subject>Barrett Esophagus - pathology</subject><subject>Biological and medical sciences</subject><subject>Cell Culture Techniques - methods</subject><subject>Culture Media</subject><subject>Epithelium - pathology</subject><subject>Epithelium - ultrastructure</subject><subject>Esophagus</subject><subject>Esophagus - pathology</subject><subject>Esophagus - ultrastructure</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Other diseases. 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Semiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KHAN, SEEMA M</creatorcontrib><creatorcontrib>PILLAY, S PRAGA</creatorcontrib><creatorcontrib>PAPADIMOS, DAVID</creatorcontrib><creatorcontrib>YONG, JOHN WK</creatorcontrib><creatorcontrib>ROBERTS, H JOHN V</creatorcontrib><creatorcontrib>CRAWFORD, DARRELL H</creatorcontrib><collection>Istex</collection><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>Journal of gastroenterology and hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KHAN, SEEMA M</au><au>PILLAY, S PRAGA</au><au>PAPADIMOS, DAVID</au><au>YONG, JOHN WK</au><au>ROBERTS, H JOHN V</au><au>CRAWFORD, DARRELL H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A technique for the culture of Barrett's oesophageal cells</atitle><jtitle>Journal of gastroenterology and hepatology</jtitle><addtitle>J Gastroenterol Hepatol</addtitle><date>1997-08</date><risdate>1997</risdate><volume>12</volume><issue>8</issue><spage>606</spage><epage>611</epage><pages>606-611</pages><issn>0815-9319</issn><eissn>1440-1746</eissn><abstract>ABSTRACT Establishment of cells in tissue culture from Barrett's columnar epithelium has been difficult. 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source MEDLINE; Access via Wiley Online Library
subjects Barrett Esophagus - pathology
Biological and medical sciences
Cell Culture Techniques - methods
Culture Media
Epithelium - pathology
Epithelium - ultrastructure
Esophagus
Esophagus - pathology
Esophagus - ultrastructure
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Medical sciences
Microscopy, Electron
Other diseases. Semiology
title A technique for the culture of Barrett's oesophageal cells
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