Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3
Epithelium, a highly dynamic system, plays a key role in the homeostasis of the intestine. However, thus far a human intestinal epithelial cell line has not been established in many countries. Fetal tissue was selected to generate viable cell cultures for its sterile condition, effective generation,...
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Associação Brasileira de Divulgação Científica
2010-05-01
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doaj-4a45c3f826ff4c7f99bf34eb1ae298472020-11-24T20:58:10ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X2010-05-01435451459Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3Z. LiuP. ZhangY. ZhouH. QinT. ShenEpithelium, a highly dynamic system, plays a key role in the homeostasis of the intestine. However, thus far a human intestinal epithelial cell line has not been established in many countries. Fetal tissue was selected to generate viable cell cultures for its sterile condition, effective generation, and differentiated character. The purpose of the present study was to culture human intestinal epithelial cells by a relatively simple method. Thermolysin was added to improve the yield of epithelial cells, while endothelin-3 was added to stimulate their growth. By adding endothelin-3, the achievement ratio (viable cell cultures/total cultures) was enhanced to 60% of a total of 10 cultures (initiated from 8 distinct fetal small intestines), allowing the generation of viable epithelial cell cultures. Western blot, real-time PCR and immunofluorescent staining showed that cytokeratins 8, 18 and mouse intestinal mucosa-1/39 had high expression levels in human intestinal epithelial cells. Differentiated markers such as sucrase-isomaltase, aminopeptidase N and dipeptidylpeptidase IV also showed high expression levels in human intestinal epithelial cells. Differentiated human intestinal epithelial cells, with the expression of surface markers (cytokeratins 8, 18 and mouse intestinal mucosa-1/39) and secretion of cytokines (sucrase-isomaltase, aminopeptidase N and dipeptidylpeptidase IV), may be cultured by the thermolysin and endothelin-3 method and maintained for at least 20 passages. This is relatively simple, requiring no sophisticated techniques or instruments, and may have a number of varied applications.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2010000500006Human intestinal epithelial cellCell cultureThermolysinEndothelin-3CytokeratinBrush border enzyme |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Z. Liu P. Zhang Y. Zhou H. Qin T. Shen |
spellingShingle |
Z. Liu P. Zhang Y. Zhou H. Qin T. Shen Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 Brazilian Journal of Medical and Biological Research Human intestinal epithelial cell Cell culture Thermolysin Endothelin-3 Cytokeratin Brush border enzyme |
author_facet |
Z. Liu P. Zhang Y. Zhou H. Qin T. Shen |
author_sort |
Z. Liu |
title |
Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 |
title_short |
Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 |
title_full |
Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 |
title_fullStr |
Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 |
title_full_unstemmed |
Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 |
title_sort |
culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3 |
publisher |
Associação Brasileira de Divulgação Científica |
series |
Brazilian Journal of Medical and Biological Research |
issn |
0100-879X 1414-431X |
publishDate |
2010-05-01 |
description |
Epithelium, a highly dynamic system, plays a key role in the homeostasis of the intestine. However, thus far a human intestinal epithelial cell line has not been established in many countries. Fetal tissue was selected to generate viable cell cultures for its sterile condition, effective generation, and differentiated character. The purpose of the present study was to culture human intestinal epithelial cells by a relatively simple method. Thermolysin was added to improve the yield of epithelial cells, while endothelin-3 was added to stimulate their growth. By adding endothelin-3, the achievement ratio (viable cell cultures/total cultures) was enhanced to 60% of a total of 10 cultures (initiated from 8 distinct fetal small intestines), allowing the generation of viable epithelial cell cultures. Western blot, real-time PCR and immunofluorescent staining showed that cytokeratins 8, 18 and mouse intestinal mucosa-1/39 had high expression levels in human intestinal epithelial cells. Differentiated markers such as sucrase-isomaltase, aminopeptidase N and dipeptidylpeptidase IV also showed high expression levels in human intestinal epithelial cells. Differentiated human intestinal epithelial cells, with the expression of surface markers (cytokeratins 8, 18 and mouse intestinal mucosa-1/39) and secretion of cytokines (sucrase-isomaltase, aminopeptidase N and dipeptidylpeptidase IV), may be cultured by the thermolysin and endothelin-3 method and maintained for at least 20 passages. This is relatively simple, requiring no sophisticated techniques or instruments, and may have a number of varied applications. |
topic |
Human intestinal epithelial cell Cell culture Thermolysin Endothelin-3 Cytokeratin Brush border enzyme |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2010000500006 |
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