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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Main Authors: Z. Liu, P. Zhang, Y. Zhou, H. Qin, T. Shen
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2010-05-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2010000500006
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spelling 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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