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Calcium-Dependent Apoptotic Gene Expression in Cerulein-Treated AR42J Cells.

Authors :
YU, JI HOON
KIM, HYEYOUNG
KIM, KYUNG HWAN
Source :
Annals of the New York Academy of Sciences; 2004, Vol. 1010 Issue 1, p66-69, 4p
Publication Year :
2004

Abstract

Elevated Ca<superscript>2+</superscript> concentrations within the pancreatic acinar cells represent a risk factor for the development of acute pancreatitis. Apoptosis is an important characteristic of pancreatitis, with induction of apoptotic genes and intraceullar increase of calcium, endonucleases, and protease. The present study, which aims to investigate whether (1) cerulein induces apoptotic gene expression (bax, bid, p53) in pancreatic acinar AR42J cells and (2) cerulein-induced gene expression is mediated by intracellular Ca<superscript>2+</superscript>, monitored the gene expression profile in the cells treated with the Ca<superscript>2+</superscript> chelator BAPTA-AM. Results showed that cerulein (10<superscript>-7</superscript> M) evoked an initial peak Ca<superscript>2+</superscript> signal; a further Ca<superscript>2+</superscript> signal was induced with second treatment of cerulein. Cerulein-induced Ca<superscript>2+</superscript> signal could not be detected in the cells treated with the Ca<superscript>2+</superscript> chelator BAPTA-AM. Cerulein dose-dependently induced apoptosis, determined by DNA fragmentation and pro-apoptotic bid expression in AR42J cells. Cerulein induced bid, bax, and p53 mRNA expression, which was inhibited in the cells treated with cerulein and cultured in the presence of BAPTA-AM. The present results suggest that increase in the free cytosolic Ca<superscript>2+</superscript> may be the up- stream event of apoptotic gene (bax bid p53) expression, which contribute to cerulein-induced apoptosis in pancreatic acinar cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00778923
Volume :
1010
Issue :
1
Database :
Complementary Index
Journal :
Annals of the New York Academy of Sciences
Publication Type :
Academic Journal
Accession number :
26277482
Full Text :
https://doi.org/10.1196/annals.1299.009