| Literature DB >> 11459924 |
H S Li1, J Y Zhang, B S Thompson, X Y Deng, M E Ford, P G Wood, D B Stolz, P K Eagon, D C Whitcomb.
Abstract
Individuals with chronic excessive alcohol ingestion are put at the risk of acute and chronic pancreatitis. Underlying molecular mechanisms are unknown. Differential gene expression in the pancreas was profiled using mRNA differential display by comparison between control and ethanol-consuming rats. Male Wistar rats were fed with diets containing 6.7% (vol/vol) ethanol for 4 wk. A cDNA tag that was overexpressed in the pancreas of rats fed ethanol was isolated. A 723-bp cDNA was cloned from a rat pancreatic cDNA library, which encodes a novel rat mitochondrial ATP synthase subunit 9, isoform 3 (ATP5G3), which is homologous to a human ATP5G3 gene. Real-time PCR demonstrated that all three nuclear gene isoforms (ATP5G1, ATP5G2, and ATP5G3) were consistently upregulated in the pancreas of alcohol-consuming rats, parallel with mitochondrial injury. The cellular response to mitochondrial damage and metabolic stress may reflect an adaptive process for mitochondrial repair in pancreatic acinar cells during chronic ethanol ingestion.Entities:
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Year: 2001 PMID： 11459924 DOI： 10.1152/physiolgenomics.2001.6.2.91
Source DB: PubMed Journal: Physiol Genomics ISSN： 1094-8341 Impact factor: 3.107