Reproducibility of targeted gene expression measurements in human islets of Langerhans

被引:2
作者
Barry, R
Tadayyon, M
Green, IC [1 ]
机构
[1] Univ Sussex, Biochem Lab, Brighton BN1 9QG, E Sussex, England
[2] GlaxoSmithKline, Harlow CM19 5AW, Essex, England
[3] Univ Brighton, Brighton BN2 4GJ, E Sussex, England
关键词
human islets of Langerhans; targeted gene expression; glucotoxicity; insulin secretion; insulin synthesis; oxidative stress; radical scavenging; cell signalling; Fas/FasL; apoptosis;
D O I
10.1016/S0006-291X(02)02457-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The expression of 47 genes involved in the biosynthesis and secretion of insulin, apoptosis, and cellular stress was evaluated in isolated human islets using cDNA probes arrayed on, nitrocellulose membranes. Isolated human islets were cultured for four days, or one month, with glucose present at a concentration of either 5.5 or 16.7 mmol/L. Extracted islet total RNA was used to generate [P-32]dATP-labelled complex cDNA targets and hybridised with immobilised cDNA arrays. The positive expression of 45 mRNA transcripts in isolated human islets was documented. The coefficient of variance for relative levels of expression of transcripts was <25% for 9, 25-50% for 22, and 50-100% for 10, indicating good reproducibility between islet preparations from five different human pancreas donors. This study demonstrates the utility of nitrocellulose-based cDNA arrays for a focused reproducible analysis of gene expression changes in human islets of Langerhans. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:350 / 356
页数:7
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