Differences in islet-enriched miRNAs in healthy and glucose intolerant human subjects

被引:80
作者
Bolmeson, Caroline [1 ]
Esguerra, Jonathan L. S.
Salehi, Albert [2 ]
Speidel, Dina
Eliasson, Lena
Cilio, Corrado M. [1 ]
机构
[1] Lund Univ, Malmo Univ Hosp, Dept Clin Sci Malmo, Cellular Autoimmun Unit, S-20502 Malmo, Sweden
[2] Lund Univ, Malmo Univ Hosp, Dept Clin Sci Malmo, Ctr Diabet, S-20502 Malmo, Sweden
基金
瑞典研究理事会;
关键词
Human; Pancreatic islet; beta-Cell; miRNA; Insulin secretion; Diabetes; PANCREATIC BETA-CELLS; GENOME-WIDE ASSOCIATION; GENETIC-VARIATION; INSULIN; MICRORNAS; EXPRESSION; INVOLVEMENT; BIOGENESIS; PATHWAYS; TARGETS;
D O I
10.1016/j.bbrc.2010.11.024
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
Many microRNAs (miRNAs) are known to be cell-type specific and are implicated in development of diseases. We investigated the global expression pattern of miRNAs in human pancreatic islets compared to liver and skeletal muscle, using bead-based technology and quantitative RT-PCR. In addition to the known islet-specific miR-375, we also found enrichment of miR-127-3p, miR-184, miR-195 and miR-493* in the pancreatic islets. The expression of miR-375, miR-127-3p, miR-184 and the liver-enriched miR-122 is positively correlated to insulin biosynthesis, while the expression of miR-127-3p and miR-184 is negatively correlated to glucose-stimulated insulin secretion (GSIS). These correlations were absent in islets of glucose intolerant donors (HbAlc >= 6.1). We suggest that the presence of an islet-specific miRNA network, which consists of at least miR-375, miR-127-3p and miR-184, potentially involved in insulin secretion. Our results provide new insight into miRNA-mediated regulation of insulin secretion in healthy and glucose intolerant subjects. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 22
页数:7
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