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Islet microRNAs in health and type-2 diabetes
被引:27
|作者:
Wendt, Anna
Esguerra, Jonathan L. S.
Eliasson, Lena
[1
]
机构:
[1] Lund Univ, Dept Clin Sci Malmo, Diabet Ctr, Islet Cell Exocytosis, Malmo, Sweden
基金:
瑞典研究理事会;
欧盟地平线“2020”;
关键词:
BETA-CELL FUNCTION;
INSULIN-SECRETION;
GLUCOSE;
EXPRESSION;
CLUSTER;
REGULATORS;
MIR-375;
GENES;
D O I:
10.1016/j.coph.2018.08.003
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Failure of the beta-cell to secrete enough insulin is a major contributing factor in the pathogenesis of type-2 diabetes (T2D). MicroRNAs provide an extra layer in the regulation of protein expression, and are thus involved in beta-cell compensation during development of the disease. In this review, we discuss how microRNAs can regulate their target protein expression and phenotypic output, present the status of nutritional regulation of microRNA expression, and summarize work on microRNA expression in human islets. In conclusion, current data lend support to microRNAs being essential regulators of insulin secretion. Future work will describe microRNAs in alpha-cell function, details of the microRNA mRNA network, and possibilities to use microRNAs as biomarkers and in therapeutic treatment of T2D and complications.
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页码:46 / 52
页数:7
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