miR-146b/Btg2 axis as a potential inducer of islet beta-cell decline during the progression of obesity to T2DM
Weixuan Wang, Dan Ma, Yong Chen, Rui Cheng, Ting Zhang, Qian Ge, Xi Li

TL;DR
This study identifies miR-146b as a potential driver of beta-cell decline in the progression from obesity to type 2 diabetes.
Contribution
The novel finding is that miR-146b targets Btg2, contributing to beta-cell apoptosis and impaired insulin secretion.
Findings
miR-146b is upregulated in non-diabetic obesity and further in new-onset T2DM.
miR-146b overexpression increases beta-cell apoptosis and reduces insulin synthesis.
Btg2 overexpression reverses miR-146b-induced beta-cell dysfunction.
Abstract
We evaluated the potential mechanisms responsible for inducing beta-cell decline during the progression of obesity to type 2 diabetes mellitus (T2DM). Between February 2021 and February 2022, 25 subjects with non-diabetic obesity, 20 subjects with obesity and new-onset T2DM, and 25 healthy volunteers were recruited. Circulating exosome-contained miRNA expression profiling was performed by miRNA sequencing. The role of specific miRNA was analyzed by a gain-of-function approach in Min6 beta-cells, mouse islets, and human islets. Expression of 83 exosomal miRNAs was differently regulated in the circulation of subjects with non-diabetic obesity. We focused on miR-146b, which was mildly up-regulated in non-diabetic obesity and dramatically up-regulated in obese new-onset T2DM. Using an obese diabetic db/db mouse model, we found the expression of miR-146b to be mainly increased in islets.…
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Taxonomy
TopicsPancreatic function and diabetes · MicroRNA in disease regulation · RNA modifications and cancer
