miR-876-3p regulates glucose homeostasis and insulin sensitivity by targeting adiponectin

Author:

Rajan Sujith12,Panzade Ganesh34,Srivastava Ankita12,Shankar Kripa1,Pandey Rajesh5,Kumar Durgesh12,Gupta Sanchita12,Gupta Abhishek1,Varshney Salil12,Beg Muheeb1,Mishra Raj Kumar6,Shankar Ravi34,Gaikwad Anil12

Affiliation:

1. 1Division of Pharmacology, CSIR-Central Drug Research Institute, Lucknow, India

2. 2Academy of Scientific and Innovative Research, CSIR-CDRI, Lucknow, India

3. 3Studio of Computational Biology and Bioinformatics, Biotechnology Division, CSIR-Institute of Himalayan Bioresource Technology, Palampur, India

4. 4Academy of Scientific and Innovative Research, CSIR-IHBT, Palampur, India

5. 5CSIR Ayurgenomics Unit-TRISUTRA, CSIR-Institute of Genomics and Integrative Biology, New Delhi, India

6. 6SIPS Superspeciality Hospital, Lucknow, India

Abstract

miRNA has been known to regulate diverse cellular and molecular functions. In the earlier study, we have reported that adipocytes differentiated from human mesenchymal stem cells (hMSC) on 72-h chronic insulin (CI) treatment exhibit insulin resistance (IR). Present study has further explored above model to investigate the role of early expressed miRNAs within human adipocytes to modulate differential adipokine expression as observed during IR. Our results highlight that miR-876-3p regulate glucose homeostasis and its dysregulation leads to IR. We found that miR-876-3p level is a critical determinant of adiponectin expression by virtue of its target within adiponectin 3′UTR. Regulatory effect of miR-876-3p impacts crosstalk between adiponectin and insulin signaling. Rosiglitazone treatment in CI-induced IR adipocytes drastically reduced miR-876-3p expression and increased adiponectin level. In line with this, lentiviral-mediated inhibition of miR-876-3p expression ameliorated CI and high-fat diet (HFD)-induced IR in adipocytes differentiated from hMSC and C57BL/6 mice, respectively. Our findings thus suggest that modulating miR-876-3p expression could provide novel opportunities for therapeutic intervention of obesity-associated metabolic syndrome.

Publisher

Bioscientifica

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference38 articles.

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