PMID- 30015907 OWN - NLM STAT- MEDLINE DCOM- 20181108 LR - 20220121 IS - 1791-244X (Electronic) IS - 1107-3756 (Print) IS - 1107-3756 (Linking) VI - 42 IP - 4 DP - 2018 Oct TI - miR‑330‑5p inhibits H2O2‑induced adipogenic differentiation of MSCs by regulating RXRgamma. PG - 2042-2052 LID - 10.3892/ijmm.2018.3773 [doi] AB - The elucidation of the underlying molecular mechanism of H2O2‑induced adipocyte differentiation in mesenchymal stem cells (MSCs) is important for the development of treatments for metabolic diseases. The aim of the present study was to identify microRNA (miR)‑330‑5p, which targets retinoid X receptor gamma (RXRgamma) and to determine the function of H2O2‑induced adipogenic differentiation of MSCs. During differentiation of MSCs into adipocytes induced by H2O2, miR‑330‑5p expression was decreased with a concomitant increase in RXRgamma expression. A luciferase assay with RXRgamma 3'‑untranslated region (UTR) reporter plasmid, including the miR‑330‑5p‑binding sequences, identified that the introduction of miR‑330‑5p decreases luciferase activity. However, it did not affect the activity of mutated RXRgamma 3'‑UTR reporter. Enforced expression of miR‑330‑5p significantly inhibited adipocyte differentiation by decreasing RXRgamma mRNA and protein levels. In contrast, inhibition of the endogenous miR‑330‑5p promoted the formation of lipid droplets by rescuing RXRgamma expression. Furthermore, the effects of inhibition of RXRgamma were similar to those of overexpression of miR‑330‑5p on H2O2‑induced adipogenic differentiation from MSCs. miR‑330‑5p inhibits H2O2‑induced adipogenic differentiation of MSCs, and this is dependent on RXRgamma. Taken together, the results of the present study revealed that miR‑330‑5p acts as a critical regulator of RXRgamma, and is able to determinate the fate of MSCs to differentiate into adipocytes. This suggests that miR‑330‑5p and RXRgamma may be target molecules for controlling metabolic diseases. FAU - Huang, Weiping AU - Huang W AD - Research Center of Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. FAU - Li, Ke AU - Li K AD - Research Center of Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. FAU - Liu, Aijun AU - Liu A AD - Research Center of Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. FAU - Yang, Zeyu AU - Yang Z AD - Research Center of Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. FAU - Hu, Chenxia AU - Hu C AD - School of Pharmaceutical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. FAU - Chen, Dongfeng AU - Chen D AD - Research Center of Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. FAU - Wang, Hongqi AU - Wang H AD - Research Center of Integrative Medicine, School of Basic Medical Science, Guangzhou University of Chinese Medicine, Guangzhou, Guangdong 510006, P.R. China. LA - eng PT - Journal Article DEP - 20180712 PL - Greece TA - Int J Mol Med JT - International journal of molecular medicine JID - 9810955 RN - 0 (MIRN330 microRNA, rat) RN - 0 (MicroRNAs) RN - 0 (Retinoid X Receptor gamma) RN - BBX060AN9V (Hydrogen Peroxide) SB - IM MH - Adipogenesis/*drug effects MH - Animals MH - Cell Differentiation/*drug effects MH - Cells, Cultured MH - Gene Expression Regulation/*drug effects MH - Hydrogen Peroxide/*pharmacology MH - Mesenchymal Stem Cells/*metabolism MH - MicroRNAs/*metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Retinoid X Receptor gamma/*biosynthesis PMC - PMC6108853 EDAT- 2018/07/18 06:00 MHDA- 2018/11/09 06:00 PMCR- 2018/07/12 CRDT- 2018/07/18 06:00 PHST- 2018/02/06 00:00 [received] PHST- 2018/07/06 00:00 [accepted] PHST- 2018/07/18 06:00 [pubmed] PHST- 2018/11/09 06:00 [medline] PHST- 2018/07/18 06:00 [entrez] PHST- 2018/07/12 00:00 [pmc-release] AID - ijmm-42-04-2042 [pii] AID - 10.3892/ijmm.2018.3773 [doi] PST - ppublish SO - Int J Mol Med. 2018 Oct;42(4):2042-2052. doi: 10.3892/ijmm.2018.3773. Epub 2018 Jul 12.