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MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3

MicroRNAs (miRNAs) influence stem cell functions, including mobilization, proliferation, and differentiation. miR-150 is abundantly expressed in monocytes. Knockdown of miR-150 promotes bone marrow stem cell migration. The role of miR-150 in adipose-derived stem cells (ADSCs) is unclear. In this stu...

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Autores principales: Li, Xiang, Zhao, Yu, Li, Xiuquan, Wang, Qiao, Ao, Qiang, Wang, Xiaohong, Tian, Xiaohong, Tong, Hao, Kong, Deyu, Chang, Shijie, Bai, Shuling, Fan, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875317/
https://www.ncbi.nlm.nih.gov/pubmed/31781236
http://dx.doi.org/10.1155/2019/2743047
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author Li, Xiang
Zhao, Yu
Li, Xiuquan
Wang, Qiao
Ao, Qiang
Wang, Xiaohong
Tian, Xiaohong
Tong, Hao
Kong, Deyu
Chang, Shijie
Bai, Shuling
Fan, Jun
author_facet Li, Xiang
Zhao, Yu
Li, Xiuquan
Wang, Qiao
Ao, Qiang
Wang, Xiaohong
Tian, Xiaohong
Tong, Hao
Kong, Deyu
Chang, Shijie
Bai, Shuling
Fan, Jun
author_sort Li, Xiang
collection PubMed
description MicroRNAs (miRNAs) influence stem cell functions, including mobilization, proliferation, and differentiation. miR-150 is abundantly expressed in monocytes. Knockdown of miR-150 promotes bone marrow stem cell migration. The role of miR-150 in adipose-derived stem cells (ADSCs) is unclear. In this study, the effects of miR-150 on adipogenic differentiation and proliferation of ADSCs were investigated. ADSCs were isolated from the inguinal adipose tissue of wild-type (WT) and miR-150 knockout (KO) mice and were induced for adipogenic differentiation. The miR-150 level was detected by real-time PCR. ADSCs were transfected by miR-150 or small-interfering RNA (siRNA) of Notch3. MTT assay and colony formation assay were performed in miR-150 knockdown and control ADSCs. Real-time PCR showed that miR-150 was expressed in ADSCs. miR-150 knockdown significantly decreased the capacity of adipogenic differentiation of ADSCs, as compared with their counterparts from WT mice. It is intriguing that the overexpression of miR-150 significantly increased C/EBPα and PPAR-γ expression and lipid formation in ADSCs with adipogenic induction. Overexpression of miR-150 significantly decreased Notch3 expression in ADSCs compared with the control groups. Furthermore, Notch3 inhibition promoted the adipogenic differentiation in ADSCs. miR-150 also suppressed proliferation potential and the expression of Nanog in ADSCs. In summary, this study demonstrates, for the first time, that miR-150 promotes adipogenic differentiation and inhibits proliferation of ADSCs. miR-150 regulates adipogenic differentiation of ADSCs, likely mediated by the downregulation of Notch3.
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spelling pubmed-68753172019-11-28 MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3 Li, Xiang Zhao, Yu Li, Xiuquan Wang, Qiao Ao, Qiang Wang, Xiaohong Tian, Xiaohong Tong, Hao Kong, Deyu Chang, Shijie Bai, Shuling Fan, Jun Stem Cells Int Research Article MicroRNAs (miRNAs) influence stem cell functions, including mobilization, proliferation, and differentiation. miR-150 is abundantly expressed in monocytes. Knockdown of miR-150 promotes bone marrow stem cell migration. The role of miR-150 in adipose-derived stem cells (ADSCs) is unclear. In this study, the effects of miR-150 on adipogenic differentiation and proliferation of ADSCs were investigated. ADSCs were isolated from the inguinal adipose tissue of wild-type (WT) and miR-150 knockout (KO) mice and were induced for adipogenic differentiation. The miR-150 level was detected by real-time PCR. ADSCs were transfected by miR-150 or small-interfering RNA (siRNA) of Notch3. MTT assay and colony formation assay were performed in miR-150 knockdown and control ADSCs. Real-time PCR showed that miR-150 was expressed in ADSCs. miR-150 knockdown significantly decreased the capacity of adipogenic differentiation of ADSCs, as compared with their counterparts from WT mice. It is intriguing that the overexpression of miR-150 significantly increased C/EBPα and PPAR-γ expression and lipid formation in ADSCs with adipogenic induction. Overexpression of miR-150 significantly decreased Notch3 expression in ADSCs compared with the control groups. Furthermore, Notch3 inhibition promoted the adipogenic differentiation in ADSCs. miR-150 also suppressed proliferation potential and the expression of Nanog in ADSCs. In summary, this study demonstrates, for the first time, that miR-150 promotes adipogenic differentiation and inhibits proliferation of ADSCs. miR-150 regulates adipogenic differentiation of ADSCs, likely mediated by the downregulation of Notch3. Hindawi 2019-10-30 /pmc/articles/PMC6875317/ /pubmed/31781236 http://dx.doi.org/10.1155/2019/2743047 Text en Copyright © 2019 Xiang Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Xiang
Zhao, Yu
Li, Xiuquan
Wang, Qiao
Ao, Qiang
Wang, Xiaohong
Tian, Xiaohong
Tong, Hao
Kong, Deyu
Chang, Shijie
Bai, Shuling
Fan, Jun
MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3
title MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3
title_full MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3
title_fullStr MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3
title_full_unstemmed MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3
title_short MicroRNA-150 Modulates Adipogenic Differentiation of Adipose-Derived Stem Cells by Targeting Notch3
title_sort microrna-150 modulates adipogenic differentiation of adipose-derived stem cells by targeting notch3
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875317/
https://www.ncbi.nlm.nih.gov/pubmed/31781236
http://dx.doi.org/10.1155/2019/2743047
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