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Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis

The development, homeostasis, or increase of the adipose tissue is driven by the induction of the adipogenic differentiation (adipogenesis) of undifferentiated mesenchymal stem cells (MSCs). Adipogenesis can be inhibited by androgen stimulation of these MSCs resulting in the transcription initiation...

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Detalles Bibliográficos
Autores principales: Jansen, Julia, Greither, Thomas, Behre, Hermann M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6888160/
https://www.ncbi.nlm.nih.gov/pubmed/31744106
http://dx.doi.org/10.3390/ijms20225767
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author Jansen, Julia
Greither, Thomas
Behre, Hermann M.
author_facet Jansen, Julia
Greither, Thomas
Behre, Hermann M.
author_sort Jansen, Julia
collection PubMed
description The development, homeostasis, or increase of the adipose tissue is driven by the induction of the adipogenic differentiation (adipogenesis) of undifferentiated mesenchymal stem cells (MSCs). Adipogenesis can be inhibited by androgen stimulation of these MSCs resulting in the transcription initiation or repression of androgen receptor (AR) regulated genes. AR not only regulates the transcription of protein-coding genes but also the transcription of several non-coding microRNAs involved in the posttranscriptional gene regulation (herein designated as AndroMiRs). As microRNAs are largely involved in differentiation processes such as adipogenesis, the involvement of AndroMiRs in the androgen-mediated inhibition of adipogenesis is likely, however, not yet intensively studied. In this review, existing knowledge about adipogenesis-related microRNAs and AndroMiRs is summarized, and putative cross-links are drawn, which are still prone to experimental validation.
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spelling pubmed-68881602019-12-09 Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis Jansen, Julia Greither, Thomas Behre, Hermann M. Int J Mol Sci Review The development, homeostasis, or increase of the adipose tissue is driven by the induction of the adipogenic differentiation (adipogenesis) of undifferentiated mesenchymal stem cells (MSCs). Adipogenesis can be inhibited by androgen stimulation of these MSCs resulting in the transcription initiation or repression of androgen receptor (AR) regulated genes. AR not only regulates the transcription of protein-coding genes but also the transcription of several non-coding microRNAs involved in the posttranscriptional gene regulation (herein designated as AndroMiRs). As microRNAs are largely involved in differentiation processes such as adipogenesis, the involvement of AndroMiRs in the androgen-mediated inhibition of adipogenesis is likely, however, not yet intensively studied. In this review, existing knowledge about adipogenesis-related microRNAs and AndroMiRs is summarized, and putative cross-links are drawn, which are still prone to experimental validation. MDPI 2019-11-16 /pmc/articles/PMC6888160/ /pubmed/31744106 http://dx.doi.org/10.3390/ijms20225767 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jansen, Julia
Greither, Thomas
Behre, Hermann M.
Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis
title Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis
title_full Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis
title_fullStr Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis
title_full_unstemmed Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis
title_short Androgen-Regulated microRNAs (AndroMiRs) as Novel Players in Adipogenesis
title_sort androgen-regulated micrornas (andromirs) as novel players in adipogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6888160/
https://www.ncbi.nlm.nih.gov/pubmed/31744106
http://dx.doi.org/10.3390/ijms20225767
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