Cargando…

Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways

The formation of adipocytes during embryogenesis has been largely understudied. However, preadipocytes appear to originate from multipotent mesenchymal stromal/stem cells which migrate from the mesoderm to their anatomical localization. Most studies on adipocyte formation (adipogenesis) have used pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Ambele, Melvin A., Dhanraj, Priyanka, Giles, Rachel, Pepper, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349855/
https://www.ncbi.nlm.nih.gov/pubmed/32560163
http://dx.doi.org/10.3390/ijms21124283
_version_ 1783557151390695424
author Ambele, Melvin A.
Dhanraj, Priyanka
Giles, Rachel
Pepper, Michael S.
author_facet Ambele, Melvin A.
Dhanraj, Priyanka
Giles, Rachel
Pepper, Michael S.
author_sort Ambele, Melvin A.
collection PubMed
description The formation of adipocytes during embryogenesis has been largely understudied. However, preadipocytes appear to originate from multipotent mesenchymal stromal/stem cells which migrate from the mesoderm to their anatomical localization. Most studies on adipocyte formation (adipogenesis) have used preadipocytes derived from adult stem/stromal cells. Adipogenesis consists of two phases, namely commitment and terminal differentiation. This review discusses the role of signalling pathways, epigenetic modifiers, and transcription factors in preadipocyte commitment and differentiation into mature adipocytes, as well as limitations in our understanding of these processes. To date, a limited number of transcription factors, genes and signalling pathways have been described to regulate preadipocyte commitment. One reason could be that most studies on adipogenesis have used preadipocytes already committed to the adipogenic lineage, which are therefore not suitable for studying preadipocyte commitment. Conversely, over a dozen molecular players including transcription factors, genes, signalling pathways, epigenetic regulators, and microRNAs have been described to be involved in the differentiation of preadipocytes to adipocytes; however, only peroxisome proliferator-activated receptor gamma has proven to be clinically relevant. A detailed understanding of how the molecular players underpinning adipogenesis relate to adipose tissue function could provide new therapeutic approaches for addressing obesity without compromising adipose tissue function.
format Online
Article
Text
id pubmed-7349855
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-73498552020-07-15 Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways Ambele, Melvin A. Dhanraj, Priyanka Giles, Rachel Pepper, Michael S. Int J Mol Sci Review The formation of adipocytes during embryogenesis has been largely understudied. However, preadipocytes appear to originate from multipotent mesenchymal stromal/stem cells which migrate from the mesoderm to their anatomical localization. Most studies on adipocyte formation (adipogenesis) have used preadipocytes derived from adult stem/stromal cells. Adipogenesis consists of two phases, namely commitment and terminal differentiation. This review discusses the role of signalling pathways, epigenetic modifiers, and transcription factors in preadipocyte commitment and differentiation into mature adipocytes, as well as limitations in our understanding of these processes. To date, a limited number of transcription factors, genes and signalling pathways have been described to regulate preadipocyte commitment. One reason could be that most studies on adipogenesis have used preadipocytes already committed to the adipogenic lineage, which are therefore not suitable for studying preadipocyte commitment. Conversely, over a dozen molecular players including transcription factors, genes, signalling pathways, epigenetic regulators, and microRNAs have been described to be involved in the differentiation of preadipocytes to adipocytes; however, only peroxisome proliferator-activated receptor gamma has proven to be clinically relevant. A detailed understanding of how the molecular players underpinning adipogenesis relate to adipose tissue function could provide new therapeutic approaches for addressing obesity without compromising adipose tissue function. MDPI 2020-06-16 /pmc/articles/PMC7349855/ /pubmed/32560163 http://dx.doi.org/10.3390/ijms21124283 Text en © 2020 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
Ambele, Melvin A.
Dhanraj, Priyanka
Giles, Rachel
Pepper, Michael S.
Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways
title Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways
title_full Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways
title_fullStr Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways
title_full_unstemmed Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways
title_short Adipogenesis: A Complex Interplay of Multiple Molecular Determinants and Pathways
title_sort adipogenesis: a complex interplay of multiple molecular determinants and pathways
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349855/
https://www.ncbi.nlm.nih.gov/pubmed/32560163
http://dx.doi.org/10.3390/ijms21124283
work_keys_str_mv AT ambelemelvina adipogenesisacomplexinterplayofmultiplemoleculardeterminantsandpathways
AT dhanrajpriyanka adipogenesisacomplexinterplayofmultiplemoleculardeterminantsandpathways
AT gilesrachel adipogenesisacomplexinterplayofmultiplemoleculardeterminantsandpathways
AT peppermichaels adipogenesisacomplexinterplayofmultiplemoleculardeterminantsandpathways