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SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis

Mesenchymal stem cells have the capacity to give rise to multiple cell types, such as adipocytes, osteoblasts, chondrocytes, and myocytes. However, the molecular events responsible for the lineage specification and differentiation of mesenchymal stem cells remain unclear. Using gene expression profi...

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Autores principales: Lee, Hyemin, Lee, Yoo Jeong, Choi, Hyeonjin, Seok, Jo Woon, Yoon, Bo Kyung, Kim, Daeun, Han, Ji Yoon, Lee, Yoseob, Kim, Hyo Jung, Kim, Jae-woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665884/
https://www.ncbi.nlm.nih.gov/pubmed/29093466
http://dx.doi.org/10.1038/s41598-017-12512-2
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author Lee, Hyemin
Lee, Yoo Jeong
Choi, Hyeonjin
Seok, Jo Woon
Yoon, Bo Kyung
Kim, Daeun
Han, Ji Yoon
Lee, Yoseob
Kim, Hyo Jung
Kim, Jae-woo
author_facet Lee, Hyemin
Lee, Yoo Jeong
Choi, Hyeonjin
Seok, Jo Woon
Yoon, Bo Kyung
Kim, Daeun
Han, Ji Yoon
Lee, Yoseob
Kim, Hyo Jung
Kim, Jae-woo
author_sort Lee, Hyemin
collection PubMed
description Mesenchymal stem cells have the capacity to give rise to multiple cell types, such as adipocytes, osteoblasts, chondrocytes, and myocytes. However, the molecular events responsible for the lineage specification and differentiation of mesenchymal stem cells remain unclear. Using gene expression profile studies, we determined that Scavenger receptor class A, member 5 (SCARA5) is a novel mediator of adipocyte commitment. SCARA5 was expressed at a higher level in committed A33 preadipocyte cells compared to C3H10T1/2 pluripotent stem cells. Gain- and loss-of-function studies likewise revealed that SCARA5 acts as a mediator of adipocyte commitment and differentiation in both A33 and C3H10T1/2 cells. RNAi-mediated knockdown of SCARA5 in A33 cells markedly inhibited the adipogenic potential, whereas overexpression of SCARA5 enhanced adipocyte differentiation in C3H10T1/2 cells. We also demonstrated that the focal adhesion kinase (FAK) and ERK signaling pathways is associated with the SCARA5-mediated response, thereby modulating adipocyte lineage commitment and adipocyte differentiation. Additionally, glucocorticoids induced the expression of SCARA5 in differentiating adipocytes through glucocorticoids response elements (GRE) in the SCARA5 promoter. Taken together, our study demonstrates that SCARA5 is a positive regulator in adipocyte lineage commitment and early adipogenesis in mesenchymal stem cells.
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spelling pubmed-56658842017-11-08 SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis Lee, Hyemin Lee, Yoo Jeong Choi, Hyeonjin Seok, Jo Woon Yoon, Bo Kyung Kim, Daeun Han, Ji Yoon Lee, Yoseob Kim, Hyo Jung Kim, Jae-woo Sci Rep Article Mesenchymal stem cells have the capacity to give rise to multiple cell types, such as adipocytes, osteoblasts, chondrocytes, and myocytes. However, the molecular events responsible for the lineage specification and differentiation of mesenchymal stem cells remain unclear. Using gene expression profile studies, we determined that Scavenger receptor class A, member 5 (SCARA5) is a novel mediator of adipocyte commitment. SCARA5 was expressed at a higher level in committed A33 preadipocyte cells compared to C3H10T1/2 pluripotent stem cells. Gain- and loss-of-function studies likewise revealed that SCARA5 acts as a mediator of adipocyte commitment and differentiation in both A33 and C3H10T1/2 cells. RNAi-mediated knockdown of SCARA5 in A33 cells markedly inhibited the adipogenic potential, whereas overexpression of SCARA5 enhanced adipocyte differentiation in C3H10T1/2 cells. We also demonstrated that the focal adhesion kinase (FAK) and ERK signaling pathways is associated with the SCARA5-mediated response, thereby modulating adipocyte lineage commitment and adipocyte differentiation. Additionally, glucocorticoids induced the expression of SCARA5 in differentiating adipocytes through glucocorticoids response elements (GRE) in the SCARA5 promoter. Taken together, our study demonstrates that SCARA5 is a positive regulator in adipocyte lineage commitment and early adipogenesis in mesenchymal stem cells. Nature Publishing Group UK 2017-11-01 /pmc/articles/PMC5665884/ /pubmed/29093466 http://dx.doi.org/10.1038/s41598-017-12512-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Hyemin
Lee, Yoo Jeong
Choi, Hyeonjin
Seok, Jo Woon
Yoon, Bo Kyung
Kim, Daeun
Han, Ji Yoon
Lee, Yoseob
Kim, Hyo Jung
Kim, Jae-woo
SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
title SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
title_full SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
title_fullStr SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
title_full_unstemmed SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
title_short SCARA5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
title_sort scara5 plays a critical role in the commitment of mesenchymal stem cells to adipogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665884/
https://www.ncbi.nlm.nih.gov/pubmed/29093466
http://dx.doi.org/10.1038/s41598-017-12512-2
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