Dual-specificity phosphatase 10 controls brown adipocyte differentiation by modulating the phosphorylation of p38 mitogen-activated protein kinase

Cited 24 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorHye-Ryung Choi-
dc.contributor.authorWon Kon-Kim-
dc.contributor.authorEun Young Kim-
dc.contributor.authorBaek Soo Han-
dc.contributor.authorJeong Ki Min-
dc.contributor.authorSeung-Wook Chi-
dc.contributor.authorSung Goo Park-
dc.contributor.authorKwang-Hee Bae-
dc.contributor.authorSang Chul Lee-
dc.date.accessioned2017-04-19T09:41:48Z-
dc.date.available2017-04-19T09:41:48Z-
dc.date.issued2013-
dc.identifier.issn1932-6203-
dc.identifier.uri10.1371/journal.pone.0072340ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11451-
dc.description.abstractBackground:Brown adipocytes play an important role in regulating the balance of energy, and as such, there is a strong correlation between obesity and the amount of brown adipose tissue. Although the molecular mechanism underlying white adipocyte differentiation has been well characterized, brown adipocyte differentiation has not been studied extensively. Here, we investigate the potential role of dual-specificity phosphatase 10 (DUSP10) in brown adipocyte differentiation using primary brown preadipocytes.Methods and Results:The expression of DUSP10 increased continuously after the brown adipocyte differentiation of mouse primary brown preadipocytes, whereas the phosphorylation of p38 was significantly upregulated at an early stage of differentiation followed by steep downregulation. The overexpression of DUSP10 induced a decrease in the level of p38 phosphorylation, resulting in lower lipid accumulation than that in cells overexpressing the inactive mutant DUSP10. The expression levels of several brown adipocyte markers such as PGC-1α, UCP1, and PRDM16 were also significantly reduced upon the ectopic expression of DUSP10. Furthermore, decreased mitochondrial DNA content was detected in cells expressing DUSP10. The results obtained upon treatment with the p38 inhibitor, SB203580, clearly indicated that the phosphorylation of p38 at an early stage is important in brown adipocyte differentiation. The effect of the p38 inhibitor was partially recovered by DUSP10 knockdown using RNAi.Conclusions:These results suggest that p38 phosphorylation is controlled by DUSP10 expression. Furthermore, p38 phosphorylation at an early stage is critical in brown adipocyte differentiation. Thus, the regulation of DUSP10 activity affects the efficiency of brown adipogenesis. Consequently, DUSP10 can be used as a novel target protein for the regulation of obesity.-
dc.publisherPublic Library of Science-
dc.titleDual-specificity phosphatase 10 controls brown adipocyte differentiation by modulating the phosphorylation of p38 mitogen-activated protein kinase-
dc.title.alternativeDual-specificity phosphatase 10 controls brown adipocyte differentiation by modulating the phosphorylation of p38 mitogen-activated protein kinase-
dc.typeArticle-
dc.citation.titlePLoS One-
dc.citation.number8-
dc.citation.endPagee72340-
dc.citation.startPagee72340-
dc.citation.volume8-
dc.contributor.affiliatedAuthorHye-Ryung Choi-
dc.contributor.affiliatedAuthorWon Kon-Kim-
dc.contributor.affiliatedAuthorEun Young Kim-
dc.contributor.affiliatedAuthorBaek Soo Han-
dc.contributor.affiliatedAuthorJeong Ki Min-
dc.contributor.affiliatedAuthorSeung-Wook Chi-
dc.contributor.affiliatedAuthorSung Goo Park-
dc.contributor.affiliatedAuthorKwang-Hee Bae-
dc.contributor.affiliatedAuthorSang Chul Lee-
dc.contributor.alternativeName최혜령-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName김은영-
dc.contributor.alternativeName한백수-
dc.contributor.alternativeName민정기-
dc.contributor.alternativeName지승욱-
dc.contributor.alternativeName박성구-
dc.contributor.alternativeName배광희-
dc.contributor.alternativeName이상철-
dc.identifier.bibliographicCitationPLoS One, vol. 8, no. 8, pp. e72340-e72340-
dc.identifier.doi10.1371/journal.pone.0072340-
dc.description.journalClassY-
Appears in Collections:
Division of Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Division of Research on National Challenges > Biodefense Research Center > 1. Journal Articles
Division of Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
Division of Biomedical Research > 1. Journal Articles
Division of Biomedical Research > Disease Target Structure Research Center > 1. Journal Articles
Files in This Item:

Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.