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Publication : Regulation of brown fat adipogenesis by protein tyrosine phosphatase 1B.

First Author  Matsuo K Year  2011
Journal  PLoS One Volume  6
Issue  1 Pages  e16446
PubMed ID  21305007 Mgi Jnum  J:169542
Mgi Id  MGI:4941263 Doi  10.1371/journal.pone.0016446
Citation  Matsuo K, et al. (2011) Regulation of brown fat adipogenesis by protein tyrosine phosphatase 1B. PLoS One 6(1):e16446
abstractText  BACKGROUND: Protein-tyrosine phosphatase 1B (PTP1B) is a physiological regulator of insulin signaling and energy balance, but its role in brown fat adipogenesis requires additional investigation. METHODOLOGY/PRINCIPAL FINDINGS: To precisely determine the role of PTP1B in adipogenesis, we established preadipocyte cell lines from wild type and PTP1B knockout (KO) mice. In addition, we reconstituted KO cells with wild type, substrate-trapping (D/A) and sumoylation-resistant (K/R) PTP1B mutants, then characterized differentiation and signaling in these cells. KO, D/A- and WT-reconstituted cells fully differentiated into mature adipocytes with KO and D/A cells exhibiting a trend for enhanced differentiation. In contrast, K/R cells exhibited marked attenuation in differentiation and lipid accumulation compared with WT cells. Expression of adipogenic markers PPARgamma, C/EBPalpha, C/EBPdelta, and PGC1alpha mirrored the differentiation pattern. In addition, the differentiation deficit in K/R cells could be reversed completely by the PPARgamma activator troglitazone. PTP1B deficiency enhanced insulin receptor (IR) and insulin receptor substrate 1 (IRS1) tyrosyl phosphorylation, while K/R cells exhibited attenuated insulin-induced IR and IRS1 phosphorylation and glucose uptake compared with WT cells. In addition, substrate-trapping studies revealed that IRS1 is a substrate for PTP1B in brown adipocytes. Moreover, KO, D/A and K/R cells exhibited elevated AMPK and ACC phosphorylation compared with WT cells. CONCLUSIONS: These data indicate that PTP1B is a modulator of brown fat adipogenesis and suggest that adipocyte differentiation requires regulated expression of PTP1B.
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