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蛋白酪氨酸磷酸酶谱分析研究在小鼠原代棕色前体脂肪细胞棕色脂肪生成分化过程中的作用。

Protein tyrosine phosphatase profiling studies during brown adipogenic differentiation of mouse primary brown preadipocytes.

机构信息

Research Center for Integrated Cellulomics, KRIBB; Department of Functional Genomics, University of Science and Technology (UST), Daejeon 305-806, Korea

出版信息

BMB Rep. 2013 Nov;46(11):539-43. doi: 10.5483/bmbrep.2013.46.11.058.

Abstract

There is a correlation between obesity and the amount of brown adipose tissue; however, the molecular mechanism of brown adipogenic differentiation has not been as extensively studied. In this study, we performed a protein tyrosine phosphatase (PTP) profiling analysis during the brown adipogenic differentiation of mouse primary brown preadipocytes. Several PTPs, including PTPRF, PTPRZ, and DUSP12 showing differential expression patterns were identified. In the case of DUSP12, the expression level is dramatically downregulated during brown adipogenesis. The ectopic expression of DUSP12 using a retroviral expression system induces the suppression of adipogenic differentiation, whereas a catalytic inactive DUSP12 mutant showed no effect on differentiation. These results suggest that DUSP12 is involved in brown adipogenic differentiation and may be used as a target protein for the treatment or prevention of obesity by the regulation of brown adipogenic differentiation.

摘要

肥胖与棕色脂肪组织的含量之间存在相关性;然而,棕色脂肪形成分化的分子机制尚未得到广泛研究。在这项研究中,我们在小鼠原代棕色前体脂肪细胞的棕色脂肪形成分化过程中进行了蛋白质酪氨酸磷酸酶(PTP)谱分析。鉴定出了几种表现出差异表达模式的 PTP,包括 PTPRF、PTPRZ 和 DUSP12。在 DUSP12 的情况下,其表达水平在棕色脂肪形成过程中显著下调。使用逆转录病毒表达系统异位表达 DUSP12 可诱导脂肪生成分化受到抑制,而催化失活的 DUSP12 突变体对分化没有影响。这些结果表明 DUSP12 参与棕色脂肪形成分化,并且可以通过调节棕色脂肪形成分化作为治疗或预防肥胖的靶蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c2a/4133841/e9e5b224a5c7/BMB-46-539-g0001.jpg

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