Suppr超能文献

磷蛋白磷酸酶1CB(PPP1CB)是一种新型的脂肪生成激活剂,可促进3T3-L1细胞的脂肪生成。

Phosphoprotein phosphatase 1CB (PPP1CB), a novel adipogenic activator, promotes 3T3-L1 adipogenesis.

作者信息

Cho Young-Lai, Min Jeong-Ki, Roh Kyung Min, Kim Won Kon, Han Baek Soo, Bae Kwang-Hee, Lee Sang Chul, Chung Sang J, Kang Hyo Jin

机构信息

Department of Chemistry, Dongguk University, Seoul 100-715, Republic of Korea.

Functional Genomics Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea; Department of Biomolecular Science, University of Science & Technology, Daejeon, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2015 Nov 13;467(2):211-7. doi: 10.1016/j.bbrc.2015.10.004. Epub 2015 Oct 9.

Abstract

Understanding the molecular networks that regulate adipogenesis is crucial for gaining insight into obesity and identifying medicinal targets thereof is necessary for pharmacological interventions. However, the identity and molecular actions of activators that promote the early development of adipocytes are still largely unknown. Here, we demonstrate a novel role for phosphoprotein phosphatase 1CB (PPP1CB) as a potent adipogenic activator that promotes adipocyte differentiation. PPP1CB expression increased in vitro during the early phase of 3T3-L1 adipogenesis and in the murine model of high-fat diet-induced obesity. Depletion of PPP1CB dramatically suppressed the differentiation of 3T3-L1 cells into mature adipocytes, with a concomitant change in adipocyte marker genes and significantly inhibited clonal expansion. We also showed that knockdown of PPP1CB caused a significant decrease in C/EBPδ expression, which in turn resulted in attenuation of PPARγ, C/EBPα, adiponectin, and aP2. In addition, we elucidated the functional significance of PPP1CB by linking p38 activation to C/EBPδ expression in early adipogenesis. Overall, our findings demonstrate a novel function of PPP1CB in promoting adipogenesis and suggest that PPP1CB may be a promising therapeutic target for treatment of obesity and obesity-related diseases.

摘要

了解调节脂肪生成的分子网络对于深入了解肥胖症至关重要,而确定其药物靶点对于药物干预是必要的。然而,促进脂肪细胞早期发育的激活剂的身份和分子作用仍 largely 未知。在这里,我们证明了磷酸蛋白磷酸酶 1CB(PPP1CB)作为一种有效的脂肪生成激活剂促进脂肪细胞分化的新作用。在 3T3-L1 脂肪生成的早期阶段以及高脂饮食诱导的肥胖小鼠模型中,PPP1CB 的表达在体外增加。PPP1CB 的缺失显著抑制了 3T3-L1 细胞向成熟脂肪细胞的分化,伴随着脂肪细胞标记基因的变化并显著抑制克隆扩增。我们还表明,PPP1CB 的敲低导致 C/EBPδ 表达显著降低,进而导致 PPARγ、C/EBPα、脂联素和 aP2 的减弱。此外,我们通过将 p38 激活与早期脂肪生成中的 C/EBPδ 表达联系起来阐明了 PPP1CB 的功能意义。总体而言,我们的发现证明了 PPP1CB 在促进脂肪生成中的新功能,并表明 PPP1CB 可能是治疗肥胖症和肥胖相关疾病的有前途的治疗靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验