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TRB3通过干扰Akt激活来调节C2C12分化。

TRB3 modulates C2C12 differentiation by interfering with Akt activation.

作者信息

Kato Satomi, Du Keyong

机构信息

The Molecular Oncology Research Institute, Tufts-New England Medical Center, 750 Washington St., Boston, MA 02111, USA.

出版信息

Biochem Biophys Res Commun. 2007 Feb 23;353(4):933-8. doi: 10.1016/j.bbrc.2006.12.161. Epub 2006 Dec 29.

Abstract

TRB3 is a member of TRB protein family characterized by containing a variant kinase domain without enzymatic activity. Interacting with Ser/Thr protein kinases Akt, TRB3 impairs Akt activation induced by growth factors and insulin. In this study we have examined the potential role of TRB3 in muscle differentiation. Our data indicated that the expression of TRB3 is downregulated during C2C12 cells undergoing muscle differentiation and that overexpression of TRB3 inhibits Akt activation during differentiation. Correspondingly, overexpression of TRB3 inhibits, while knockdown TRB3 enhances C2C12 differentiation. Thus, our studies indicated that TRB3 plays a critical role in muscle differentiation.

摘要

TRB3是TRB蛋白家族的成员,其特征是含有一个无酶活性的变异激酶结构域。TRB3与丝氨酸/苏氨酸蛋白激酶Akt相互作用,损害生长因子和胰岛素诱导的Akt激活。在本研究中,我们研究了TRB3在肌肉分化中的潜在作用。我们的数据表明,在C2C12细胞进行肌肉分化过程中,TRB3的表达下调,并且TRB3的过表达在分化过程中抑制Akt激活。相应地,TRB3的过表达抑制C2C12分化,而敲低TRB3则增强C2C12分化。因此,我们的研究表明TRB3在肌肉分化中起关键作用。

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