Hornberger Troy Alan, Sukhija Kunal Balu, Wang Xiao-Rong, Chien Shu
Department of Bioengineering, University of California San Diego, 9500 Gilman Drive., La Jolla, CA 92093-0412, USA.
FEBS Lett. 2007 Oct 2;581(24):4562-6. doi: 10.1016/j.febslet.2007.08.045. Epub 2007 Aug 31.
Mechanical stretch induces phosphorylation of the hydrophobic motif site Thr(389) in p70(S6k) through a rapamycin-sensitive (RS) pathway that involves a unique PI3K-independent mechanism. Rapamycin is considered to be a highly specific inhibitor of the protein kinase mTOR; however, mTOR is also considered to be a PI3K-dependent signaling molecule. Thus, questions remain as to whether mTOR is the RS element that confers mechanically-induced signaling to p70(S6k)(389). In this study, rapamycin-resistant mutants of mTOR along with mechanical stretch were used to address this question. The results indicate that mTOR is the RS element and reveal that mTOR signaling can be activated through a PI3K-independent mechanism.
机械牵张通过一种对雷帕霉素敏感(RS)的途径诱导p70核糖体蛋白S6激酶(p70(S6k))中疏水基序位点苏氨酸(Thr(389))的磷酸化,该途径涉及一种独特的不依赖磷脂酰肌醇-3激酶(PI3K)的机制。雷帕霉素被认为是蛋白激酶哺乳动物雷帕霉素靶蛋白(mTOR)的一种高度特异性抑制剂;然而,mTOR也被认为是一种依赖PI3K的信号分子。因此,关于mTOR是否是赋予p70(S6k)(389)机械诱导信号的RS元件仍存在疑问。在本研究中,使用mTOR的雷帕霉素抗性突变体以及机械牵张来解决这个问题。结果表明mTOR是RS元件,并揭示mTOR信号传导可通过不依赖PI3K的机制被激活。