Department of Biomedical Sciences, University of Padova, Viale G. Colombo 3, 35131, Padova, Italy.
Curr Protein Pept Sci. 2013 Nov;14(7):635-40. doi: 10.2174/13892037113146660087.
Receptor tyrosine kinases (RTKs) are cell surface receptors that transmit extracellular signals to the interior of the cell activating multiple signaling cascades: the binding of specific extracellular ligands activates RTKs which act as a scaffold at plasma membrane level for the recruitment and activation of several signaling molecules. A paradigm shift emerged when an alternative direct signaling pathway was discovered: RTKs may move from cell surface to nucleus where they transduce the signals in a direct way. More recently, evidence has accumulated that RTKs may also translocate to mitochondria and regulate their functions, i.e., by altering tyrosine phosphorylation of specific mitochondrial proteins. This latter emerging pathway is here reviewed and discussed.
受体酪氨酸激酶(RTKs)是细胞表面受体,可将细胞外信号传递到细胞内部,激活多种信号级联反应:特定细胞外配体的结合激活 RTKs,后者在质膜水平作为支架,募集和激活多种信号分子。当发现一种替代的直接信号通路时,出现了一个范式转变:RTKs 可能从细胞膜转移到细胞核,在那里它们以直接的方式传递信号。最近,越来越多的证据表明,RTKs 也可能转移到线粒体并调节其功能,即通过改变特定线粒体蛋白的酪氨酸磷酸化。本文综述并讨论了这一新兴的途径。