Predescu Sanda, Bardita Cristina, Predescu Dan
Departments of Pharmacology and Critical Care Medicine; Rush University Medical Center ; Chicago, IL USA.
Departments of Pharmacology and Critical Care Medicine; Rush University Medical Center ; Chicago, IL USA ; Department of Internal Medicine; Rush University Medical Center ; Chicago, IL USA.
Commun Integr Biol. 2015 Jun 24;8(3):e1034400. doi: 10.1080/19420889.2015.1034400. eCollection 2015 May-Jun.
Intersectin-1s (ITSN) is a ubiquitously expressed multifunctional protein known as a scaffold and regulator of the general endocytic machinery as well as a critical integrator of cellular signaling pathways. We showed recently that ITSN deficiency triggers a transforming growth factor β (TGFβ)/Alk5 signaling switch, from the canonical Smad 2/3 to the Erk1/2 MAPK pathway; moreover, endocytic impairment induced by ITSN deficiency enhances Alk5 ubiquitination and degradation and elicits TGFβ-paracrine effects mediated by circulating microparticles, leading to endothelial cell survival and increased proliferation. The studies expand our understanding of how ITSN facilitates cross-regulation of signaling pathways and provide insights into the involvement of ITSN deficiency in human disease.
相交蛋白-1s(ITSN)是一种广泛表达的多功能蛋白,作为一般内吞机制的支架和调节剂以及细胞信号通路的关键整合者而闻名。我们最近发现,ITSN缺乏会引发转化生长因子β(TGFβ)/Alk5信号转导开关,从经典的Smad 2/3途径转向Erk1/2 MAPK途径;此外,ITSN缺乏引起的内吞损伤会增强Alk5的泛素化和降解,并引发由循环微粒介导的TGFβ旁分泌效应,导致内皮细胞存活和增殖增加。这些研究扩展了我们对ITSN如何促进信号通路交叉调节的理解,并为ITSN缺乏在人类疾病中的作用提供了见解。