Chichger Havovi, Braza Julie, Duong Huetran, Stark Myranda, Harrington Elizabeth O
Vascular Research Laboratory, Providence Veterans Affairs Medical Center, and Department of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island
Vascular Research Laboratory, Providence Veterans Affairs Medical Center, and Department of Medicine, Alpert Medical School of Brown University, Providence, Rhode Island.
Am J Physiol Lung Cell Mol Physiol. 2015 Oct 1;309(7):L700-9. doi: 10.1152/ajplung.00235.2015. Epub 2015 Aug 7.
Neovascularization, the formation of new blood vessels, requires multiple processes including vascular leak, migration, and adhesion. Endosomal proteins, such as Rabs, regulate trafficking of key signaling proteins involved in neovascularization. The novel endosome protein, p18, enhances vascular endothelial (VE)-cadherin recycling from early endosome to cell junction to improve pulmonary endothelial barrier function. Since endothelial barrier integrity is vital in neovascularization, we sought to elucidate the role for endosome proteins p18 and Rab4, Rab7, and Rab9 in the process of vessel formation within the pulmonary vasculature. Overexpression of wild-type p18 (p18(wt)), but not the nonendosomal-binding mutant (p18(N39)), significantly increased lung microvascular endothelial cell migration, adhesion, and both in vitro and in vivo tube formation. Chemical inhibition of mTOR or p38 attenuated the proneovascularization role of p18(wt). Similar to the effect of p18(wt), overexpression of prorecycling wild-type (Rab4(WT)) and endosome-anchored (Rab4(Q67L)) Rab4 enhanced neovascularization processes, whereas molecular inhibition of Rab4, by using the nonendosomal-binding mutant (Rab4(S22N)) attenuated VEGF-induced neovascularization. Unlike p18, Rab4-induced neovascularization was independent of mTOR or p38 inhibition but was dependent on p18 expression. This study shows for the first time that neovascularization within the pulmonary vasculature is dependent on the prorecycling endocytic proteins Rab4 and p18.
新生血管形成,即新血管的形成,需要包括血管渗漏、迁移和黏附在内的多个过程。内体蛋白,如Rabs,调节参与新生血管形成的关键信号蛋白的运输。新型内体蛋白p18可增强血管内皮(VE)-钙黏蛋白从早期内体到细胞连接的循环,以改善肺内皮屏障功能。由于内皮屏障的完整性在新生血管形成中至关重要,我们试图阐明内体蛋白p18和Rab4、Rab7及Rab9在肺血管系统内血管形成过程中的作用。野生型p18(p18(wt))而非非内体结合突变体(p18(N39))的过表达显著增加了肺微血管内皮细胞的迁移、黏附以及体外和体内的管腔形成。mTOR或p38的化学抑制减弱了p18(wt)的促血管生成作用。与p18(wt)的作用类似,促循环野生型(Rab4(WT))和内体锚定型(Rab4(Q67L))Rab4的过表达增强了新生血管形成过程,而使用非内体结合突变体(Rab4(S22N))对Rab4进行分子抑制则减弱了VEGF诱导的新生血管形成。与p18不同,Rab4诱导的新生血管形成不依赖于mTOR或p38抑制,但依赖于p18的表达。这项研究首次表明肺血管系统内的新生血管形成依赖于促循环的内吞蛋白Rab4和p18。