Department of Molecular Pharmacology & Physiology, Byrd Alzheimer's Research Institute, University of South Florida, 4001 E. Fletcher Ave., Tampa, FL33613, USA.
Complex Carbohydrate Research Center, and Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, 30602, USA.
Sci Rep. 2022 Mar 14;12(1):4352. doi: 10.1038/s41598-022-08227-8.
Roundabout 4 (Robo4) is a transmembrane receptor that expresses specifically in endothelial cells. Soluble Robo4 was reported in the human plasma and mouse serum and is inhibitory towards FGF- and VEGF-induced angiogenesis. It remains unknown how soluble Robo4 is generated and if soluble Robo4 regulates additional angiogenic signaling. Here, we report soluble Robo4 is the product of constitutive ectodomain shedding of endothelial cell surface Robo4 by disintegrin metalloproteinases ADAM10 and ADAM17 and acts to inhibit angiogenic Slit3 signaling. Meanwhile, the ligand Slit3 induces cell surface receptor Robo4 endocytosis to shield Robo4 from shedding, showing Slit3 inhibits Robo4 shedding to enhance Robo4 signaling. Our study delineated ADAM10 and ADAM17 are Robo4 sheddases, and ectodomain shedding, including negative regulation by its ligand Slit3, represents a novel control mechanism of Robo4 signaling in angiogenesis.
Roundabout 4 (Robo4) 是一种跨膜受体,特异性表达于内皮细胞。已有研究报道人血浆和鼠血清中可溶性 Robo4 的存在,并证实其对 FGF- 和 VEGF 诱导的血管生成具有抑制作用。但可溶性 Robo4 的产生方式以及其是否调节其他血管生成信号通路仍不清楚。本研究报道了内皮细胞表面 Robo4 通过金属蛋白酶 ADAM10 和 ADAM17 的组成性外切酶脱落产生可溶性 Robo4,并抑制血管生成性 Slit3 信号。同时,配体 Slit3 诱导细胞表面受体 Robo4 内化,从而阻止 Robo4 脱落,表明 Slit3 通过抑制 Robo4 脱落来增强 Robo4 信号。本研究阐明 ADAM10 和 ADAM17 是 Robo4 的脱落酶,其配体 Slit3 通过外切酶脱落对 Robo4 进行负调控,这代表了血管生成中 Robo4 信号的一种新的调控机制。