Araki Satohiko, Masuda Shinako, Maeda Hiroki, Ying Miao Jun, Hayashi Hiroshi
Marine Biological Laboratory, Graduate School of Science, Nagoya University, Toba, 517-0004, Mie, Japan.
Toxicon. 2002 May;40(5):535-42. doi: 10.1016/s0041-0101(01)00249-5.
Hemorrhagic snake venom induces apoptosis in vascular endothelial cells (VEC). In previous reports, we described the purification and cDNA cloning from Crotalus atrox of vascular apoptosis-inducing protein 1 (VAP1) that specifically induces apoptosis in VEC. VAP1 belongs to the metalloprotease/disintegrin family. Yet the mechanism of inducing apoptosis by VAP1 is still not known. Since other various metalloproteases and disintegrins in snake venoms are known to influence extracellular matrix and cell adhesion, we investigated here the involvement of these adhesion molecules in VAP1-induced apoptosis. Consequently, VAP1 induced apoptosis without degrading extracellular matrix or inhibiting adhesion of VEC. However, VAP1-induced apoptosis was inhibited by antibodies for integrin alpha3, alpha6, beta1. Additionally, apoptosis was inhibited by antibody for CD9, an integrin associated protein. These results suggest that integrins are involved in VAP1-induced apoptosis by some specific role rather than that of adhesion to extracellular matrix.
出血性蛇毒可诱导血管内皮细胞(VEC)凋亡。在先前的报道中,我们描述了从西部菱斑响尾蛇中纯化和克隆血管凋亡诱导蛋白1(VAP1),该蛋白可特异性诱导VEC凋亡。VAP1属于金属蛋白酶/解整合素家族。然而,VAP1诱导凋亡的机制仍不清楚。由于已知蛇毒中的其他各种金属蛋白酶和解整合素会影响细胞外基质和细胞黏附,我们在此研究了这些黏附分子在VAP1诱导凋亡中的作用。结果,VAP1诱导凋亡,但不降解细胞外基质或抑制VEC黏附。然而,VAP1诱导的凋亡被整合素α3、α6、β1的抗体抑制。此外,凋亡被整合素相关蛋白CD9的抗体抑制。这些结果表明,整合素通过某种特定作用而非与细胞外基质黏附的作用参与VAP1诱导的凋亡。