Seo Tadahiko, Sakon Taketo, Nakazawa Shiori, Nishioka Asuka, Watanabe Kohei, Matsumoto Kaori, Akasaka Mari, Shioi Narumi, Sawada Hitoshi, Araki Satohiko
Sugashima Marine Biological Laboratory, Graduate School of Science, Nagoya University, Japan.
Department of Chemistry, Faculty of Science, Fukuoka University, Japan.
FEBS J. 2017 Jun;284(11):1657-1671. doi: 10.1111/febs.14066. Epub 2017 Apr 20.
Snake venom metalloproteases (SVMPs) are members of the a disintegrin and metalloprotease (ADAM) family of proteins, as they possess similar domains. SVMPs are known to elicit snake venom-induced haemorrhage; however, the target proteins and cleavage sites are not known. In this work, we identified a target protein of vascular apoptosis-inducing protein 1 (VAP1), an SVMP, relevant to its ability to induce haemorrhage. VAP1 disrupted cell-cell adhesions by relocating VE-cadherin and γ-catenin from the cell-cell junction to the cytosol, without inducing proteolysis of VE-cadherin. The Wnt receptors low-density lipoprotein receptor-related proteins 5 and 6 (LRP5/6) are known to promote catenin relocation, and are rendered constitutively active in Wnt signalling by truncation. Thus, we examined whether VAP1 cleaves LRP5/6 to induce catenin relocation. Indeed, we found that VAP1 cleaved the extracellular region of LRP6 and LRP5. This cleavage removes four inhibitory β-propeller structures, resulting in activation of LRP5/6. Recombinant human ADAM8 and ADAM12 also cleaved LRP6 at the same site. An antibody against a peptide including the LRP6-cleavage site inhibited VAP1-induced VE-cadherin relocation and disruption of cell-cell adhesions in cultured cells, and blocked haemorrhage in mice in vivo. Intriguingly, animals resistant to the effects of haemorrhagic snake venom express variants of LRP5/6 that lack the VAP1-cleavage site, or low-density lipoprotein receptor domain class A domains involved in formation of the constitutively active form. The results validate LRP5/6 as physiological targets of ADAMs. Furthermore, they indicate that SVMP-induced cleavage of LRP5/6 causes disruption of cell-cell adhesion and haemorrhage, potentially opening new avenues for the treatment of snake bites.
蛇毒金属蛋白酶(SVMPs)是解整合素与金属蛋白酶(ADAM)蛋白家族的成员,因为它们具有相似的结构域。已知SVMPs会引发蛇毒诱导的出血;然而,其靶蛋白和切割位点尚不清楚。在这项研究中,我们鉴定出血管凋亡诱导蛋白1(VAP1,一种SVMP)的一种与出血诱导能力相关的靶蛋白。VAP1通过将血管内皮钙黏蛋白(VE- cadherin)和γ-连环蛋白从细胞间连接重新定位到细胞质中,破坏细胞间黏附,而不诱导VE- cadherin的蛋白水解。已知Wnt受体低密度脂蛋白受体相关蛋白5和6(LRP5/6)可促进连环蛋白的重新定位,并通过截短在Wnt信号传导中呈现组成性激活。因此,我们研究了VAP1是否切割LRP5/6以诱导连环蛋白重新定位。事实上,我们发现VAP1切割了LRP6和LRP5的细胞外区域。这种切割去除了四个抑制性β-螺旋桨结构,导致LRP5/6激活。重组人ADAM8和ADAM12也在相同位点切割LRP6。一种针对包含LRP6切割位点的肽的抗体抑制了VAP1诱导的VE- cadherin重新定位以及培养细胞中细胞间黏附的破坏,并在体内阻断了小鼠的出血。有趣的是,对出血性蛇毒作用具有抗性的动物表达缺乏VAP1切割位点的LRP5/6变体,或缺乏参与组成性激活形式形成的低密度脂蛋白受体A类结构域。这些结果证实LRP5/6是ADAMs的生理靶标。此外,它们表明SVMP诱导的LRP5/6切割会导致细胞间黏附破坏和出血,这可能为蛇咬伤的治疗开辟新途径。