Francischetti Ivo M B, Mather Thomas N, Ribeiro José M C
Vector Biology Section, LMVR, NIAID, NIH, 12735 Twinbrook Parkway (Twinbrook III), Room 2E28, Rockville, MD 20892-8132, USA.
Thromb Haemost. 2005 Jul;94(1):167-74. doi: 10.1160/TH04-09-0566.
We report for the first time that saliva of the hard tick and Lyme disease vector, Ixodes scapularis, is a potent inhibitor of angiogenesis. Saliva (< or = 1:500 dilutions) or salivary gland (0.1-0.5 pairs/assay) dose-dependently inhibits microvascular endothelial cell (MVEC) proliferation. Inhibition was also detected with the saliva of the cattle tick Boophilus microplus but not with the salivary gland of Anopheles gambiae, An. stephensi, Lutzomyia longipalpis, Phlebotomus papatasi, Aedes aegypti, Culex quinquefasciatus, and Cimex lectularius. Inhibition of MVEC proliferation by I. Scapularis saliva was accompanied by a change in cell shape (shrinkage of the cytoplasm with loss of cell-cell interactions) and apoptosis which was estimated by expression of phosphatidylserine using the Apopercentage dye, and by a typical pattern of chromatin margination, condensation, and fragmentation as revealed by nuclear staining with Hoechst 33258. The effect of saliva appears to be mediated by endothelial cell alpha5beta1 integrin, because monoclonal antibodies against this but not alphavbeta3, alphavbeta5, alpha9beta1, or alpha2beta1 integrins remarkably block its effect. In addition, SDS/PAGE shows that saliva specifically degrades purified alpha5beta1 but not alphavbeta5 or alphavbeta3 integrins. Incubation of saliva with EDTA and 1,10-phenanthroline, but not phenylmethylsulfonyl fluoride (PMSF), inhibits saliva-dependent degradation of purified alpha5beta1 integrin, suggesting that a metalloprotease is responsible for the activity. Finally, saliva at < or = 1:1,000 dilutions blocks sprouting formation from chick embryo aorta implanted in Matrigel, an in vitro model of angiogenesis. These findings introduce the concept that tick saliva is a negative modulator of angiogenesis-dependent wound healing and tissue repair, therefore allowing ticks to feed for days. Inhibition of angiogenesis was hitherto an unidentified biologic property of the saliva of any blood-sucking arthropod studied so far. Its presence in tick saliva may be regarded as an additional source of angiogenesis inhibitors with potential applications for the study of both vector and vascular biology.
我们首次报告,硬蜱及莱姆病传播媒介肩突硬蜱的唾液是血管生成的强效抑制剂。唾液(≤1:500稀释度)或唾液腺(0.1 - 0.5对/试验)呈剂量依赖性抑制微血管内皮细胞(MVEC)增殖。微小牛蜱的唾液也检测到抑制作用,但冈比亚按蚊、斯氏按蚊、长须罗蛉、巴氏白蛉、埃及伊蚊、致倦库蚊和温带臭虫的唾液腺未检测到抑制作用。肩突硬蜱唾液对MVEC增殖的抑制伴随着细胞形态的改变(细胞质收缩,细胞间相互作用丧失)和凋亡,凋亡通过使用Apopercentage染料检测磷脂酰丝氨酸的表达以及用Hoechst 33258进行核染色所揭示的典型染色质边缘化、凝聚和断裂模式来估计。唾液的作用似乎是由内皮细胞α5β1整合素介导的,因为针对该整合素而非αvβ3、αvβ5、α9β1或α2β1整合素的单克隆抗体可显著阻断其作用。此外,SDS/PAGE显示唾液可特异性降解纯化的α5β1整合素,但不降解αvβ5或αvβ3整合素。唾液与EDTA和1,10 - 菲咯啉孵育可抑制唾液依赖性纯化α5β1整合素的降解,但与苯甲基磺酰氟(PMSF)孵育则无此作用,这表明金属蛋白酶负责该活性。最后,≤1:1000稀释度的唾液可阻断植入基质胶中的鸡胚主动脉的芽生形成,基质胶是血管生成的体外模型。这些发现引入了这样一个概念,即蜱唾液是血管生成依赖性伤口愈合和组织修复的负调节剂,从而使蜱能够吸食数天。血管生成抑制迄今是任何已研究的吸血节肢动物唾液中未被识别的生物学特性。其在蜱唾液中的存在可被视为血管生成抑制剂的额外来源,在媒介生物学和血管生物学研究中具有潜在应用价值。