Lustigman S, McKerrow J H, Shah K, Lui J, Huima T, Hough M, Brotman B
Laboratory of Virology and Parasitology, The Lindsley F. Kimball Research Institute, New York Blood Center, New York, New York 10021, USA.
J Biol Chem. 1996 Nov 22;271(47):30181-9. doi: 10.1074/jbc.271.47.30181.
We have investigated the involvement of a cysteine protease in the development of Onchocerca volvulus fourth stage larvae (L4) by testing the effect of cysteine protease inhibitors on the survival of third stage larvae (L3), and the molting of L3 to L4 in vitro. When larvae were cultured in the presence of specific inhibitors, the peptidyl monofluoromethylketones, viability of either L3 or L4 was not affected. However, the inhibitors reduced the number of L3 that molted to L4 in vitro in a time- and dose-dependent manner. Molting was completely inhibited in the presence of 50-250 microM inhibitor. Ultrastructural examination of L3 that did not molt in the presence of inhibitors indicated that new L4 cuticle was synthesized, but there was no separation between the L3 and the L4 cuticles. The endogenous cysteine protease was detected in molting larvae after binding to labeled inhibitors, and by antibodies directed against a recombinant O. volvulus L3 cysteine protease that was cloned and expressed. The enzyme was detected in cuticle regions where the separation between the cuticles occurs in molting larvae. These studies suggest that molting and successful development of L4 depends on the expression and release of a cysteine protease.
我们通过测试半胱氨酸蛋白酶抑制剂对第三期幼虫(L3)存活以及L3体外蜕皮至第四期幼虫(L4)的影响,研究了一种半胱氨酸蛋白酶在盘尾丝虫第四期幼虫(L4)发育中的作用。当幼虫在特定抑制剂(肽基单氟甲基酮)存在的情况下培养时,L3或L4的活力均未受到影响。然而,这些抑制剂以时间和剂量依赖的方式减少了体外蜕皮至L4的L3数量。在存在50 - 250微摩尔抑制剂的情况下,蜕皮被完全抑制。对在抑制剂存在下未蜕皮的L3进行超微结构检查表明,新的L4表皮已合成,但L3和L4表皮之间没有分离。在与标记抑制剂结合后,以及通过针对克隆并表达的重组盘尾丝虫L3半胱氨酸蛋白酶的抗体,在蜕皮幼虫中检测到了内源性半胱氨酸蛋白酶。在蜕皮幼虫中表皮发生分离的表皮区域检测到了该酶。这些研究表明,L4的蜕皮和成功发育取决于半胱氨酸蛋白酶的表达和释放。