Ligoxygakis Petros, Pelte Nadège, Ji Chuanyi, Leclerc Vincent, Duvic Bernard, Belvin Marcia, Jiang Haobo, Hoffmann Jules A, Reichhart Jean-Marc
Institut de Biologie Moléculaire and Cellulaire, UPR 9022 du CNRS, 15, rue René Descartes, F-67084 Strasbourg Cedex, France.
EMBO J. 2002 Dec 2;21(23):6330-7. doi: 10.1093/emboj/cdf661.
A prominent response during the Drosophila host defence is the induction of proteolytic cascades, some of which lead to localized melanization of pathogen surfaces, while others activate one of the major players in the systemic antimicrobial response, the Toll pathway. Despite the fact that gain-of-function mutations in the Toll receptor gene result in melanization, a clear link between Toll activation and the melanization reaction has not been firmly established. Here, we present evidence for the coordination of hemolymph-borne melanization with activation of the Toll pathway in the Drosophila host defence. The melanization reaction requires Toll pathway activation and depends on the removal of the Drosophila serine protease inhibitor Serpin27A. Flies deficient for this serpin exhibit spontaneous melanization in larvae and adults. Microbial challenge induces its removal from the hemolymph through Toll-dependent transcription of an acute phase immune reaction component.
果蝇宿主防御过程中的一个显著反应是诱导蛋白水解级联反应,其中一些反应会导致病原体表面局部黑化,而其他反应则会激活全身抗菌反应的主要参与者之一——Toll途径。尽管Toll受体基因的功能获得性突变会导致黑化,但Toll激活与黑化反应之间的明确联系尚未得到确凿证实。在这里,我们提供证据表明,在果蝇宿主防御中,血淋巴介导的黑化与Toll途径的激活是协调进行的。黑化反应需要Toll途径的激活,并且依赖于果蝇丝氨酸蛋白酶抑制剂Serpin27A的清除。缺乏这种丝氨酸蛋白酶抑制剂的果蝇在幼虫和成虫阶段会出现自发黑化现象。微生物攻击通过急性期免疫反应成分的Toll依赖性转录诱导其从血淋巴中清除。