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蜡螟血淋巴中金属蛋白酶活性的识别与调控:介导体液免疫反应诱导的新途径。

Recognition and regulation of metalloproteinase activity in the haemolymph of Galleria mellonella: a new pathway mediating induction of humoral immune responses.

作者信息

Griesch J, Wedde M, Vilcinskas A

机构信息

Institute of Zoology, Free University of Berlin, Königin-Luise-Strasse 1-3, 14195, Berlin, Germany.

出版信息

Insect Biochem Mol Biol. 2000 Jun;30(6):461-72. doi: 10.1016/s0965-1748(00)00010-2.

Abstract

Proteolytic activity released within an organism by wounded tissues or invading pathogens can strongly impair the physiological homeostasis when it remains non-regulated. Thus, an efficient mechanism that enables recognition and inactivation of non-regulated proteolytic activity is essential to limit toxic effects. In larvae of the Greater wax moth Galleria mellonella we discovered that injection of bacterial thermolysin at a sublethal concentration mediates both acquired resistance against a subsequently injected lethal concentration of this metalloproteinase and stimulation of humoral immune response accompanied by the synthesis of an inducible metalloproteinase inhibitor (IMPI) which is released within the haemolymph. In search of a putative mechanism mediating recognition and regulation of released microbial metalloproteinases we determined that thermolysin-mediated hydrolysis of G. mellonella haemolymph proteins in vitro yields small (<3 kDa), heat-stable molecules which were discovered to represent potent elicitors of humoral immune responses when injected into untreated larvae. Obtained results allowed to design a model explaining for the first time regulation of released metalloproteinases within the haemolymph of insects. The determined coherence between regulation of released metalloproteinases by IMPI and the simultaneous induction of antimicrobial proteins provides a new insight into the mechanisms leading to expression of genes in course of humoral immune responses.

摘要

受伤组织或入侵病原体在生物体内释放的蛋白水解活性若不受调控,会严重破坏生理稳态。因此,一种能够识别并使不受调控的蛋白水解活性失活的有效机制对于限制毒性作用至关重要。在大蜡螟幼虫中,我们发现注射亚致死浓度的细菌嗜热菌蛋白酶既能介导对随后注射的致死浓度该金属蛋白酶产生获得性抗性,又能刺激体液免疫反应,同时伴随着血淋巴中可诱导金属蛋白酶抑制剂(IMPI)的合成与释放。为探寻介导识别和调控释放的微生物金属蛋白酶的潜在机制,我们确定嗜热菌蛋白酶在体外介导的大蜡螟血淋巴蛋白水解会产生小分子量(<3 kDa)、热稳定的分子,当将这些分子注射到未处理的幼虫体内时,发现它们是体液免疫反应的有效激发剂。所获结果使我们得以设计出一个首次解释昆虫血淋巴中释放的金属蛋白酶调控机制的模型。IMPI对释放的金属蛋白酶的调控与抗菌蛋白的同时诱导之间的确定关联,为体液免疫反应过程中基因表达机制提供了新的见解。

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