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Cytokine-induced calgranulin C expression in keratocytes.细胞因子诱导角膜细胞中钙粒蛋白C的表达。
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Cloning and expression of human corneal calgranulin C (CO-Ag).人角膜钙粒蛋白C(CO-Ag)的克隆与表达
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钙粒蛋白C具有杀丝虫和抑制丝虫活性。

Calgranulin C has filariacidal and filariastatic activity.

作者信息

Gottsch J D, Eisinger S W, Liu S H, Scott A L

机构信息

Wilmer Ophthalmological Institute, School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.

出版信息

Infect Immun. 1999 Dec;67(12):6631-6. doi: 10.1128/IAI.67.12.6631-6636.1999.

DOI:10.1128/IAI.67.12.6631-6636.1999
PMID:10569784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC97076/
Abstract

The calgranulins are a family of calcium- and zinc-binding proteins produced by neutrophils, monocytes, and other cells. Calgranulins are released during inflammatory responses and have antimicrobial activity. Recently, one of the calgranulins, human calgranulin C (CaGC), has been implicated as an important component of the host responses that limit the parasite burden during filarial nematode infections. The goal of this work was to test the hypothesis that human CaGC has biologic activity against filarial parasites. Brugia malayi microfilariae and adults were exposed in vitro to 0.75 to 100 nM recombinant human CaGC. Recombinant CaGC affected adult and larval parasites in a dose-dependent fashion. Microfilariae were more sensitive to the action of CaGC than were adult parasites. At high levels, CaGC was both macrofilariacidal and microfilariacidal. At lower levels, the percentage of parasites killed was dependent on the level of CaGC in the culture system. The larvae not killed had limited motility. The filariastatic effect of low-level CaGC was reversed when the CaGC was removed from the culture system. Immunohistochemical analysis demonstrated that human CaGC accumulated in the cells of the hypodermis-lateral chord of adult and larval parasites. The antifilarial activity of CaGC was not due to the sequestration of zinc. Thus, the cellular and molecular mechanisms that result in the production and release of CaGC in humans may play a key role in the regulation of filarial parasite numbers.

摘要

钙粒蛋白是一类由中性粒细胞、单核细胞及其他细胞产生的钙结合和锌结合蛋白。钙粒蛋白在炎症反应期间释放,具有抗菌活性。最近,其中一种钙粒蛋白,即人钙粒蛋白C(CaGC),被认为是宿主反应的一个重要组成部分,在丝虫感染期间可限制寄生虫负荷。这项工作的目的是检验人CaGC对丝虫寄生虫具有生物活性这一假说。体外将马来布鲁线虫微丝蚴和成虫暴露于0.75至100 nM的重组人CaGC中。重组CaGC以剂量依赖方式影响成虫和幼虫寄生虫。微丝蚴比成虫寄生虫对CaGC的作用更敏感。在高浓度时,CaGC具有杀大丝虫和杀微丝蚴的作用。在较低浓度时,被杀寄生虫的百分比取决于培养系统中CaGC的水平。未被杀的幼虫活动受限。当从培养系统中去除CaGC时,低水平CaGC的丝虫抑制作用被逆转。免疫组织化学分析表明,人CaGC在成虫和幼虫寄生虫的皮下侧索细胞中积累。CaGC的抗丝虫活性并非由于锌的螯合作用。因此,导致人体中CaGC产生和释放的细胞和分子机制可能在丝虫寄生虫数量的调节中起关键作用。