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局部接触毒液会引发水肿效应:酶的贡献和毒液金属蛋白酶的鉴定。

Topical Exposure to Venom Triggers Oedematogenic Effects: Enzymatic Contribution and Identification of Venom Metalloproteinase.

机构信息

Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Center for Ocean Mega-Science, Chinese Academy of Sciences, No. 7 Nanhai Road, Qingdao 266071, China.

Laboratory for Marine Drugs and Biological Products, Qingdao National Laboratory for Marine Science and Technology, No. 1 Wenhai Road, Qingdao 266237, China.

出版信息

Toxins (Basel). 2021 Jan 8;13(1):44. doi: 10.3390/toxins13010044.

DOI:10.3390/toxins13010044
PMID:33430137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7826907/
Abstract

Scyphozoan envenomation is featured as severe cutaneous damages due to the toxic effects of venom components released by the stinging nematocysts of a scyphozoan. However, the oedematogenic property and mechanism of scyphozoan venoms remain uninvestigated. Here, we present the oedematogenic properties of the nematocyst venom from (NnNV), a giant stinging scyphozoan in China, for the first time, using in vivo and in vitro models with class-specific inhibitors. NnNV was able to induce remarkable oedematogenic effects, including induction of significant oedema in the footpad and thigh of mouse, and increase in vascular permeability in the dorsal skin and kidney. Moreover, batimastat, a specific metalloproteinase inhibitor, could significantly reduce the Evan's blue leakage in the damaged organs and attenuate paw oedema after 12 h, but exerted no influence on NnNV-induced thigh oedema. These observations suggested a considerable contribution of NnNV metalloproteinase-like components to the increased vasopermeability, and the participation was strongly suggested to be mediated by destroying the integrity of the vascular basement membrane. Moreover, partial isolation combined LC-MS/MS profiling led to identification of the protein species Nn65 with remarkable metalloproteinase activity. This study contributes to the understanding of the effector components underlying the cutaneous damages induced by scyphozoan stings.

摘要

海葵蜇伤的特征是严重的皮肤损伤,这是由于海葵刺细胞释放的毒液成分的毒性作用所致。然而,海葵毒液的水肿形成特性和机制仍未得到研究。在这里,我们首次使用具有类特异性抑制剂的体内和体外模型,展示了来自中国大型海葵( )的刺细胞毒液的水肿形成特性。NnNV 能够诱导显著的水肿形成作用,包括在小鼠的足垫和大腿中诱导显著的水肿,以及在背部皮肤和肾脏中增加血管通透性。此外,batimastat,一种特异性金属蛋白酶抑制剂,可显著减少损伤器官中的伊文思蓝渗漏,并在 12 小时后减轻爪水肿,但对 NnNV 诱导的大腿水肿没有影响。这些观察结果表明,NnNV 金属蛋白酶样成分对增加血管通透性有相当大的贡献,并且强烈表明这种参与是通过破坏血管基底膜的完整性来介导的。此外,部分分离结合 LC-MS/MS 分析导致鉴定出具有显著金属蛋白酶活性的蛋白质 Nn65。本研究有助于理解海葵蜇伤引起的皮肤损伤的效应成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/9f63bf05d5c2/toxins-13-00044-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/94358ad38013/toxins-13-00044-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/ed634be548ee/toxins-13-00044-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/3c5653cf237b/toxins-13-00044-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/83f29c84b7b6/toxins-13-00044-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/0a1449ae6617/toxins-13-00044-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/4f557d1e4d16/toxins-13-00044-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/9f63bf05d5c2/toxins-13-00044-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/94358ad38013/toxins-13-00044-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/ed634be548ee/toxins-13-00044-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/3c5653cf237b/toxins-13-00044-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/83f29c84b7b6/toxins-13-00044-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/0a1449ae6617/toxins-13-00044-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/4f557d1e4d16/toxins-13-00044-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0acc/7826907/9f63bf05d5c2/toxins-13-00044-g007.jpg

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