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来自矛头蝮蛇毒液的一种解整合素样蛋白 Alternagin-C,可减轻炎症和血管生成,并刺激小鼠海绵诱导的纤维血管组织中的胶原沉积。

Alternagin-C, a disintegrin-like protein from Bothrops alternatus venom, attenuates inflammation and angiogenesis and stimulates collagen deposition of sponge-induced fibrovascular tissue in mice.

机构信息

Departamento de Ciências Fisiológicas, Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, UFU, Uberlândia, MG, Brazil.

Departamento de Ciências Fisiológicas, Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, UFU, Uberlândia, MG, Brazil.

出版信息

Int J Biol Macromol. 2019 Nov 1;140:653-660. doi: 10.1016/j.ijbiomac.2019.08.171. Epub 2019 Aug 20.

Abstract

Alternagin-C (ALT-C), a disintegrin-like protein obtained from the venom of Bothrops alternatus, is able to modulate cellular behaviors such as adhesion, migration and proliferation, as well as the production of various growth factors via αβ integrin, important processes during inflammation, angiogenesis and fibrogenesis, which although appear as distinct events, act concomitantly in several chronic inflammatory diseases. Our objective was to investigate the effects of ALT-C on components of the sponge-induced inflammatory response in balb/c mice. The polyester-polyurethane sponges were implanted in mice's subcutaneous layer of the dorsal region and daily injected with saline (control group) or ALT-C (10, 100 or 1000 ng). Nine days after implantation the implants were removed and processed. ALT-C inhibited the inflammatory response, observed through mast cell reduction, NAG-activity and also by the inhibition of TNF-α, CXCL-1 and CCL2/JE/MCP-1 cytokines. ALT-C was also able to reduce hemoglobin content, number of vessels and the concentrations of VEGF and FGF cytokines. Finally, at its highest dose (1000 ng), ALT-C increased all evaluated markers associated with fibrogenesis (collagen production and TGF-β1 levels). All these factors reveal that ALT-C is a strong candidate to be exploited in the development of anti-inflammatory and anti-angiogenic therapies in chronic inflammatory processes.

摘要

交替蛋白-C(ALT-C)是从矛头蝮蛇(Bothrops alternatus)毒液中提取的一种解整合素样蛋白,能够通过 αβ 整合素调节细胞行为,如黏附、迁移和增殖,以及各种生长因子的产生,这些过程在炎症、血管生成和纤维化过程中非常重要,尽管这些过程看起来是不同的事件,但在几种慢性炎症性疾病中同时发生。我们的目的是研究 ALT-C 对 BALB/c 小鼠海绵体诱导的炎症反应成分的影响。聚酯-聚亚安酯海绵被植入小鼠背部皮下层,并每天注射生理盐水(对照组)或 ALT-C(10、100 或 1000ng)。植入 9 天后,取出植入物并进行处理。ALT-C 通过减少肥大细胞、NAG 活性以及抑制 TNF-α、CXCL-1 和 CCL2/JE/MCP-1 细胞因子来抑制炎症反应。ALT-C 还能够降低血红蛋白含量、血管数量以及 VEGF 和 FGF 细胞因子的浓度。最后,在其最高剂量(1000ng)时,ALT-C 增加了所有与纤维化相关的评估标志物(胶原产生和 TGF-β1 水平)。所有这些因素表明,ALT-C 是开发慢性炎症过程中抗炎和抗血管生成疗法的有力候选物。

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