首页> 外文期刊>Journal of immunology research. >Crotalus durissus ruruima Snake Venom and a Phospholipase A2 Isolated from This Venom Elicit Macrophages to Form Lipid Droplets and Synthesize Inflammatory Lipid Mediators
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Crotalus durissus ruruima Snake Venom and a Phospholipase A2 Isolated from This Venom Elicit Macrophages to Form Lipid Droplets and Synthesize Inflammatory Lipid Mediators

机译:Crotalus ruruima蛇毒液和磷脂酶a2与该毒液孤立的巨噬细胞,形成脂液滴并合成炎症性脂质介质

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Viper snake Crotalus durissus ruruima (Cdr) is a subspecies found in northern area of Brazil. Among the snakes of Crotalus genus subspecies, the venom of Cdr presents highest level of crotoxin, which is the major component of Crotalus snake venoms, formed by two subunits (crotapotin and a phospholipase A2 named CBr) and presents potent neurotoxic activity. Curiously, the venom of C. d. ruruima (CdrV) is better neutralized by antibothropic than by anticrotalic serum, strongly suggesting that this venom has similarities with venom of Bothrops genus snakes with regard to the ability to induce inflammation. Macrophages are cells with a central role in inflammatory and immunological responses. Upon inflammatory stimuli, these cells exhibit increased numbers of lipid droplets, which are key organelles in the synthesis and release of inflammatory mediators. However, the effects of CdrV and CBr in macrophage functions are unknown. We herein investigated the ability of CdrV and CBr to activate macrophages with focus on the formation of lipid droplets (LDs), synthesis of lipid mediators, and mechanisms involved in these effects. The involvement of LDs in PGE2 biosynthesis was also assessed. Stimulation of murine macrophages with CdrV and CBr induced an increased number of LDs and release of prostanoids (PGE2, PGD2, and TXB2). Neither CdrV nor CBr induced the expression of COX-1 and COX-2 by macrophages. LDs induced by both CdrV and CBr are associated to PLIN2 recruitment and expression and were shown to be dependent on COX-1, but not COX-2 activity. Moreover, PGE2 colocalized to CdrV- and CBr-induced LDs, revealing the role of these organelles as sites for the synthesis of prostanoids. These results evidence, for the first time, the ability of a whole snake venom to induce formation of LDs and the potential role of these organelles for the production of inflammatory mediators during envenomation by Crotalus snakes.
机译:Viper Snake Crotalus Durissus Ruruima(CDR)是一家位于巴西北部地区的亚种。 CDR的蛇中,CDR的毒液呈现最高水平的曲妥嗪,其是由两个亚基(Crotapotin和磷脂酶A2命名CBR)形成的克罗塔属蛇毒液的主要成分,并呈现有效的神经毒性活性。好奇地,c的毒液d。 Ruruima(CDRV)由抗菌血清更好地中和,强烈暗示该毒液在诱导炎症的能力方面具有Bothrops属蛇的毒液的相似性。巨噬细胞是炎症和免疫反应中具有中心作用的细胞。在炎症刺激后,这些细胞表现出增加数量的脂液滴,其是炎性介质的合成和释放中的关键细胞器。然而,CDRV和CBR在巨噬细胞功能中的影响是未知的。我们在此研究CDRV和CBR激活巨噬细胞的能力,重点是脂质液滴(LDS),脂质介质的合成,以及参与这些效果的机制。还评估了LDS在PGE2生物合成中的参与。用CDRV和CBR刺激鼠巨噬细胞诱导增加的LD数量和前列腺素(PGE2,PGD2和TXB2)的释放。 CDRV和CBR都不诱导巨噬细胞COX-1和COX-2的表达。 CDRV和CBR诱导的LD与PLIN2募集和表达相关,并且被证明依赖于COX-1,但不是COX-2活性。此外,PGE2与CDRV-和CBR诱导的LDS分致大化,揭示了这些细胞器作为用于合成前列醇的位点的作用。这些结果证据是,首次证据了整个蛇毒毒液诱导LDS形成的能力以及这些细胞器在Crotalus Snakes encenomation期间生产炎症介质的潜在作用。

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