Leishmania donovani mevalonate kinase regulates host actin for inducing phagocytosis

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Tanvir Bamra , Taj Shafi , Sushmita Das , Manjay Kumar , Pradeep Das
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Abstract

Despite the well-established role of macrophages in phagocytosing Leishmania, the contribution of the parasite to this process is not well understood. Present study provides insights into the mechanism underlying the MVK-induced entry of L. donovani and improve our knowledge of host-pathogen interactions. We have discussed Mevalonate kinase (MVK)-induced actin reorganization, modulation of signaling pathways and host cell functions. Our results show that LdMVK gains access to macrophage cytosol and induces actin assembly modulation through the activation of actin-related proteins: VASP, Src and ERM. We have also demonstrated that LdMVK induces Ca2+ signaling and Akt pathway in macrophages, which are critical components of Leishmania survival and proliferation. Interestingly, we found that antibodies against LdMVK can kill Leishmania-infected macrophages in culture by forming extracellular traps, highlighting the potential of LdMVK in inhibiting parasite death. Overall, LdMVK is a virulent factor in Leishmania that mediates parasite internalization and host modulation by targeting host proteins phosphorylation and calcium homeostasis having significant implications in disease progression.

唐氏利什曼原虫甲羟戊酸激酶调节宿主肌动蛋白以诱导吞噬作用
尽管巨噬细胞在吞噬利什曼原虫方面的作用已得到公认,但寄生虫在这一过程中的作用还不十分清楚。本研究深入探讨了 MVK 诱导唐诺瓦伊氏原虫进入巨噬细胞的机制,增进了我们对宿主与病原体相互作用的了解。我们讨论了甲羟戊酸激酶(MVK)诱导的肌动蛋白重组、信号通路调节和宿主细胞功能。我们的研究结果表明,LdMVK 能进入巨噬细胞胞体,并通过激活肌动蛋白相关蛋白诱导肌动蛋白组装调节:VASP、Src 和 ERM。我们还证明,LdMVK 能诱导巨噬细胞中的 Ca2+ 信号传导和 Akt 通路,这是利什曼病菌生存和增殖的关键要素。有趣的是,我们发现针对 LdMVK 的抗体可以通过形成细胞外陷阱杀死培养中受利什曼病感染的巨噬细胞,这凸显了 LdMVK 在抑制寄生虫死亡方面的潜力。总之,LdMVK 是利什曼病的一种致病因子,它通过靶向宿主蛋白磷酸化和钙稳态介导寄生虫内化和宿主调节,对疾病的进展有重要影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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