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磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P)生成酶EhPIPKI在溶组织内阿米巴肌动蛋白动力学和吞噬作用中的新型调控作用

Novel regulatory roles of PtdIns(4,5)P generating enzyme EhPIPKI in actin dynamics and phagocytosis of Entamoeba histolytica.

作者信息

Sharma Shalini, Agarwal Shalini, Bharadwaj Ravi, Bhattacharya Sudha, Bhattacharya Alok

机构信息

School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.

School of Medicine, UMASS Medical School, Worcester, Massachusetts, USA.

出版信息

Cell Microbiol. 2019 Oct;21(10):e13087. doi: 10.1111/cmi.13087. Epub 2019 Jul 30.

Abstract

Motility and phagocytosis are the two important processes that are intricately linked to survival and virulence potential of the protist parasite Entamoeba histolytica. These processes primarily rely on actin-dependent pathways, and regulation of these pathways is critical for understanding the pathology of E. histolytica. Generally, phosphoinositides dynamics have not been explored in amoebic actin dynamics and particularly during phagocytosis in E. histolytica. We have explored the roles of PtdIns(4,5)P as well as the enzyme that produces this metabolite, EhPIPKI during phagocytosis. Immunofluorescence and live cell images showed enrichment of EhPIPKI in different stages of phagocytosis from initiation till the cups progressed towards closure. However, the enzyme was absent after phagosomes are pinched off from the membrane. Overexpression of a dominant negative mutant revealed a reduction in the formation of phagocytic cups and inhibition in the rate of engulfment of erythrocytes. Moreover, EhPIPKI binds directly to F and G-actin unlike PIPKs from other organisms. PtdIns(4,5)P , the product of the enzyme, also followed a similar distribution pattern during phagocytosis as determined by a GFP-tagged PH-domain from PLCδ, which specifically binds PtdIns(4,5)P in trophozoites. In summary, EhPIPKI regulates initiation of phagocytosis by regulating actin dynamics.

摘要

运动性和吞噬作用是与原生动物寄生虫溶组织内阿米巴的生存和致病潜力密切相关的两个重要过程。这些过程主要依赖于肌动蛋白依赖性途径,而这些途径的调控对于理解溶组织内阿米巴的病理学至关重要。一般来说,磷酸肌醇动力学在阿米巴肌动蛋白动力学中尚未得到探索,尤其是在溶组织内阿米巴的吞噬过程中。我们已经探索了磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P)以及产生这种代谢产物的酶——溶组织内阿米巴磷脂酰肌醇-4-磷酸5-激酶(EhPIPKI)在吞噬作用中的作用。免疫荧光和活细胞图像显示,从吞噬作用开始到吞噬杯向闭合发展的不同阶段,EhPIPKI都有富集。然而,吞噬体从膜上脱离后,该酶就不存在了。显性负性突变体的过表达显示吞噬杯的形成减少,红细胞吞噬速率受到抑制。此外,与其他生物体的磷脂酰肌醇-4-磷酸5-激酶不同,EhPIPKI直接与F-肌动蛋白和G-肌动蛋白结合。该酶的产物PtdIns(4,5)P在吞噬作用过程中也呈现出类似的分布模式,这是通过来自磷脂酶Cδ的绿色荧光蛋白标记的PH结构域确定的,该结构域特异性结合滋养体中的PtdIns(4,5)P。总之,EhPIPKI通过调节肌动蛋白动力学来调节吞噬作用的起始。

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