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一种非典型 EhGEF 通过 EhRho1 调节溶组织内阿米巴的吞噬作用。

An atypical EhGEF regulates phagocytosis in Entamoeba histolytica through EhRho1.

机构信息

Division of Infectious Diseases, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, United States of America.

Department of Biophysics, All India Institute of Medical Sciences, New Delhi, India.

出版信息

PLoS Pathog. 2021 Nov 22;17(11):e1010030. doi: 10.1371/journal.ppat.1010030. eCollection 2021 Nov.

Abstract

The parasite Entamoeba histolytica is the etiological agent of amoebiasis, a major cause of morbidity and mortality due to parasitic diseases in developing countries. Phagocytosis is an essential mode of obtaining nutrition and has been associated with the virulence behaviour of E. histolytica. Signalling pathways involved in activation of cytoskeletal dynamics required for phagocytosis remains to be elucidated in this parasite. Our group has been studying initiation of phagocytosis and formation of phagosomes in E. histolytica and have described some of the molecules that play key roles in the process. Here we showed the involvement of non-Dbl Rho Guanine Nucleotide Exchange Factor, EhGEF in regulation of amoebic phagocytosis by regulating activation of EhRho1. EhGEF was found in the phagocytic cups during the progression of cups, until closure of phagosomes, but not in the phagosomes themselves. Our observation from imaging, pull down experiments and down regulating expression of different molecules suggest that EhGEF interacts with EhRho1 and it is required during initiation of phagocytosis and phagosome formation. Also, biophysical, and computational analysis reveals that EhGEF mediates GTP exchange on EhRho1 via an unconventional pathway. In conclusion, we describe a non-Dbl EhGEF of EhRho1 which is involved in endocytic processes of E. histolytica.

摘要

寄生虫溶组织内阿米巴是阿米巴病的病原体,是发展中国家寄生虫病发病率和死亡率的主要原因。吞噬作用是获得营养的一种重要方式,与溶组织内阿米巴的毒力行为有关。在该寄生虫中,参与吞噬作用所必需的细胞骨架动力学激活的信号通路仍有待阐明。我们的研究小组一直在研究溶组织内阿米巴的吞噬作用起始和吞噬体的形成,并描述了在该过程中起关键作用的一些分子。在这里,我们通过调节 EhRho1 的激活,显示了非 Dbl Rho 鸟嘌呤核苷酸交换因子 EhGEF 在调节阿米巴吞噬作用中的作用。EhGEF 在杯体形成过程中存在于吞噬杯中,直到吞噬体闭合,但不存在于吞噬体本身中。我们的成像、下拉实验和下调不同分子表达的观察结果表明,EhGEF 与 EhRho1 相互作用,在吞噬作用起始和吞噬体形成过程中是必需的。此外,生物物理和计算分析表明 EhGEF 通过非传统途径介导 EhRho1 的 GTP 交换。总之,我们描述了 EhRho1 的非 Dbl EhGEF,它参与了溶组织内阿米巴的内吞作用过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d8e/8648123/f7b6e9dc04f6/ppat.1010030.g001.jpg

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