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疟原虫感染的红细胞通过外泌体样小泡进行细胞间通讯。

Cell-cell communication between malaria-infected red blood cells via exosome-like vesicles.

机构信息

Division of Infection and Immunity, the Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia.

出版信息

Cell. 2013 May 23;153(5):1120-33. doi: 10.1016/j.cell.2013.04.029. Epub 2013 May 15.

Abstract

Cell-cell communication is an important mechanism for information exchange promoting cell survival for the control of features such as population density and differentiation. We determined that Plasmodium falciparum-infected red blood cells directly communicate between parasites within a population using exosome-like vesicles that are capable of delivering genes. Importantly, communication via exosome-like vesicles promotes differentiation to sexual forms at a rate that suggests that signaling is involved. Furthermore, we have identified a P. falciparum protein, PfPTP2, that plays a key role in efficient communication. This study reveals a previously unidentified pathway of P. falciparum biology critical for survival in the host and transmission to mosquitoes. This identifies a pathway for the development of agents to block parasite transmission from the human host to the mosquito.

摘要

细胞间通讯是一种重要的信息交换机制,可促进细胞存活,控制种群密度和分化等特征。我们确定疟原虫感染的红细胞通过能够传递基因的类外泌体小泡在种群内的寄生虫之间直接进行通讯。重要的是,通过类外泌体小泡的通讯以表明信号参与的速度促进向有性形式的分化。此外,我们已经鉴定出一种疟原虫蛋白 PfPTP2,它在有效的通讯中起着关键作用。这项研究揭示了疟原虫生物学中以前未被识别的生存途径,对于在宿主和传播给蚊子中至关重要。这确定了一种阻断寄生虫从人类宿主传播到蚊子的途径。

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