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质膜突起介导 诱导的宿主细胞-细胞融合。

Plasma membrane protrusions mediate host cell-cell fusion induced by .

机构信息

Department of Molecular & Cell Biology, University of California, Berkeley, Berkeley, CA 94720.

出版信息

Mol Biol Cell. 2022 Jul 1;33(8):ar70. doi: 10.1091/mbc.E22-02-0056. Epub 2022 May 20.

Abstract

Cell-cell fusion is important for biological processes including fertilization, development, immunity, and microbial pathogenesis. Bacteria in the pseudomallei group of the species, including , spread between host cells by inducing cell-cell fusion. Previous work showed that -induced cell-cell fusion requires intracellular bacterial motility and a bacterial protein secretion apparatus called the type VI secretion system-5 (T6SS-5), including the T6SS-5 protein VgrG5. However, the cellular-level mechanism of and T6SS-5 proteins important for bacteria-induced cell-cell fusion remained incompletely described. Using live-cell imaging, we found bacteria used actin-based motility to push on the host cell plasma membrane to form plasma membrane protrusions that extended into neighboring cells. Then, membrane fusion occurred within membrane protrusions either proximal to the bacterium at the tip or elsewhere within protrusions. Expression of VgrG5 by bacteria within membrane protrusions was required to promote cell-cell fusion. Furthermore, a second predicted T6SS-5 protein, TagD5, was also required for cell-cell fusion. In the absence of VgrG5 or TagD5, bacteria in plasma membrane protrusions were engulfed into neighboring cells. Our results suggest that the T6SS-5 effectors VgrG5 and TagD5 are secreted within membrane protrusions and act locally to promote membrane fusion.

摘要

细胞融合对于包括受精、发育、免疫和微生物发病机制在内的生物过程很重要。类鼻疽假单胞菌群中的细菌,包括 ,通过诱导细胞融合在宿主细胞之间传播。先前的工作表明,诱导的细胞融合需要细菌的胞内运动和一种称为六型分泌系统-5(T6SS-5)的细菌蛋白分泌装置,包括 T6SS-5 蛋白 VgrG5。然而,细菌诱导的细胞融合的细胞水平机制和 T6SS-5 蛋白仍未完全描述。通过活细胞成像,我们发现细菌利用肌动蛋白依赖性运动推动宿主细胞膜形成延伸到邻近细胞的质膜突起。然后,质膜突起内的膜融合发生在靠近细菌尖端的突起处或突起内的其他部位。细菌在质膜突起内表达 VgrG5 是促进细胞融合所必需的。此外,第二个预测的 T6SS-5 蛋白 TagD5 也需要细胞融合。在没有 VgrG5 或 TagD5 的情况下,质膜突起内的细菌被邻近细胞吞噬。我们的结果表明,T6SS-5 效应物 VgrG5 和 TagD5 被分泌到质膜突起内,并在局部发挥作用促进膜融合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9033/9635284/b1e4c859d797/mbc-33-ar70-g001.jpg

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