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介导盘基网柄菌趋化性的四条关键信号通路。

Four key signaling pathways mediating chemotaxis in Dictyostelium discoideum.

作者信息

Veltman Douwe M, Keizer-Gunnik Ineke, Van Haastert Peter J M

机构信息

Department of Molecular Cell Biology, University of Groningen, 9751 NN Haren, Netherlands.

出版信息

J Cell Biol. 2008 Feb 25;180(4):747-53. doi: 10.1083/jcb.200709180.

Abstract

Chemotaxis is the ability of cells to move in the direction of an external gradient of signaling molecules. Cells are guided by actin-filled protrusions in the front, whereas myosin filaments retract the rear of the cell. Previous work demonstrated that chemotaxis of unpolarized amoeboid Dictyostelium discoideum cells is mediated by two parallel pathways, phosphoinositide-3-kinase (PI3K) and phospholipase A2 (PLA2). Here, we show that polarized cells exhibit very good chemotaxis with inhibited PI3K and PLA2 activity. Using genetic screens, we demonstrate that this activity is mediated by a soluble guanylyl cyclase, providing two signals. The protein localizes to the leading edge where it interacts with actin filaments, whereas the cyclic guanosine monophosphate product induces myosin filaments in the rear of the cell. We conclude that chemotaxis is mediated by multiple signaling pathways regulating protrusions at the front and rear of the cell. Cells that express only rear activity are polarized but do not exhibit chemotaxis, whereas cells with only front signaling are unpolarized but undergo chemotaxis.

摘要

趋化性是细胞朝着信号分子外部梯度方向移动的能力。细胞由前端充满肌动蛋白的突起引导,而肌球蛋白丝则使细胞后端回缩。先前的研究表明,未极化的变形虫状盘基网柄菌细胞的趋化性由两条平行途径介导,即磷酸肌醇-3-激酶(PI3K)和磷脂酶A2(PLA2)。在此,我们表明极化细胞在PI3K和PLA2活性受到抑制的情况下仍表现出良好的趋化性。通过基因筛选,我们证明这种活性由可溶性鸟苷酸环化酶介导,产生两种信号。该蛋白定位于前沿,在那里它与肌动蛋白丝相互作用,而环磷酸鸟苷产物则诱导细胞后端的肌球蛋白丝。我们得出结论,趋化性由多种信号通路介导,这些信号通路调节细胞前端和后端的突起。仅表达后端活性的细胞是极化的,但不表现出趋化性,而仅具有前端信号的细胞是非极化的,但会发生趋化性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1a0/2265585/cf2e9817a146/jcb1800747f01.jpg

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