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Necl-5/PVR 增强 PDGF 诱导的生长微管向移动 NIH3T3 细胞前缘质膜的吸引力。

Necl-5/PVR enhances PDGF-induced attraction of growing microtubules to the plasma membrane of the leading edge of moving NIH3T3 cells.

机构信息

Division of Molecular and Cellular Biology, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine/Faculty of Medicine, Kobe, Hyogo, Japan.

出版信息

Genes Cells. 2010 Nov;15(11):1123-35. doi: 10.1111/j.1365-2443.2010.01450.x. Epub 2010 Oct 21.

Abstract

Microtubules (MTs) search for and grow toward the leading edge of moving cells, followed by their stabilization at a specific structure at the rear site of the leading edge. This dynamic re-orientation of MTs is critical to directional cell movement. We previously showed that Necl-5/poliovirus receptor (PVR) interacts with platelet-derived growth factor (PDGF) receptor and integrin α(v) β(3) at the leading edge of moving NIH3T3 cells, resulting in an enhancement of their directional movement. We studied here the role of Necl-5 in the PDGF-induced attraction of growing MTs to the leading edge of NIH3T3 cells. Necl-5 enhanced the PDGF-induced growth of MTs and attracted them near to the plasma membrane of the leading edge of NIH3T3 cells in an integrin α(v) β(3) -dependent manner. Furthermore, Necl-5 enhanced the PDGF-induced attraction of the plus-end-tracking proteins (+TIPs), including EB1, CLIP170, an intermediate chain subunit of cytoplasmic dynein, and p150(Glued) , a subunit of dynactin, near to the plasma membrane of the leading edge. Thus, Necl-5 plays a role in the attraction of growing MTs to the plasma membrane of the leading edge of moving cells.

摘要

微管(MTs)在移动细胞的前缘搜索并向其生长,随后在前缘的特定结构处稳定下来。这种 MT 的动态重定向对于细胞的定向运动至关重要。我们之前表明,Necl-5/脊髓灰质炎病毒受体(PVR)在移动的 NIH3T3 细胞的前缘与血小板衍生生长因子(PDGF)受体和整合素α(v)β(3)相互作用,导致其定向运动增强。在这里,我们研究了 Necl-5 在 PDGF 诱导的生长 MT 向 NIH3T3 细胞前缘吸引中的作用。Necl-5 增强了 PDGF 诱导的 MT 生长,并以整合素α(v)β(3)依赖性的方式将其吸引到 NIH3T3 细胞前缘的质膜附近。此外,Necl-5 增强了 PDGF 诱导的 +TIPs(包括 EB1、CLIP170、细胞质动力蛋白中间链亚基和 dynactin 的 p150(Glued))向移动细胞前缘质膜的吸引。因此,Necl-5 在将生长的 MT 吸引到移动细胞前缘的质膜中起作用。

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