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UNC-6/网蛋白和SLT-1/缝隙引导线索使由MIG-10/RIAM/片层状肌动蛋白结合蛋白介导的轴突生长定向。

UNC-6/netrin and SLT-1/slit guidance cues orient axon outgrowth mediated by MIG-10/RIAM/lamellipodin.

作者信息

Quinn Christopher C, Pfeil Douglas S, Chen Esteban, Stovall Elizabeth L, Harden Maegan V, Gavin Megan K, Forrester Wayne C, Ryder Elizabeth F, Soto Martha C, Wadsworth William G

机构信息

Department of Pathology, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA.

出版信息

Curr Biol. 2006 May 9;16(9):845-53. doi: 10.1016/j.cub.2006.03.025. Epub 2006 Mar 23.

Abstract

BACKGROUND

Axon migrations are guided by extracellular cues that can act as repellants or attractants. However, the logic underlying the manner through which attractive and repulsive responses are determined is unclear. Many extracellular guidance cues, and the cellular components that mediate their signals, have been implicated in both types of responses.

RESULTS

Genetic analyses indicate that MIG-10/RIAM/lamellipodin, a cytoplasmic adaptor protein, functions downstream of the attractive guidance cue UNC-6/netrin and the repulsive guidance cue SLT-1/slit to direct the ventral migration of the AVM and PVM axons in C. elegans. Furthermore, overexpression of MIG-10 in the absence of UNC-6 and SLT-1 induces a multipolar phenotype with undirected outgrowths. Addition of either UNC-6 or SLT-1 causes the neurons to become monopolar. Moreover, the ability of UNC-6 or SLT-1 to direct the axon ventrally is enhanced by the MIG-10 overexpression. We also demonstrate that an interaction between MIG-10 and UNC-34, a protein that promotes actin-filament extension, is important in the response to guidance cues and that MIG-10 colocalizes with actin in cultured cells, where it can induce the formation of lamellipodia.

CONCLUSIONS

We conclude that MIG-10 mediates the guidance of AVM and PVM axons in response to the extracellular UNC-6 and SLT-1 guidance cues. The attractive and repulsive guidance cues orient MIG-10-dependant axon outgrowth to cause a directional response.

摘要

背景

轴突迁移由细胞外信号引导,这些信号可作为排斥剂或吸引剂。然而,决定吸引和排斥反应方式的潜在逻辑尚不清楚。许多细胞外引导信号以及介导其信号的细胞成分与这两种反应都有关联。

结果

遗传分析表明,细胞质衔接蛋白MIG-10/RIAM/lamellipodin在秀丽隐杆线虫中吸引性引导信号UNC-6/netrin和排斥性引导信号SLT-1/slit的下游发挥作用,指导AVM和PVM轴突的腹侧迁移。此外,在没有UNC-6和SLT-1的情况下过表达MIG-10会诱导出具有无定向生长的多极表型。添加UNC-6或SLT-1会使神经元变为单极。而且,过表达MIG-10可增强UNC-6或SLT-1引导轴突腹侧生长的能力。我们还证明,MIG-10与促进肌动蛋白丝延伸的蛋白UNC-34之间的相互作用在对引导信号的反应中很重要,并且MIG-10在培养细胞中与肌动蛋白共定位,在那里它可以诱导片状伪足的形成。

结论

我们得出结论,MIG-10介导AVM和PVM轴突对细胞外UNC-6和SLT-1引导信号的反应。吸引和排斥性引导信号使依赖MIG-10的轴突生长定向,从而引起定向反应。

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