GRK5 promotes F-actin bundling and targets bundles to membrane structures to control neuronal morphogenesis

被引:28
作者
Chen, Yuejun [1 ,2 ,3 ]
Wang, Feifei [1 ,2 ,3 ]
Long, Hui [1 ,2 ,3 ]
Chen, Ying [1 ,2 ,3 ]
Wu, Ziyan [1 ,2 ,3 ]
Ma, Lan [1 ,2 ,3 ]
机构
[1] Fudan Univ, State Key Lab Med Neurobiol, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Pharmacol Res Ctr, Shanghai 200032, Peoples R China
[3] Fudan Univ, Inst Brain Sci, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
COUPLED-RECEPTOR KINASES; DENDRITIC STRUCTURE; CYTOSKELETON; DYNAMICS; DOMAIN; ROLES; LOCALIZATION; FILOPODIA; PATHOLOGY; GUIDANCE;
D O I
10.1083/jcb.201104114
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neuronal morphogenesis requires extensive membrane remodeling and cytoskeleton dynamics. In this paper, we show that GRK5, a G protein-coupled receptor kinase, is critically involved in neurite outgrowth, dendrite branching, and spine morphogenesis through promotion of filopodial protrusion. Interestingly, GRK5 is not acting as a kinase but rather provides a key link between the plasma membrane and the actin cytoskeleton. GRK5 promoted filamentous actin (F-actin) bundling at the membranes of dynamic neuronal structures by interacting with both F-actin and phosphatidylinositol-4,5-bisphosphate. Moreover, separate domains of GRK5 mediated the coupling of actin cytoskeleton dynamics and membrane remodeling and were required for its effects on neuronal morphogenesis. Accordingly, GRK5 knockout mice exhibited immature spine morphology and deficient learning and memory. Our findings identify GRK5 as a critical mediator of dendritic development and suggest that coordinated actin cytoskeleton and membrane remodeling mediated by bifunctional actin-bundling and membrane-targeting molecules, such as GRK5, is crucial for proper neuronal morphogenesis and the establishment of functional neuronal circuitry.
引用
收藏
页码:905 / 920
页数:16
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