Activity-Dependent Regulation of Distinct Transport and Cytoskeletal Remodeling Functions of the Dendritic Kinesin KIF21B

被引:53
|
作者
Ghiretti, Amy E. [1 ]
Thies, Edda [2 ]
Tokito, Mariko K. [1 ]
Lin, Tianming [1 ]
Ostap, E. Michael [1 ]
Kneussel, Matthias [2 ]
Holzbaur, Erika L. F. [1 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Physiol, 415 Curie Blvd, Philadelphia, PA 19104 USA
[2] Univ Med Ctr Hamburg Eppendorf, ZMNH, Dept Mol Neurogenet, Falkenried 94, D-20251 Hamburg, Germany
关键词
MICROTUBULE GROWTH; BINDING PROTEIN; DYNAMIC INSTABILITY; NEURONAL-ACTIVITY; CULTURED NEURONS; PHOSPHORYLATION; TRAFFICKING; MECHANISMS; MOTORS; CREB;
D O I
10.1016/j.neuron.2016.10.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The dendritic arbor is subject to continual activity-dependent remodeling, requiring a balance between directed cargo trafficking and dynamic restructuring of the underlying microtubule tracks. How cytoskeletal components are able to dynamically regulate these processes to maintain this balance remains largely unknown. By combining single-molecule assays and live imaging in rat hippocampal neurons, we have identified the kinesin-4 KIF21B as a molecular regulator of activity-dependent trafficking and microtubule dynamicity in dendrites. We find that KIF21B contributes to the retrograde trafficking of brain-derived neurotrophic factor (BDNF)-TrkB complexes and also regulates microtubule dynamics through a separable, non-motor microtubule-binding domain. Neuronal activity enhances the motility of KIF21B at the expense of its role in cytoskeletal remodeling, the first example of a kinesin whose function is directly tuned to neuronal activity state. These studies suggest a model in which KIF21B navigates the complex cytoskeletal environment of dendrites by compartmentalizing functions in an activity-dependent manner.
引用
收藏
页码:857 / 872
页数:16
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