Myosin II activity is required for structural plasticity at the axon initial segment

被引:32
作者
Evans, Mark D. [1 ,3 ]
Tufo, Candida [1 ]
Dumitrescu, Adna S. [1 ,4 ]
Grubb, Matthew S. [1 ,2 ]
机构
[1] Kings Coll London, Ctr Dev Neurobiol, London SE1 1UL, England
[2] FENS Kavli Network Excellence, Brussels, Belgium
[3] Gladstone Inst Neurol Dis, 1650 Owens St, San Francisco, CA 94158 USA
[4] CHU Pitie Salpetriere, Inst Cerveau & Moelle Epiniere, 83 Bld Hop, F-75013 Paris, France
基金
英国医学研究理事会; 英国惠康基金;
关键词
blebbistatin; cell culture; dentate granule cell; hippocampus; ACTIVITY-DEPENDENT RELOCATION; SYNAPTIC VESICLE ENDOCYTOSIS; ACTIN-FILAMENTS; HIPPOCAMPAL-NEURONS; CYTOSKELETON; INHIBITOR; DYNAMIN; TRANSCRIPTION; ARCHITECTURE; MATURATION;
D O I
10.1111/ejn.13597
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In neurons, axons possess a molecularly defined and highly organised proximal region - the axon initial segment (AIS) - that is a key regulator of both electrical excitability and cellular polarity. Despite existing as a large, dense structure with specialised cytoskeletal architecture, the AIS is surprisingly plastic, with sustained alterations in neuronal activity bringing about significant alterations to its position, length or molecular composition. However, although the upstream activity-dependent signalling pathways that lead to such plasticity have begun to be elucidated, the downstream mechanisms that produce structural changes at the AIS are completely unknown. Here, we use dissociated cultures of rat hippocampus to show that two forms of AIS plasticity in dentate granule cells-long-term relocation, and more rapid shortening - are completely blocked by treatment with blebbistatin, a potent and selective myosin II ATPase inhibitor. These data establish a link between myosin II and AIS function, and suggest that myosin II's primary role at the structure may be to effect activity-dependent morphological alterations.
引用
收藏
页码:1751 / 1757
页数:7
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