Corticospinal circuit remodeling after central nervous system injury is dependent on neuronal activity

被引:29
作者
Bradley, Peter M. [1 ,2 ]
Denecke, Carmen K. [1 ,2 ,4 ]
Aljovic, Almir [1 ,2 ,4 ]
Schmalz, Anja [1 ,2 ]
Kerschensteiner, Martin [1 ,2 ,3 ]
Bareyre, Florence M. [1 ,2 ,3 ]
机构
[1] Ludwig Maximilians Univ Munchen, Univ Hosp, Inst Clin Neuroimmunol, Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Fac Med, Biomed Ctr, Martinsried, Germany
[3] Munich Cluster Syst Neurol SyNergy, Munich, Germany
[4] Ludwig Maximilians Univ Munchen, Grad Sch Syst Neurosci, Martinsried, Germany
基金
欧洲研究理事会;
关键词
LOCOMOTOR RECOVERY; FUNCTIONAL RECOVERY; PLASTICITY; CONNECTIONS; DREADDS; PROTEIN; FORMS;
D O I
10.1084/jem.20181406
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The remodeling of supraspinal axonal circuits mediates functional recovery after spinal cord injury. This process critically depends on the selection of appropriate synaptic connections between cortical projection and spinal relay neurons. To unravel the principles that guide this target selection, we used genetic and chemogenetic tools to modulate NMDA receptor (NMDAR) integrity and function, CREB-mediated transcription, and neuronal firing of relay neurons during injury-induced corticospinal remodeling. We show that NMDAR signaling and CREB-mediated transcription maintain nascent corticospinal tract (CST)-relay neuron contacts. These activity-dependent signals act during a defined period of circuit remodeling and do not affect mature or uninjured circuits. Furthermore, chemogenetic modulation of relay neuron activity reveals that the regrowing CST axons select their postsynaptic partners in a competitive manner and that preventing such activity-dependent shaping of corticospinal circuits limits motor recovery after spinal cord injury.
引用
收藏
页码:2503 / 2514
页数:12
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