Microglia Are Indispensable for Synaptic Plasticity in the Spinal Dorsal Horn and Chronic Pain

被引:164
|
作者
Zhou, Li-Jun [1 ,2 ,3 ,4 ]
Peng, Jiyun [3 ,5 ]
Xu, Ya-Nan [1 ,2 ]
Zeng, Wei-Jie [1 ,2 ]
Zhang, Jun [1 ,2 ]
Wei, Xiao [1 ,2 ]
Mai, Chun-Lin [1 ,2 ]
Lin, Zhen-Jia [1 ,2 ]
Liu, Yong [3 ,5 ]
Murugan, Madhuvika [3 ,5 ]
Eyo, Ukpong B. [3 ,5 ]
Umpierre, Anthony D. [5 ]
Xin, Wen-Jun [1 ,2 ,4 ]
Chen, Tao [6 ,7 ]
Li, Mingtao [4 ]
Wang, Hui [8 ,9 ]
Richardson, Jason R. [10 ]
Tan, Zhi [1 ,2 ]
Liu, Xian-Guo [1 ,2 ,4 ]
Wu, Long-Jun [3 ,5 ,11 ,12 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Physiol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Zhongshan Sch Med, Pain Res Ctr, Guangzhou 510080, Guangdong, Peoples R China
[3] Rutgers State Univ, Dept Cell Biol & Neurosci, Piscataway, NJ 08854 USA
[4] Guangdong Prov Key Lab Brain Funct & Dis, Guangzhou 510080, Guangdong, Peoples R China
[5] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
[6] Fourth Mil Med Univ, Dept Anat Histol & Embryol, Xian 710032, Shaanxi, Peoples R China
[7] Fourth Mil Med Univ, KK Leung Brain Res Ctr, Xian 710032, Shaanxi, Peoples R China
[8] Rutgers Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ 08854 USA
[9] Nantong Univ, Sch Pharm, Dept Pharmacol, Nantong 22600, Peoples R China
[10] Florida Int Univ, Dept Environm Hlth Sci, Miami, FL 33199 USA
[11] Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
[12] Mayo Clin, Dept Immunol, Rochester, MN 55905 USA
来源
CELL REPORTS | 2019年 / 27卷 / 13期
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
LONG-TERM POTENTIATION; FIBER-EVOKED POTENTIALS; GENE-RELATED PEPTIDE; NEUROTROPHIC FACTOR; ROOT GANGLIA; KAPPA-B; CORD; HYPERSENSITIVITY; ACTIVATION; MODEL;
D O I
10.1016/j.celrep.2019.05.087
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Spinal long-term potentiation (LTP) at C-fiber synapses is hypothesized to underlie chronic pain. However, a causal link between spinal LTP and chronic pain is still lacking. Here, we report that high-frequency stimulation (HFS; 100 Hz, 10 V) of the mouse sciatic nerve reliably induces spinal LTP without causing nerve injury. LTP-inducible stimulation triggers chronic pain lasting for more than 35 days and increases the number of calcitonin gene-related peptide (CGRP) terminals in the spinal dorsal horn. The behavioral and morphological changes can be prevented by blocking NMDA receptors, ablating spinal microglia, or conditionally deleting microglial brain-derived neurotrophic factor (BDNF). HFS-induced spinal LTP, microglial activation, and upregulation of BDNF are inhibited by antibodies against colony-stimulating factor 1 (CSF-1). Together, our results show that microglial CSF1 and BDNF signaling are indispensable for spinal LTP and chronic pain. The microglia-dependent transition of synaptic potentiation to structural alterations in pain pathways may underlie pain chronicity.
引用
收藏
页码:3844 / +
页数:22
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