BRD4 inhibition attenuates inflammatory response in microglia and facilitates recovery after spinal cord injury in rats

被引:60
|
作者
Wang, Jianle [1 ,2 ,3 ,4 ]
Chen, Jiaoxiang [1 ,2 ,3 ,4 ]
Jin, Haiming [1 ,2 ,3 ,4 ]
Lin, Dongdong [3 ,4 ]
Chen, Yu [1 ,2 ,3 ,4 ]
Chen, Ximiao [5 ]
Wang, Ben [1 ,2 ,3 ,4 ]
Hu, Sunli [1 ,2 ,3 ,4 ]
Wu, Yan [6 ]
Wu, Yaosen [1 ,2 ,3 ,4 ]
Zhou, Yifei [1 ,2 ,3 ,4 ]
Tian, Naifeng [1 ,2 ,3 ,4 ]
Gao, Weiyang [1 ,2 ,3 ,4 ]
Wang, Xiangyang [1 ,2 ,3 ,4 ]
Zhang, Xiaolei [1 ,2 ,3 ,4 ,7 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 2, Dept Orthopaed, Wenzhou, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Yuying Childrens Hosp, Wenzhou, Zhejiang, Peoples R China
[3] Key Lab Orthopaed Zhejiang Prov, Wenzhou, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Sch Med 2, Wenzhou, Zhejiang, Peoples R China
[5] Guilin Med Coll, Affiliated Hosp, Dept Orthopaed, Guilin, Guangxi, Peoples R China
[6] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Orthopaed, Hangzhou, Zhejiang, Peoples R China
[7] Chinese Orthopaed Regenerat Med Soc, Wenzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
BRD4; inflammation; JQ1; microglia; spinal cord injury; NF-KAPPA-B; BROMODOMAIN; IDENTIFICATION; POLARIZATION; ACTIVATION; MECHANISMS; EXPRESSION; PATHWAYS; ALPHA; TLR4;
D O I
10.1111/jcmm.14196
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pathophysiology of spinal cord injury (SCI) involves primary injury and secondary injury. For the irreversibility of primary injury, therapies of SCI mainly focus on secondary injury, whereas inflammation is considered to be a major target for secondary injury; however the regulation of inflammation in SCI is unclear and targeted therapies are still lacking. In this study, we found that the expression of BRD4 was correlated with pro-inflammatory cytokines after SCI in rats; in vitro study in microglia showed that BRD4 inhibition either by lentivirus or JQ1 may both suppress the MAPK and NI-KB signalling pathways, which are the two major signalling pathways involved in inflammatory response in microglia. BRD4 inhibition by JQ1 not only blocked microglial M1 polarization, but also repressed the level of pro-inflammatory cytokines in microglia in vitro and in vivo. Furthermore, BRD4 inhibition by JQ1 can improve functional recovery and structural disorder as well as reduce neuron loss in SCI rats. Overall, this study illustrates that microglial BRD4 level is increased after SCI and BRD4 inhibition is able to suppress M1 polarization and pro-inflammatory cytokine production in microglia which ultimately promotes functional recovery after SCI.
引用
收藏
页码:3214 / 3223
页数:10
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