Microglia-Mediated Neuroimmune Response Regulates Cardiac Remodeling After Myocardial Infarction

被引:14
作者
Wang, Menglong [2 ,3 ,4 ]
Zhang, Jishou [2 ,3 ,4 ]
Yin, Zheng [2 ,3 ,4 ]
Ding, Wen [5 ]
Zhao, Mengmeng [2 ,3 ,4 ]
Liu, Jianfang [2 ,3 ,4 ]
Xu, Yao [2 ,3 ,4 ]
Xu, Shuwan [2 ,3 ,4 ]
Pan, Wei [2 ,3 ,4 ]
Wei, Cheng [2 ,3 ,4 ]
Jiang, Hong [1 ,2 ,3 ,4 ]
Wan, Jun [1 ,2 ,3 ,4 ]
机构
[1] Wuhan Univ, Dept Cardiol, Renmin Hosp, 238 Jiefang Rd, Wuhan 430060, Peoples R China
[2] Wuhan Univ, Dept Cardiol, Renmin Hosp, Wuhan, Peoples R China
[3] Wuhan Univ, Cardiovasc Res Inst, Wuhan, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Hubei Key Lab Cardiol, Sch Med, Hangzhou, Peoples R China
[5] Zhejiang Univ, Affiliated Hosp 1, Dept Radiol, Sch Med, Hangzhou, Peoples R China
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2023年 / 12卷 / 12期
基金
中国国家自然科学基金;
关键词
cardiac remodeling; microglia; myocardial infarction; neuroimmune response; PARAVENTRICULAR NUCLEUS; VENTRICULAR-ARRHYTHMIA; ACTIVATION; DYSFUNCTION; MODULATION; ISCHEMIA; DISEASE;
D O I
10.1161/JAHA.122.029053
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundSympathetic hyperactivity contributes to pathological remodeling after myocardial infarction (MI). However, the mechanisms underlying the increase in sympathetic activity remain unknown. Microglia are the predominant immune cells in the central nervous system and can regulate sympathetic neuron activity through neuroimmune response in the hypothalamic paraventricular nucleus. The present study aimed to investigate whether microglia-mediated neuroimmune response can regulate sympathetic activity and cardiac remodeling after MI. Methods and ResultsPLX3397 (pexidartinib) was used to deplete central microglia via intragastric injection or intracerebroventricular injection. After that, MI was induced by ligation of the left anterior descending coronary artery. Our study showed that MI resulted in the activation of microglia in the paraventricular nucleus. Microglia depletion, which was induced by PLX3397 treatment via intragastric injection or intracerebroventricular injection, improved cardiac function, reduced infarction size, and attenuated cardiomyocyte apoptosis, fibrosis, pathological electrical remodeling, and myocardial inflammation after MI. Mechanistically, these protective effects were associated with an attenuated neuroimmune response in the paraventricular nucleus, which contributed to the decrease of sympathetic activity and attenuation of sympathetic remodeling in the heart. However, intragastric injection with PLX3397 obviously depleted macrophages and induced neutrophil and T-lymphocyte disorders in the heart, blood, and spleen. ConclusionsMicroglia depletion in the central nervous system attenuates pathological cardiac remodeling after MI by inhibiting neuroimmune response and sympathetic activity. Intragastric administration of PLX3397 leads to serious deleterious effects in peripheral immune cells, especially macrophages, which should be a cause for concern in animal experiments and clinical practice.
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页数:37
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