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Monocyte-Derived Macrophages Aggravate Cardiac Dysfunction After Ischemic Stroke in Mice.
Lin, Hong-Bin; Hong, Pu; Yin, Meng-Yu; Yao, Zhi-Jun; Zhang, Jin-Yu; Jiang, Yan-Pin; Huang, Xuan-Xuan; Xu, Shi-Yuan; Li, Feng-Xian; Zhang, Hong-Fei.
Afiliación
  • Lin HB; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Hong P; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Yin MY; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Yao ZJ; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Zhang JY; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science Guangzhou Guangdong China.
  • Jiang YP; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Huang XX; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Xu SY; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Li FX; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
  • Zhang HF; Department of Anesthesiology, Zhujiang Hospital Southern Medical University Guangzhou Guangdong China.
J Am Heart Assoc ; 13(9): e034731, 2024 May 07.
Article en En | MEDLINE | ID: mdl-38700011
ABSTRACT

BACKGROUND:

Cardiac damage induced by ischemic stroke, such as arrhythmia, cardiac dysfunction, and even cardiac arrest, is referred to as cerebral-cardiac syndrome (CCS). Cardiac macrophages are reported to be closely associated with stroke-induced cardiac damage. However, the role of macrophage subsets in CCS is still unclear due to their heterogeneity. Sympathetic nerves play a significant role in regulating macrophages in cardiovascular disease. However, the role of macrophage subsets and sympathetic nerves in CCS is still unclear. METHODS AND

RESULTS:

In this study, a middle cerebral artery occlusion mouse model was used to simulate ischemic stroke. ECG and echocardiography were used to assess cardiac function. We used Cx3cr1GFPCcr2RFP mice and NLRP3-deficient mice in combination with Smart-seq2 RNA sequencing to confirm the role of macrophage subsets in CCS. We demonstrated that ischemic stroke-induced cardiac damage is characterized by severe cardiac dysfunction and robust infiltration of monocyte-derived macrophages into the heart. Subsequently, we identified that cardiac monocyte-derived macrophages displayed a proinflammatory profile. We also observed that cardiac dysfunction was rescued in ischemic stroke mice by blocking macrophage infiltration using a CCR2 antagonist and NLRP3-deficient mice. In addition, a cardiac sympathetic nerve retrograde tracer and a sympathectomy method were used to explore the relationship between sympathetic nerves and cardiac macrophages. We found that cardiac sympathetic nerves are significantly activated after ischemic stroke, which contributes to the infiltration of monocyte-derived macrophages and subsequent cardiac dysfunction.

CONCLUSIONS:

Our findings suggest a potential pathogenesis of CCS involving the cardiac sympathetic nerve-monocyte-derived macrophage axis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Modelos Animales de Enfermedad / Proteína con Dominio Pirina 3 de la Familia NLR / Accidente Cerebrovascular Isquémico / Macrófagos / Ratones Endogámicos C57BL Límite: Animals Idioma: En Revista: J Am Heart Assoc Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Modelos Animales de Enfermedad / Proteína con Dominio Pirina 3 de la Familia NLR / Accidente Cerebrovascular Isquémico / Macrófagos / Ratones Endogámicos C57BL Límite: Animals Idioma: En Revista: J Am Heart Assoc Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido