دورية أكاديمية

Myocardial Mitochondrial DNA Drives Macrophage Inflammatory Response through STING Signaling in Coxsackievirus B3-Induced Viral Myocarditis

التفاصيل البيبلوغرافية
العنوان: Myocardial Mitochondrial DNA Drives Macrophage Inflammatory Response through STING Signaling in Coxsackievirus B3-Induced Viral Myocarditis
المؤلفون: Andong Qin, Zhenke Wen, Sidong Xiong
المصدر: Cells, Vol 12, Iss 21, p 2555 (2023)
بيانات النشر: MDPI AG, 2023.
سنة النشر: 2023
المجموعة: LCC:Cytology
مصطلحات موضوعية: CVB3, VMC, mtDNA, STING, macrophage inflammatory response, Cytology, QH573-671
الوصف: Coxsackievirus B3 (CVB3), a single-stranded positive RNA virus, primarily infects cardiac myocytes and is a major causative pathogen for viral myocarditis (VMC), driving cardiac inflammation and organ dysfunction. However, whether and how myocardial damage is involved in CVB3-induced VMC remains unclear. Herein, we demonstrate that the CVB3 infection of cardiac myocytes results in the release of mitochondrial DNA (mtDNA), which functions as an important driver of cardiac macrophage inflammation through the stimulator of interferon genes (STING) dependent mechanism. More specifically, the CVB3 infection of cardiac myocytes promotes the accumulation of extracellular mtDNA. Such myocardial mtDNA is indispensable for CVB3-infected myocytes in that it induces a macrophage inflammatory response. Mechanistically, a CVB3 infection upregulates the expression of the classical DNA sensor STING, which is predominantly localized within cardiac macrophages in VMC murine models. Myocardial mtDNA efficiently triggers STING signaling in those macrophages, resulting in strong NF-kB activation when inducing the inflammatory response. Accordingly, STING-deficient mice are able to resist CVB3-induced cardiac inflammation, exhibiting minimal inflammation with regard to their functional cardiac capacities, and they exhibit higher survival rates. Moreover, our findings pinpoint myocardial mtDNA as a central element driving the cardiac inflammation of CVB3-induced VMC, and we consider the DNA sensor, STING, to be a promising therapeutic target for protecting against RNA viral infections.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 12212555
2073-4409
Relation: https://www.mdpi.com/2073-4409/12/21/2555; https://doaj.org/toc/2073-4409
DOI: 10.3390/cells12212555
URL الوصول: https://doaj.org/article/ea57aba156a94ae4bd2b5b927af09760
رقم الأكسشن: edsdoj.57aba156a94ae4bd2b5b927af09760
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:12212555
20734409
DOI:10.3390/cells12212555