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<Emphasis Type="Italic">Mycobacterium marinum</Emphasis> Infection in Zebrafish and Microglia Imitates the Early Stage of Tuberculous Meningitis
Authors:Zhan Chen  Xiao-yi Shao  Chao Wang  Min-hui Hua  Cheng-niu Wang  Xin Wang  Qian-jin Wang  Jin-yi Yao  Yi-hui Fan  Yong-wei Qin
Institution:1.Department of Pathogenic Biology, Medical College,Nantong University,Nantong,China;2.Department of Immunology, Medical College,Nantong University,Nantong,China;3.Department of Obstetrics and Gynecology,Affiliated Hospital of Nantong University,Nantong,China;4.Basic Medical Research Center, Medical College,Nantong University,Nantong,China;5.Co-innovation Center of Neuroregeneration, Jiangsu Key Laboratory of Neuroregeneration,Nantong University,Nantong,China
Abstract:Mycobacterium tuberculosis (M. tuberculosis) invading and activating microglia causes the most serious subtypes of tuberculosis called tubercular meningitis. However, the developmental process of tubercular meningitis, especially the early phase, is poorly understood due to lacking well-established and well-accepted visible models in vitro and in vivo. Here, consistent with one recent report, we found Mycobacterium marinum (M. marinum) invade the zebrafish brain and subsequently cause granuloma-like structures. We further showed that M. marinum, which shares similar characteristics with M. tuberculosis, can invade microglia and replicate in microglia, which subsequently promote the secretion of pro-inflammatory cytokines such as IL-1β, IL-6, and TNF-α. M. marinum infection in microglia can also promote autophagy, which conversely limits the replication of M. marinum. Thus, pharmacological activation of autophagy by rapamycin could prevent M. marinum replication. Our study provides in vivo and in vitro models to study underlying pathogenic mechanisms of tubercular meningitis by using M. marinum. Our results also showed that activation of autophagy could be a meaningful way to prevent tubercular meningitis.
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