Monocyte apoptotic bodies are vehicles for influenza A virus propagation

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作者
Georgia K. Atkin-Smith
Mubing Duan
Damien J. Zanker
Liyen Loh
Thi H. O. Nguyen
Marios Koutsakos
Tien Nguyen
Xiangrui Jiang
Julio Carrera
Thanh Kha Phan
Chuanxin Liu
Stephanie Paone
Sara Oveissi
Amy L. Hodge
Amy A. Baxter
Katherine Kedzierska
Jason M. Mackenzie
Mark D. Hulett
Pamuk Bilsel
Weisan Chen
Ivan K. H. Poon
机构
[1] La Trobe Institute for Molecular Science,Department of Biochemistry and Genetics
[2] La Trobe University,Department of Microbiology and Immunology
[3] University of Melbourne,undefined
[4] at the Peter Doherty Institute for Infection and Immunity,undefined
[5] FluGen,undefined
[6] 597 Science Drive,undefined
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Communications Biology | / 3卷
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摘要
The disassembly of apoptotic cells into small membrane-bound vesicles termed apoptotic bodies (ApoBDs) is a hallmark of apoptosis; however, the functional significance of this process is not well defined. We recently discovered a new membrane protrusion (termed beaded apoptopodia) generated by apoptotic monocytes which fragments to release an abundance of ApoBDs. To investigate the function of apoptotic monocyte disassembly, we used influenza A virus (IAV) infection as a proof-of-concept model, as IAV commonly infects monocytes in physiological settings. We show that ApoBDs generated from IAV-infected monocytes contained IAV mRNA, protein and virions and consequently, could facilitate viral propagation in vitro and in vivo, and induce a robust antiviral immune response. We also identified an antipsychotic, Haloperidol, as an unexpected inhibitor of monocyte cell disassembly which could impair ApoBD-mediated viral propagation under in vitro conditions. Together, this study reveals a previously unrecognised function of apoptotic monocyte disassembly in the pathogenesis of IAV infections.
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