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基孔肯雅热感染的神经发病机制:星形胶质细胞增生与固有免疫激活

Neuropathogenesis of Chikungunya infection: astrogliosis and innate immune activation.

作者信息

Inglis Fiona M, Lee Kim M, Chiu Kevin B, Purcell Olivia M, Didier Peter J, Russell-Lodrigue Kasi, Weaver Scott C, Roy Chad J, MacLean Andrew G

机构信息

Tulane National Primate Research Center, Tulane Medical School, Covington, LA, 70433, USA.

Institute for Human Infections and Immunity, University of Texas Medical Branch, Galveston, TX, 77555-0610, USA.

出版信息

J Neurovirol. 2016 Apr;22(2):140-8. doi: 10.1007/s13365-015-0378-3. Epub 2015 Sep 29.

Abstract

Chikungunya, "that which bends up" in the Makonde dialect, is an emerging global health threat, with increasing incidence of neurological complications. Until 2013, Chikungunya infection had been largely restricted to East Africa and the Indian Ocean, with cases within the USA reported to be from foreign travel. However, in 2014, over 1 million suspected cases were reported in the Americas, and a recently infected human could serve as an unwitting reservoir for the virus resulting in an epidemic in the continental USA. Chikungunya infection is increasingly being associated with neurological sequelae. In this study, we sought to understand the role of astrocytes in the neuropathogenesis of Chikungunya infection. Even after virus has been cleared form the circulation, astrocytes were activated with regard to TLR2 expression. In addition, white matter astrocytes were hypertrophic, with increased arbor volume in gray matter astrocytes. Combined, these would alter the number and distribution of synapses that each astrocyte would be capable of forming. These results provide the first evidence that Chikungunya infection induces morphometric and innate immune activation of astrocytes in vivo. Perturbed glia-neuron signaling could be a major driving factor in the development of Chikungunya-associated neuropathology.

摘要

基孔肯雅热在马孔德方言中意为“弯曲起来”,是一种新出现的全球健康威胁,神经并发症的发病率不断上升。直到2013年,基孔肯雅热感染主要局限于东非和印度洋地区,美国报告的病例均来自国外旅行。然而,2014年,美洲报告了超过100万例疑似病例,近期感染的人类可能成为该病毒的潜在宿主,从而在美国本土引发疫情。基孔肯雅热感染与神经后遗症的关联日益密切。在本研究中,我们试图了解星形胶质细胞在基孔肯雅热感染神经发病机制中的作用。即使病毒已从循环中清除,星形胶质细胞的Toll样受体2(TLR2)表达仍被激活。此外,白质星形胶质细胞肥大,灰质星形胶质细胞的树突体积增加。综合起来,这些变化将改变每个星形胶质细胞能够形成的突触数量和分布。这些结果首次证明基孔肯雅热感染可在体内诱导星形胶质细胞的形态计量学变化和固有免疫激活。神经胶质细胞与神经元信号传导紊乱可能是基孔肯雅热相关神经病理学发展的主要驱动因素。

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