Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA.
Maryland Pathogen Research Institute, University of Maryland, College Park, MD 20742, USA.
J Gen Virol. 2014 Apr;95(Pt 4):862-867. doi: 10.1099/vir.0.060558-0. Epub 2014 Jan 10.
The neuroinflammatory response to West Nile virus (WNV) infection can be either protective or pathological depending on the context. Although several studies have examined chemokine profiles within brains of WNV-infected mice, little is known about how various cell types within the central nervous system (CNS) contribute to chemokine expression. Here, we assessed chemokine expression in brain microvascular endothelial cells and astrocytes, which comprise the major components of the blood-brain barrier (BBB), in response to a non-pathogenic (WNV-MAD78) and a highly pathogenic (WNV-NY) strain of WNV. Higher levels of the chemokine CCL5 were detected in WNV-MAD78-infected brain endothelial monolayers compared with WNV-NY-infected cells. However, the opposite profile was observed in WNV-infected astrocytes, indicating that pathogenic and non-pathogenic strains of WNV provoke different CCL5 profiles at the BBB. Thus, cells comprising the BBB may contribute to a dynamic pro-inflammatory response within the CNS that evolves as WNV infection progresses.
西尼罗河病毒(WNV)感染引发的神经炎症反应可能具有保护作用,也可能具有病理作用,具体取决于具体情况。尽管已有多项研究检查了 WNV 感染小鼠大脑中的趋化因子谱,但对于中枢神经系统(CNS)内的各种细胞类型如何促成趋化因子表达,我们知之甚少。在这里,我们评估了脑微血管内皮细胞和星形胶质细胞(构成血脑屏障(BBB)的主要成分)对非致病性(WNV-MAD78)和高致病性(WNV-NY)WNV 株的趋化因子表达。与 WNV-NY 感染的细胞相比,WNV-MAD78 感染的脑内皮单层中检测到更高水平的趋化因子 CCL5。然而,在 WNV 感染的星形胶质细胞中观察到相反的模式,表明致病性和非致病性 WNV 株在 BBB 引发不同的 CCL5 谱。因此,构成 BBB 的细胞可能有助于随着 WNV 感染的进展,在 CNS 内产生动态的促炎反应。