Scott Erin P, Branigan Patrick J, Del Vecchio Alfred M, Weiss Susan R
Department of Microbiology, University of Pennsylvania, School of Medicine, Philadelphia, Pennsylvania 19104-6076, USA.
J Neurovirol. 2008 Jan;14(1):5-16. doi: 10.1080/13550280701750635.
Infection of mice with mouse hepatitis virus (MHV) strain JHM (RJHM) induces lethal encephalitis, with high macrophage and neutrophil, but minimal T-cell, infiltration into the brain when compared to the neuroattenuated strain RA59. To determine if chemokine expression corresponds with the cellular infiltrate, chemokine protein and RNA levels from the brains of infected mice were quantified. RJHM-infected mice had lower T-cell (CXCL9, CXCL10), but higher macrophage-attracting (CCL2), chemokine proteins compared to RA59. RJHM also induced significantly higher CXCL2 (a neutrophil chemoattractant) mRNA compared to RA59. The neurovirulent spike gene chimera SJHM/RA59 induces high levels of T cells and macrophages in the brain compared to the attenuated SA59/RJHM chimera. Accordingly, SJHM/RA59 induced higher levels of CXCL9, CXCL10, and CCL2 protein compared to SA59/RJHM. Chemokine mRNA patterns were in general agreement. Thus, chemokine patterns correspond with the cellular infiltrate, and the spike protein influences levels of macrophage, but not T-cell, chemokines.
用小鼠肝炎病毒(MHV)JHM株(RJHM)感染小鼠会诱发致死性脑炎,与神经减毒株RA59相比,感染后大脑中有大量巨噬细胞和中性粒细胞浸润,但T细胞浸润极少。为了确定趋化因子表达是否与细胞浸润相对应,对感染小鼠大脑中的趋化因子蛋白和RNA水平进行了定量分析。与RA59相比,RJHM感染的小鼠T细胞趋化因子(CXCL9、CXCL10)水平较低,但巨噬细胞趋化因子(CCL2)蛋白水平较高。与RA59相比,RJHM还诱导产生了显著更高水平的CXCL2(一种中性粒细胞趋化因子)mRNA。与减毒的SA59/RJHM嵌合体相比,神经毒力刺突基因嵌合体SJHM/RA59在大脑中诱导产生了高水平的T细胞和巨噬细胞。因此,与SA59/RJHM相比,SJHM/RA59诱导产生了更高水平的CXCL9、CXCL10和CCL2蛋白。趋化因子mRNA模式总体上与之相符。因此,趋化因子模式与细胞浸润相对应,刺突蛋白影响巨噬细胞趋化因子水平,但不影响T细胞趋化因子水平。