کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3426763 | 1227343 | 2007 | 12 صفحه PDF | دانلود رایگان |

Human cytomegaloviruses (HCMVs) are important pathogens in immunocompromised patients and newborns. The viral chemokine, vCXCL-1, of the Toledo (Tol) strain of HCMV has been implicated in HCMV virulence. Chimpanzee CMV (CCMV) has several genes with similarity to the vCXCL-1Tol gene, UL146. In order to test whether the CCMV viral chemokine, vCXCL-1CCMV, is similar to vCXCL-1Tol, we characterized its function in vitro. Receptor binding, activation, chemotaxis, signaling, and apoptosis in neutrophils were compared between vCXCL-1Tol and vCXCL-1CCMV and host chemokines. Although the homologues had similar activation potentials, chemotactic properties, and signaling, vCXCL-1CCMV had a ∼ 70-fold lower affinity for CXCR2 and displayed differences in integrin upregulation and neutrophil apoptosis. These data demonstrate that in spite of extensive amino acid variability in vCXCL-1, CCMV may provide a model for assessing the role of vCXCL-1 in CMV pathogenesis in vivo.
Journal: Virology - Volume 364, Issue 2, 1 August 2007, Pages 454–465