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- W176070669 abstract "Betaherpesviruses such as human cytomegalovirus (HCMV), human herpesvirus-6A and 6B (HHV-6), and human herpesvirus-7 (HHV-7) replicate more slowly than alphaherpesviruses, are highly species-specific for infection, and establish latency in progenitor cells of the bone marrow and monocytes of the blood. HCMV has been the prototype of the betaherpesviruses for studies of gene expression and regulation. In cell culture, HCMV strains have been adapted to preferentially infect and replicate in fibroblasts. However, low passage isolates replicate well in other cell types, such as endothelial cells, macrophages and dendritic cells. In the host, HCMV replicates in macrophages, dendritic cells, colonic and retinal pigmented epithelial cells, endothelial cells, fibroblasts, smooth muscle cells, neuronal cells, glial cells, hepatocytes, and trophoblasts (Fish et al., 1995, 1996; Hertel et al., 2003; Ibanez et al., 1991; Lathey and Spector, 1991; Maidji et al., 2002; Schmidbauer et al., 1989; Sinzger et al., 1993, 1995, 1996). In contrast, HHV-6 and HHV-7 infect CD4+ lymphocytes (Takahashi et al., 1989) as well as monocyte/macrophages. Although HCMV can be transferred into and out of polymorphonuclear leukocytes via cell-to-cell contact, these cells do not permit viral replication (Grundy et al., 1998; Sinclair and Sissons, 1996; Sinzger and Jahn, 1996)." @default.
- W176070669 created "2016-06-24" @default.
- W176070669 creator A5001885150 @default.
- W176070669 creator A5005763796 @default.
- W176070669 date "2007-08-16" @default.
- W176070669 modified "2023-10-17" @default.
- W176070669 title "Immediate–early CMV gene regulation and function" @default.
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