Stephanopoulos D E, Kappes J C, Bernstein D I
The Division of Infectious Diseases, Children's Hospital Research Foundation Cincinnati, Ohio.
J Gen Virol. 1988 May;69 ( Pt 5):1079-83. doi: 10.1099/0022-1317-69-5-1079.
5-Azacytidine (5-AZC) reduces cytosine methylation in DNA and has been reported to activate quiescent virus genes. Treatment of explant cultures of latently herpes simplex virus type 2 (HSV-2)-infected guinea-pig dorsal root ganglia and spinal cords in vitro with 5-AZC significantly enhanced the rate of HSV recovery. Both the number of isolates from ganglia (P less than 0.001) and the rate of recovery (P less than 0.001) were significantly increased with the addition of 50 microM-5-AZC to explant cultures. Increased virus recovery appeared to be due to the induction of reactivation of latent virus, rather than an increase in replication, since 5-AZC inhibited HSV replication. These data support a role for methylation in HSV latency and reactivation.
5-氮杂胞苷(5-AZC)可降低DNA中的胞嘧啶甲基化,并且据报道能激活静止的病毒基因。在体外,用5-AZC处理潜伏感染2型单纯疱疹病毒(HSV-2)的豚鼠背根神经节和脊髓的外植体培养物,可显著提高HSV的恢复率。向外植体培养物中添加50微摩尔-5-AZC后,神经节分离株的数量(P小于0.001)和恢复率(P小于0.001)均显著增加。病毒恢复增加似乎是由于潜伏病毒的激活诱导,而非复制增加,因为5-AZC抑制HSV复制。这些数据支持甲基化在HSV潜伏和激活中的作用。