Dumortier Jerome, Streblow Daniel N, Moses Ashlee V, Jacobs Jon M, Kreklywich Craig N, Camp David, Smith Richard D, Orloff Susan L, Nelson Jay A
Veterans Affairs, Portland VAMC, Portland, Oregon, USA.
J Virol. 2008 Jul;82(13):6524-35. doi: 10.1128/JVI.00502-08. Epub 2008 Apr 30.
Human cytomegalovirus (HCMV) is implicated in the acceleration of a number of vascular diseases including transplant vascular sclerosis (TVS), the lesion associated with chronic rejection (CR) of solid organ transplants. Although the virus persists in the allograft throughout the course of disease, few cells are directly infected by CMV. This observation is in contrast to the global effects that CMV has on the acceleration of TVS/CR, suggesting that CMV infection indirectly promotes the vascular disease process. Recent transcriptome analysis of CMV-infected heart allografts indicates that the virus induces cytokines and growth factors associated with angiogenesis (AG) and wound healing (WH), suggesting that CMV may accelerate TVS/CR through the induction and secretion of AG/WH factors from infected cells. We analyzed virus-free supernatants from HCMV-infected cells (HCMV secretomes) for growth factors, by mass spectrometry and immunoassays, and found that the HCMV secretome contains over 1,000 cellular proteins, many of which are involved in AG/WH. Importantly, functional assays demonstrated that CMV but not herpes simplex virus secretomes not only induce AG/WH but also promote neovessel stabilization and endothelial cell survival for 2 weeks. These findings suggest that CMV acceleration of TVS occurs through virus-induced growth factors and cytokines in the CMV secretome.
人巨细胞病毒(HCMV)与多种血管疾病的加速发展有关,包括移植血管硬化(TVS),这是一种与实体器官移植慢性排斥反应(CR)相关的病变。尽管病毒在疾病全过程中持续存在于同种异体移植物中,但很少有细胞被CMV直接感染。这一观察结果与CMV对TVS/CR加速发展的整体影响形成对比,提示CMV感染间接促进了血管疾病进程。最近对CMV感染的心脏同种异体移植物的转录组分析表明,该病毒可诱导与血管生成(AG)和伤口愈合(WH)相关的细胞因子和生长因子,提示CMV可能通过诱导和分泌感染细胞中的AG/WH因子来加速TVS/CR。我们通过质谱分析和免疫测定法,分析了来自HCMV感染细胞的无病毒上清液(HCMV分泌组)中的生长因子,发现HCMV分泌组包含1000多种细胞蛋白,其中许多与AG/WH有关。重要的是,功能测定表明,CMV而非单纯疱疹病毒的分泌组不仅可诱导AG/WH,还能促进新血管稳定和内皮细胞存活长达2周。这些发现提示,CMV通过其分泌组中病毒诱导的生长因子和细胞因子加速TVS的发生。