巨细胞病毒感染增强大鼠同种异体主动脉移植物中血小板源性生长因子- bb和转化生长因子- β 1 mRNA的表达。巨细胞病毒增强移植物动脉硬化的可能机制。

K B Lemström, P T Aho, C A Bruggeman, P J Häyry
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引用次数: 58

摘要

我们最近证明,大鼠巨细胞病毒(RCMV)感染诱导了外膜(血管周围炎)和内皮下空间(内皮炎)的早期炎症反应,以及DA (AG-B4, RT1a)和WF (AG-B2, RT1v)同种异体主动脉移植的平滑肌细胞(SMC)增殖加倍和内膜增厚。本研究探讨了RCMV感染对同种异体移植物外膜炎症结构和移植物血管壁SMC生长因子表达的影响。受体大鼠接种10(5)个RCMV Maastricht株形成斑块的U或未感染的大鼠作为对照。分别于移植后7天、1个月和3个月取出同种异体移植物,进行形态测定和免疫组织化学处理。分离RNA进行逆转录聚合酶链反应(RT-PCR)。RCMV感染与移植后7天同种异体外膜中T辅助细胞(W3/25)、T细胞毒性细胞(OX8)和自然杀伤细胞(3.2.3)的显著升高相关(P < 0.05),但此后无显著升高。rcmv感染的同种异体移植物中也存在较多的单核/巨噬细胞(OX42),但差异不显著。与此同时,RCMV感染显著增强了主要组织相容性复合体II类(OX6)的表达(P < 0.05),使白细胞介素- 2r (CD25)、细胞间粘附分子-1 (CD54;1A29)和淋巴细胞功能相关抗原-1 α链(CD11a;WT.1)外膜炎性浸润。RCMV感染与PDGF-BB mRNA在移植后7天(P < 0.05)和1个月(P < 0.025)以及转化生长因子- β 1 mRNA在移植后7天(P < 0.025)和1个月(P < 0.025)的早期显著表达有关。与未感染的同种异体移植物相比,移植后7天和1个月的RCMV感染以及1个月的表皮生长因子mRNA的上调不太明显(P < 0.05),尽管两组的mRNA表达均低于未移植DA主动脉的水平。RCMV感染后7天和1个月时,同种异体移植物血管壁碱性成纤维细胞生长因子mRNA表达量几乎增加了一倍。与未感染的同种异体移植物相比,RCMV感染对胰岛素样生长因子-1 mRNA表达没有额外的影响。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytomegalovirus infection enhances mRNA expression of platelet-derived growth factor-BB and transforming growth factor-beta 1 in rat aortic allografts. Possible mechanism for cytomegalovirus-enhanced graft arteriosclerosis.

We have recently demonstrated that rat cytomegalovirus (RCMV) infection induces an early inflammatory response in the adventitia (perivasculitis) and in the subendothelial space (endothelialitis) as well as doubles smooth muscle cell (SMC) proliferation and intimal thickening of rat aortic allografts performed from the DA (AG-B4, RT1a) to the WF (AG-B2, RT1v) strain. In this study, the impact of RCMV infection on the structure of inflammation in the allograft adventitia and on the expression of SMC growth factors in the allograft vascular wall was investigated. The recipient rats were inoculated with 10(5) plaque-forming U of RCMV Maastricht strain or left noninfected and used as controls. The allografts were removed at 7 days and 1 and 3 months after transplantation and processed for morphometry and immunohistochemistry. RNA was isolated for reverse transcriptase polymerase chain reaction (RT-PCR). RCMV infection was associated with significantly upregulated presence (P < .05) of T helper (W3/25), T cytotoxic (OX8), and natural killer (3.2.3) cells in the allograft adventitia 7 days after transplantation but not thereafter. More monocyte/macrophages (OX42) were also present in RCMV-infected allografts, but the difference was not significant. Concomitantly, RCMV infection significantly enhanced (P < .05) the expression of major histocompatibility complex class II (OX6) and almost doubled (P = NS) the expression of interleukin-2R (CD25), intercellular adhesion molecule-1 (CD54;1A29), and lymphocyte function-associated antigen-1 alpha-chain (CD11a; WT.1) in the adventitial inflammatory infiltrate. RCMV infection was linked with an early, prominent expression of both PDGF-BB mRNA at 7 days (P < .05) and at 1 month (P < .025) and of transforming growth factor-beta 1 mRNA at 7 days (P < .025) and at 1 month (P < .025) after transplantation. A less-prominent mRNA upregulation of acidic fibroblast growth factor (P < .05) was associated with RCMV infection at 7 days and at 1 month, as well as of epidermal growth factor at 1 month after transplantation, when compared with noninfected allografts, although the mRNA expression in both groups was below the levels of nontransplanted DA aortas. RCMV infection almost doubled basic fibroblast growth factor mRNA expression (P = NS) in the allograft vascular wall at 7 days and at 1 month. RCMV infection had no additional impact on insulin-like growth factor-1 mRNA expression when compared with noninfected allografts.(ABSTRACT TRUNCATED AT 400 WORDS)

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