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大鼠主动脉模型中的移植动脉硬化

Transplant arteriosclerosis in a rat aortic model.

作者信息

Isik F F, McDonald T O, Ferguson M, Yamanaka E, Gordon D

机构信息

Department of Pathology, University of Washington, Seattle.

出版信息

Am J Pathol. 1992 Nov;141(5):1139-49.

Abstract

Transplant arteriosclerosis (TA) has emerged as an obstacle to the long-term survival of transplanted organs, especially cardiac transplants. The animal models that have been used to study TA have not been fully characterized with regard to features such as the time course of cell proliferation and the sequence of cell types arriving in the developing intimal lesion. We present a model of TA based on a transplanted segment of abdominal aorta that helps address these questions. Two strains of rats (PVG x DA) underwent orthotopic aortic transplantation without immunosuppression and were killed at 14, 20, 40, and 60 days after transplantation. The within-strain control group displayed minimal evidence of cellular rejection with minimal to absent intimal lesions. In contrast, the allograft group showed a linearly increasing intimal lesion, up through 60 days after transplantation. The mechanism of intimal thickening was by an increase in cell number at the earlier time points with the later deposition of extracellular matrix. The early intimal lesion consisted mostly of mononuclear inflammatory cells (45%) with gradually increasing presence of smooth muscle cells (SMC) in the intima between 20 and 60 days. Conversely, the media showed gradual infiltration by macrophage-type cells with virtual loss of all SMC from the media by 40 days. The proliferative index showed a peak of 6% and 8% at 20 days in both the intima and media, respectively, and was preceded by the presence of macrophages. In fact, most of the proliferating cells at the earlier time points were either monocytes/macrophages, or were immediately adjacent to monocyte-/macrophage-rich regions. This straight artery segment model of transplant arteriosclerosis provides an easily quantifiable system in which the effects of different interventions (e.g., immunosuppressive regimens) can be tested.

摘要

移植性动脉硬化(TA)已成为移植器官长期存活的障碍,尤其是心脏移植。用于研究TA的动物模型在细胞增殖的时间进程以及到达发育中的内膜病变的细胞类型顺序等特征方面尚未得到充分表征。我们提出了一种基于腹主动脉移植段的TA模型,有助于解决这些问题。两组大鼠(PVG×DA)在未进行免疫抑制的情况下接受原位主动脉移植,并在移植后14、20、40和60天处死。同系对照组显示细胞排斥的证据极少,内膜病变轻微至无。相比之下,同种异体移植组的内膜病变呈线性增加,直至移植后60天。内膜增厚的机制是在早期时间点细胞数量增加,随后细胞外基质沉积。早期内膜病变主要由单核炎性细胞组成(45%),在20至60天之间内膜中平滑肌细胞(SMC)的存在逐渐增加。相反,中膜显示巨噬细胞型细胞逐渐浸润,到40天时中膜几乎所有SMC消失。增殖指数在内膜和中膜分别在20天时达到峰值6%和8%,且在巨噬细胞出现之前。事实上,在早期时间点大多数增殖细胞要么是单核细胞/巨噬细胞,要么紧邻富含单核细胞/巨噬细胞的区域。这种移植性动脉硬化的直动脉段模型提供了一个易于量化的系统,可用于测试不同干预措施(如免疫抑制方案)的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc00/1886661/4b5a4cb5f51f/amjpathol00083-0138-a.jpg

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