کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3392274 1592681 2011 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Intimal fibrosis in human cardiac allograft vasculopathy
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
پیش نمایش صفحه اول مقاله
Intimal fibrosis in human cardiac allograft vasculopathy
چکیده انگلیسی

Human Cardiac Allograft Vasculopathy (CAV) is one of the major complications for patients after heart transplantation. It is characterized by a concentric luminal narrowing due to (neo) intimal expansion in the coronary arteries of donor hearts after heart transplantation. In this process fibrosis plays an important role. Aim of this study is to analyze the factors and cells involved in this fibrotic process.Coronary arteries from five heart transplantation patients and three controls were obtained at autopsy. Quantitative real-time PCR was performed on mRNA obtained from various arterial layers isolated by laser micro dissection. Positive gene expression was confirmed by immunohistochemistry and/or in situ hybridisation.The strongest mRNA expression of fibrotic factors (predominantly pro-fibrotic) was found in the neo-intima. Especially, connective tissue growth factor expression was higher in the CAV vessels than in the controls. The lymphocyte activity of interferon gamma was only detected in CAV vessels. Furthermore as shown by in situ hybridisation, the lymphocytes producing interferon gamma also expressed transforming growth factor beta. Anti-fibrotic factors, such as bone morphogenic protein 4, were only expressed in CD3−/CD68− stromal cells. Macrophages present in the CAV and control vessels showed to be of the M2 type and did not produce any fibrotic factor(s).In conclusion, T-cells producing both interferon gamma and transforming growth factor beta, may play an important role in the fibrotic process in CAV vessels by upregulation of connective tissue growth factor production.


► We study fibrotic process in Coronary artery vasculopathy (CAV) after HTx.
► Laser microdissection is used to obtain tissue of CAV vessels for Q-PCR analysis.
► To identify proteins/mRNA immunohistochemistry and in situ hybridisation are used.
► mRNA of fibrotic factors is predominantly found in the neo-intima of CAV.
► IFN-γ and TGF-β production by T-cells may be responsible for the fibrotic process.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Transplant Immunology - Volume 25, Issues 2–3, September 2011, Pages 124–132
نویسندگان
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