Kim Won-Jung, Kang Yoon-Joong, Suk Kyoungho, Park Jeong-Euy, Kwon Byoung S, Lee Won-Ha
Department of Genetic Engineering, School of Life Sciences and Biotechnology School of Medicine, Kyungpook National University, Daegu, Korea.
Immunol Invest. 2008;37(4):359-73. doi: 10.1080/08820130802123139.
Members of the TNFSF/TNFRSF are involved in the immunoregulation of various immune reactions and diseases. Recently, LIGHT/TR2, GITRL/GITR, and TL1A/DR3 have been reported as playing roles in the inflammatory reactions in atherosclerosis, but a comparative analysis of these molecules has not been conducted. In order to compare their expression patterns, immunohistochemical analyses were performed using six human carotid endoarterectomy samples. The expression of these molecules was detected in the various cell types that constitute atherosclerotic plaques. The expression of all analyzed molecules was detected, albeit at various levels, mainly in foamy macrophages in all tested samples. The strong expression of these molecules in endothelial and smooth muscle cells was also detected in 2 and 1 plaque samples, respectively, while others express only some of the tested molecules. Flow cytometry analyses of human monocyte/macrophage cell lines, U937 and THP-1, detected the expression of the tested molecules while a relatively undifferentiated monocytic cell line, TF-1A, failed to express them. These data indicate that activated and differentiated macrophages are the main cell type expressing tested molecules in atherosclerotic plaques while endothelial and smooth muscle cells can express them in limited cases. Pro-inflammatory activities of the tested molecules may contribute to the atherogenesis by stimulating the cells expressing them in atherosclerotic plaques and the successful treatment of atherosclerosis may require cooperative regulation of these activities.
肿瘤坏死因子超家族(TNFSF)/肿瘤坏死因子受体超家族(TNFRSF)成员参与多种免疫反应和疾病的免疫调节。最近,有报道称LIGHT/TR2、GITRL/GITR和TL1A/DR3在动脉粥样硬化的炎症反应中发挥作用,但尚未对这些分子进行比较分析。为了比较它们的表达模式,我们使用6个人类颈动脉内膜切除术样本进行了免疫组织化学分析。在构成动脉粥样硬化斑块的各种细胞类型中检测到了这些分子的表达。在所有测试样本中,尽管表达水平各不相同,但所有分析分子的表达主要在泡沫巨噬细胞中检测到。在2个和1个斑块样本中,还分别在内皮细胞和平滑肌细胞中检测到了这些分子的强表达,而其他样本仅表达部分测试分子。对人单核细胞/巨噬细胞系U937和THP-1进行的流式细胞术分析检测到了测试分子的表达,而相对未分化的单核细胞系TF-1A未能表达这些分子。这些数据表明,活化和分化的巨噬细胞是动脉粥样硬化斑块中表达测试分子的主要细胞类型,而内皮细胞和平滑肌细胞仅在有限情况下表达这些分子。测试分子的促炎活性可能通过刺激动脉粥样硬化斑块中表达它们的细胞而促进动脉粥样硬化的发生,成功治疗动脉粥样硬化可能需要对这些活性进行协同调节。