Bauriedel Gerhard, Jabs Alexander, Skowasch Dirk, Hutter Randolph, Badimon Juan J, Fuster Valentin, Welsch Ulrich, Lüderitz Berndt
Department of Medicine-Cardiology, University of Bonn, Sigmund-Freud-Strasse 25, D-53105 Bonn, Germany.
J Am Coll Cardiol. 2003 Sep 3;42(5):930-8. doi: 10.1016/s0735-1097(03)00828-3.
We sought to evaluate: 1) the contribution of dendritic cells (DCs); and 2) the impact of B-cell lymphoma 2 protein (Bcl-2), a central anti-apoptotic protooncogene, and of heat shock protein 47 (HSP47), indicating subsequent collagen deposition, in neointima formation after angioplasty.
The origin of neointimal cells and the factors that promote their accumulation are still unclear. Previous studies reported intimal presence of DCs and suggested cells of primarily extravascular origin to contribute to arterial repair.
Sprague-Dawley rats underwent carotid balloon angioplasty. At different times after angioplasty, tissue sections were analyzed by immunohistochemistry using OX-62 and S100 as DC markers and antibodies against Bcl-2 and HSP47, supplemented by electron microscopic analysis of cell type and apoptosis.
Four days after injury, DCs adhered along the internal elastic lamina and demonstrated intense Bcl-2 and HSP47 expression, consistent with low apoptosis. With ongoing neointima enlargement, luminal DCs remained prevalent and were colocalized with Bcl-2 and HSP47, while signaling decreased to basal regions. Media showed no DCs and only low Bcl-2 and HSP47 immunoreactivity. Adventitia transiently revealed a structural separation between day 4 and 7. Whereas the inner layer demonstrated sparse cellularity, apoptosis and no DC, Bcl-2, and HSP47 labeling, the outer layer was characterized by high myofibroblast density with strong Bcl-2 and HSP47 expression but absence of DCs.
We identify DCs as novel components in early neointima formation, promoted by coordinated anti-apoptotic Bcl-2 and HSP47 expression. Despite intense adventitial remodeling, there is no evidence of adventitial cell transmigration.
我们试图评估:1)树突状细胞(DCs)的作用;2)抗凋亡原癌基因B细胞淋巴瘤2蛋白(Bcl-2)以及提示随后胶原沉积的热休克蛋白47(HSP47)对血管成形术后新生内膜形成的影响。
新生内膜细胞的起源以及促进其积聚的因素仍不清楚。先前的研究报道了DCs在内膜中的存在,并提示主要来自血管外的细胞有助于动脉修复。
对Sprague-Dawley大鼠进行颈动脉球囊血管成形术。在血管成形术后的不同时间,使用OX-62和S100作为DC标志物以及抗Bcl-2和HSP47抗体,通过免疫组织化学分析组织切片,并辅以细胞类型和凋亡的电子显微镜分析。
损伤后4天,DCs沿内弹性膜黏附,并表现出强烈的Bcl-2和HSP47表达,这与低凋亡率一致。随着新生内膜不断扩大,腔内DCs仍然普遍存在,并与Bcl-2和HSP47共定位,而信号传导减少至基底区域。中膜未见DCs,仅显示低水平的Bcl-2和HSP47免疫反应性。外膜在第4天至第7天出现短暂的结构分离。内层细胞稀少、有凋亡现象,且无DC、Bcl-2和HSP47标记,而外层以高肌成纤维细胞密度为特征,Bcl-2和HSP47表达强烈,但无DCs。
我们确定DCs是早期新生内膜形成中的新成分,由抗凋亡的Bcl-2和HSP47协同表达所促进。尽管外膜有强烈的重塑,但没有证据表明外膜细胞发生迁移。