Katsuda S, Okada Y, Minamoto T, Oda Y, Matsui Y, Nakanishi I
Department of Pathology, School of Medicine, Kanazawa University, Japan.
Arterioscler Thromb. 1992 Apr;12(4):494-502. doi: 10.1161/01.atv.12.4.494.
This study represents a systematic analysis of the distribution of collagen types in human atherosclerotic lesions. Formalin-fixed, paraffin-embedded aortic tissues of 40 lesions from 16 different individuals ranging in age from 1 month to 84 years were examined immunohistochemically using antibodies to type I, III, IV, V, and VI collagens. Preembedding immunoelectron microscopy was used to simultaneously localize type V and VI collagens within the lesions. Localization of type III collagen was very similar to that of type I, and type VI collagen appeared together with these two types of collagen in the thickened intimas of all stages of the lesion. Type V collagen was not detected in either fatty streaks or the mild intimal thickening of the aortas of children. With advancing age and lesion progression, the immunoreactivity with anti-type V collagen antibody became more intense. Type IV collagen was detected in the basement membrane region of intimal cells. In advanced lesions thick deposits of type IV collagen were found around the elongated smooth muscle cells. Using immunoelectron microscopy, type V collagen was found to be localized to cross-banded collagen fibers, and type VI collagen was found to be localized to beaded filaments present throughout the interstitium of the thickened intima. These findings suggest that collagens preserve the pathophysiological and functional integrity of the vascular wall by providing mechanical support as well as assuring the proper interaction of cells during the formation of atherosclerotic lesions.
本研究对人类动脉粥样硬化病变中胶原蛋白类型的分布进行了系统分析。使用针对I型、III型、IV型、V型和VI型胶原蛋白的抗体,对来自16名年龄从1个月至84岁的不同个体的40个病变的福尔马林固定、石蜡包埋的主动脉组织进行了免疫组织化学检查。采用包埋前免疫电子显微镜技术同时在病变中定位V型和VI型胶原蛋白。III型胶原蛋白的定位与I型非常相似,VI型胶原蛋白与这两种胶原蛋白一起出现在病变各阶段增厚的内膜中。在儿童主动脉的脂肪条纹或轻度内膜增厚中均未检测到V型胶原蛋白。随着年龄的增长和病变进展,抗V型胶原蛋白抗体的免疫反应性变得更强。IV型胶原蛋白在内膜细胞的基底膜区域被检测到。在晚期病变中,在伸长的平滑肌细胞周围发现了大量IV型胶原蛋白沉积。通过免疫电子显微镜观察,发现V型胶原蛋白定位于横纹状胶原纤维,VI型胶原蛋白定位于增厚内膜间质中普遍存在的串珠状细丝。这些发现表明,胶原蛋白通过提供机械支持以及确保动脉粥样硬化病变形成过程中细胞的适当相互作用,维持血管壁的病理生理和功能完整性。