Fleischmajer R, Gay S, Meigel W N, Perlish J S
Arthritis Rheum. 1978 May;21(4):418-28. doi: 10.1002/art.1780210404.
The collagen in localized and systemic scleroderma skin was studied by light microscopy with silver impregnation (50 patients), electron microscopy (14 patients), and immunofluorescence microscopy using specific antibodies against Type I and Type III collagens (12 patients). In the cellular stage, the dermis and adipose tissue revealed perivascular or diffuse cellular infiltrates (mostly lymphocytes, plasma cells, and macrophages), accompanied by deposition of Type III collagen. The lower dermis also showed an increase in Type III collagen. In the fibrotic stage, the papillary layer showed a reduction and/or clumping of Type III collagen as compared to normal skin. The lower dermis and the adipose tissue revealed compact collagen consisting exclusively of Type I collagen or a mixture of Type I and Type III collagen. The pattern of Type III collagen distribution was similar to that of reticulin, thus suggesting that at least some reticulin fibrils may represent Type III collagen.
通过银浸染的光学显微镜(50例患者)、电子显微镜(14例患者)以及使用抗I型和III型胶原特异性抗体的免疫荧光显微镜(12例患者)对局限性和系统性硬皮病皮肤中的胶原进行了研究。在细胞期,真皮和脂肪组织显示血管周围或弥漫性细胞浸润(主要为淋巴细胞、浆细胞和巨噬细胞),伴有III型胶原沉积。真皮下部也显示III型胶原增加。在纤维化期,与正常皮肤相比,乳头层显示III型胶原减少和/或聚集。真皮下部和脂肪组织显示紧密的胶原,仅由I型胶原或I型和III型胶原混合物组成。III型胶原的分布模式与网硬蛋白相似,因此表明至少一些网硬蛋白纤维可能代表III型胶原。