Pasquali-Ronchetti I, Frizziero L, Guerra D, Baccarani-Contri M, Focherini M C, Georgountzos A, Vincenzi D, Cicchetti F, Perbellini A, Govoni E
Institute of General Pathology, University of Modena, Italy.
Semin Arthritis Rheum. 1992 Jun;21(6):400-14. doi: 10.1016/0049-0172(92)90041-b.
Age-associated changes of the human synovium have been investigated by microarthroscopy, optical and electron microscopy, immunohistochemistry, and cytochemistry. The knee joints of nineteen 15- to 56-year-old subjects, classified as normal by inspection, were carefully examined by microarthroscopy; small synovial tissue biopsy specimens from both the suprapatellar pouch and the medial tibiofemoral gutter were taken. Microarthroscopy showed that the villi were more numerous and the vascular network and cell distribution and profiles less regular in aged individuals. These data were confirmed by scanning electron microscopy, which also showed large areas of the synovial surface devoid of cells and collagen bundles in contact with the joint cavity in aged subjects. Light and transmission electron microscopy confirmed these data and allowed evaluation of the number, distribution, shape, and internal organization of cells as well as the distribution of vessels and the organization of the extracellular matrix in the full thickness of the synovium (down to 2 mm). Particular attention was paid to synovial lining cells, among which three main phenotypes could be recognized: synthetic type (present at all ages and hypertrophied in aged subjects), macrophagelike (increasing with age), and fibroblastlike. Collagen increased with age. Further studies are needed for comprehensive understanding of age-associated changes in the human synovium.
通过微关节镜检查、光学显微镜和电子显微镜检查、免疫组织化学以及细胞化学方法,对人类滑膜的年龄相关变化进行了研究。对19名年龄在15至56岁之间、经检查分类为正常的受试者的膝关节进行了仔细的微关节镜检查;从髌上囊和内侧胫股沟采集了小的滑膜组织活检标本。微关节镜检查显示,老年个体的绒毛更多,血管网络以及细胞分布和形态更不规则。扫描电子显微镜证实了这些数据,其还显示老年受试者滑膜表面大片区域无细胞,且与关节腔接触的胶原束减少。光学显微镜和透射电子显微镜证实了这些数据,并能够评估滑膜全层(深至2毫米)中细胞的数量、分布、形状和内部结构,以及血管的分布和细胞外基质的组织。特别关注滑膜衬里细胞,其中可识别出三种主要表型:合成型(在所有年龄段均存在,在老年受试者中肥大)、巨噬细胞样(随年龄增加)和成纤维细胞样。胶原蛋白随年龄增加。需要进一步研究以全面了解人类滑膜的年龄相关变化。