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实验性变应性关节炎中滑膜衬里的细胞分裂:慢性关节炎发展过程中细胞的增殖

Cell division in the synovial lining in experimental allergic arthritis: proliferation of cells during the development of chronic arthritis.

作者信息

Henderson B, Glynn L E, Chayen J

出版信息

Ann Rheum Dis. 1982 Jun;41(3):275-81. doi: 10.1136/ard.41.3.275.

Abstract

The synovial tissue in experimentally induced immune arthritis induced in the rabbit has been used as a model of rheumatoid arthritis to determine which cells may contribute to the growth of this tissue. Tissue from the challenged and from the unchallenged knee joints was taken, after the intra-articular injection of a small amount of tritiated thymidine, from rabbits up to 3 months after the arthritis was induced. DNA synthesis, as a measure of cell proliferative activity, was assessed firstly by measuring the labelling index in autoradiographs of sections of such tissue, and secondly by the DNA synthetic index obtained by Feulgen cytophotometry. These measurements were made separately on synoviocytes, on the structural cells of the stroma, on the cells lining the small blood vessels, and on the infiltrating inflammatory cells. The DNA synthetic activity of the synoviocytes, and of the stromal noninflammatory cells, was maximal between 3 and 7 days after challenge. The activity in the synoviocytes, in particular, remained raised for up to 84 days after the challenge. Thus these cells appear to be capable of contributing to the hyperplasia, but the contribution of other cells, deeper in the stroma, cannot be excluded.

摘要

兔实验性诱导免疫性关节炎中的滑膜组织已被用作类风湿性关节炎的模型,以确定哪些细胞可能有助于该组织的生长。在关节内注射少量氚标记的胸腺嘧啶核苷后,从诱发关节炎后长达3个月的兔子身上获取受攻击和未受攻击膝关节的组织。作为细胞增殖活性的一种衡量指标,DNA合成首先通过测量此类组织切片放射自显影片中的标记指数来评估,其次通过福尔根细胞光度法获得的DNA合成指数来评估。这些测量分别在滑膜细胞、基质结构细胞、小血管内衬细胞和浸润性炎症细胞上进行。滑膜细胞和基质非炎症细胞的DNA合成活性在攻击后3至7天达到最大值。特别是滑膜细胞的活性在攻击后长达84天仍保持升高。因此,这些细胞似乎能够导致增生,但不能排除基质中更深层其他细胞的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1423/1000927/35750d0d2979/annrheumd00110-0074-a.jpg

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