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通过原位杂交对类风湿性关节炎和骨关节炎患者滑膜组织中组织蛋白酶L、组织蛋白酶D和胶原酶信使核糖核酸表达的比较分析。

Comparative analysis of cathepsin L, cathepsin D, and collagenase messenger RNA expression in synovial tissues of patients with rheumatoid arthritis and osteoarthritis, by in situ hybridization.

作者信息

Keyszer G M, Heer A H, Kriegsmann J, Geiler T, Trabandt A, Keysser M, Gay R E, Gay S

机构信息

University of Alabama, Department of Medicine, Birmingham 35294-0006, USA.

出版信息

Arthritis Rheum. 1995 Jul;38(7):976-84. doi: 10.1002/art.1780380714.

Abstract

OBJECTIVE

To compare the expression of cathepsin L, cathepsin D, and collagenase messenger RNA (mRNA) in synovial specimens from patients with rheumatoid arthritis (RA) and osteoarthritis (OA).

METHODS

The expression of cathepsins L and D as well as collagenase mRNA in synovial tissues from 8 patients with RA, 6 patients with OA, and 2 patients with noninflamed joints was evaluated using in situ hybridization with digoxigenin-labeled RNA probes.

RESULTS

Both RA and OA synovial tissue expressed cathepsins L and D as well as collagenase mRNA. The expression of the cathepsins was markedly higher in interstitial regions and, to some extent, in perivascular infiltrates of RA synovial tissue compared with OA specimens.

CONCLUSION

Cathepsins L and D mRNA are expressed differently in RA and OA synovial tissues, supporting the concept that these enzymes may contribute to the influx of mononuclear cells into RA synovium. Moreover, the data reveal that the expression of collagenase and cathepsins in RA and OA synovial lining is otherwise largely similar, and suggest that the adhesion of synovial cells to cartilage mediates the invasive destructive process in RA.

摘要

目的

比较类风湿关节炎(RA)和骨关节炎(OA)患者滑膜标本中组织蛋白酶L、组织蛋白酶D和胶原酶信使核糖核酸(mRNA)的表达情况。

方法

使用地高辛标记的RNA探针进行原位杂交,评估8例RA患者、6例OA患者和2例非炎症关节患者滑膜组织中组织蛋白酶L和D以及胶原酶mRNA的表达。

结果

RA和OA滑膜组织均表达组织蛋白酶L和D以及胶原酶mRNA。与OA标本相比,RA滑膜组织间质区域以及在一定程度上血管周围浸润中组织蛋白酶的表达明显更高。

结论

组织蛋白酶L和D mRNA在RA和OA滑膜组织中的表达不同,支持了这些酶可能促使单核细胞流入RA滑膜的观点。此外,数据显示RA和OA滑膜衬里中胶原酶和组织蛋白酶的表达在其他方面基本相似,并表明滑膜细胞与软骨的粘附介导了RA中的侵袭性破坏过程。

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