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骨关节炎患者膝关节软骨中软骨细胞的基质金属蛋白酶1、3和9的基因表达具有区域和分级特异性。

Gene expression of matrix metalloproteinases 1, 3, and 9 by chondrocytes in osteoarthritic human knee articular cartilage is zone and grade specific.

作者信息

Freemont A J, Hampson V, Tilman R, Goupille P, Taiwo Y, Hoyland J A

机构信息

Department of Pathological Science, University of Manchester.

出版信息

Ann Rheum Dis. 1997 Sep;56(9):542-9. doi: 10.1136/ard.56.9.542.

Abstract

OBJECTIVES

Matrix metalloproteinases (MMPs) are thought to be major mediators of cartilage destruction. Osteoarthritis (OA) is characterised by cartilage degradation. This study explores gene expression of three MMPs in articular chondrocytes during the histological development of the cartilage lesion of OA.

METHODS

Biopsy specimens of human normal and OA cartilage, classified into four grades on the basis of histology, were probed for MMPs 1, 3, and 9 using 35S-labelled cDNA probes. The signal was measured at four different depths (zones) using an automated image analyser and compared with signal from sections probed with lambda DNA. Rheumatoid synovium was used as a positive control for MMP gene expression.

RESULTS

Rheumatoid tissue contained mRNA for all three MMPs. Expression in chondrocytes varied with the depth of the chondrocyte in the cartilage and the histomorphological extent of the OA changes. There was no detectable mRNA signal for these three MMPs in normal cartilage. In general, in OA, MMP-1 gene expression was greatest in the superficial cartilage in established disease. By contrast mRNAs for MMP-3 and 9 were expressed deeper in the cartilage, MMP-9 early in disease and MMP-3 with a biphasic pattern in early and late stage disease, most pronounced in the latter. This was a consequence of differential expression in single cells and chondrocyte clusters in late disease.

CONCLUSION

The data indicate that expression of genes for MMPs 1, 3, and 9 is differentially regulated in human articular chondrocytes and, in individual cells, is related to the depth of the chondrocyte below the cartilage surface and the nature and extent of the cartilage lesion.

摘要

目的

基质金属蛋白酶(MMPs)被认为是软骨破坏的主要介质。骨关节炎(OA)的特征是软骨退化。本研究探讨在OA软骨病变组织学发展过程中,三种MMPs在关节软骨细胞中的基因表达。

方法

根据组织学将人正常和OA软骨活检标本分为四个等级,使用35S标记的cDNA探针检测MMPs 1、3和9。使用自动图像分析仪在四个不同深度(区域)测量信号,并与用λDNA探针检测的切片信号进行比较。类风湿滑膜用作MMP基因表达的阳性对照。

结果

类风湿组织含有所有三种MMPs的mRNA。软骨细胞中的表达随软骨中软骨细胞的深度以及OA变化的组织形态学程度而变化。在正常软骨中未检测到这三种MMPs的mRNA信号。一般来说,在OA中,MMP-1基因表达在已确诊疾病的表层软骨中最高。相比之下,MMP-3和9的mRNA在软骨中表达更深,MMP-9在疾病早期表达,MMP-3在疾病早期和晚期呈双相模式表达,在晚期最为明显。这是晚期疾病中单个细胞和软骨细胞簇中差异表达的结果。

结论

数据表明,MMPs 1、3和9的基因表达在人关节软骨细胞中受到差异调节,并且在单个细胞中,与软骨表面以下软骨细胞的深度以及软骨病变的性质和程度有关。

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2
Metalloproteinases in the rheumatic diseases.风湿性疾病中的金属蛋白酶。
J Pathol. 1996 Oct;180(2):115-7. doi: 10.1002/(SICI)1096-9896(199610)180:2<115::AID-PATH674>3.0.CO;2-I.

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