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人膝关节晚期骨关节炎软骨细胞的基因表达在纤维样和完整软骨中均发生改变,而无普遍软骨细胞肥大的证据。

Gene expression in human chondrocytes in late osteoarthritis is changed in both fibrillated and intact cartilage without evidence of generalised chondrocyte hypertrophy.

机构信息

Wellcome Trust Centre for Cell-Matrix Research, University of Manchester, Manchester, UK.

出版信息

Ann Rheum Dis. 2010 Jan;69(1):234-40. doi: 10.1136/ard.2008.097139.

Abstract

OBJECTIVES

To investigate changes in gene expression in fibrillated and intact human osteoarthritis (OA) cartilage for evidence of an altered chondrocyte phenotype and hypertrophy.

METHODS

Paired osteochondral samples were taken from a high-load site and a low-load site from 25 OA joints and were compared with eight similar paired samples from age-matched controls. Gene expression of key matrix and regulatory genes was analysed by quantitative real-time reverse transcription-polymerase chain reaction on total RNA extracted from the cartilage.

RESULTS

There was a major change in chondrocyte gene expression in OA cartilage. SOX9 (38-fold) and aggrecan (4-fold) gene expression were both lower in OA (p<0.001), and collagen I (17-fold) and II (2.5-fold) gene expression were each increased in a subset of OA samples. The major changes in gene expression were similar at the fibrillated high-loaded site and the intact low-loaded site. There was no evidence of a generalised change in OA to proliferative or hypertrophic phenotype as seen in the growth plate, as genes associated with either stage of differentiation were unchanged (PTHrPR), or significantly downregulated (collagen X (14-fold, p<0.002), VEGF (23-fold, p<0.02), BCL-2 (5.6-fold, p<0.001), matrilin-1 (6.5-fold, p<0.001)). In contrast MMP-13 was significantly upregulated in the OA cartilage samples (5.3-fold, p<0.003).

CONCLUSIONS

The expression of key chondrocyte genes, including aggrecan and SOX9, was decreased in OA cartilage and the changes were similar in both fibrillated high-loaded and intact low-loaded cartilage on the same joint. However, there was no significant upregulation of type X collagen, and other genes associated with chondrocyte further differentiation and hypertrophy.

摘要

目的

研究纤维性和完整的人骨关节炎(OA)软骨中的基因表达变化,以寻找软骨细胞表型和肥大改变的证据。

方法

从 25 个 OA 关节的高负荷部位和低负荷部位采集配对的骨软骨样本,并与 8 个年龄匹配的对照的类似配对样本进行比较。从软骨中提取的总 RNA 上,通过定量实时逆转录聚合酶链反应分析关键基质和调节基因的表达。

结果

OA 软骨中软骨细胞基因表达发生了重大变化。SOX9(38 倍)和聚集蛋白聚糖(4 倍)的基因表达均降低(p<0.001),而胶原 I(17 倍)和 II(2.5 倍)的基因表达在一部分 OA 样本中增加。在纤维性高负荷部位和完整的低负荷部位,基因表达的主要变化相似。OA 中未见向增殖或肥大表型的一般变化,如与分化的任一阶段相关的基因不变(PTHrPR),或明显下调(X 型胶原(14 倍,p<0.002),VEGF(23 倍,p<0.02),BCL-2(5.6 倍,p<0.001),基质金属蛋白酶-13(MMP-13)(5.3 倍,p<0.003)。

结论

OA 软骨中关键软骨细胞基因的表达,包括聚集蛋白聚糖和 SOX9,降低了,并且在同一关节的纤维性高负荷和完整的低负荷软骨中变化相似。然而,没有明显的 X 型胶原和其他与软骨细胞进一步分化和肥大相关的基因的上调。

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