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瘦素增强人骨关节炎软骨中 MMP-1、MMP-3 和 MMP-13 的产生,并与 OA 患者滑液中的 MMP-1 和 MMP-3 相关。

Leptin enhances MMP-1, MMP-3 and MMP-13 production in human osteoarthritic cartilage and correlates with MMP-1 and MMP-3 in synovial fluid from OA patients.

机构信息

The Immunopharmacology Research Group, Tampere University Hospital, Tampere, Finland.

出版信息

Clin Exp Rheumatol. 2011 Jan-Feb;29(1):57-64. Epub 2011 Feb 23.

Abstract

OBJECTIVES

In the present study, we investigated the role of adipocytokine leptin in the pathogenesis of osteoarthritis (OA) by measuring its effects on matrix metalloproteinase (MMP) production in human OA cartilage. In addition, the correlations between leptin and MMP concentrations in synovial fluid from OA patients were studied.

METHODS

Cartilage tissue obtained from leftover pieces of total knee replacement surgery from patients with OA was used in the experiments. Production of collagenases MMP-1, MMP-8 and MMP-13, and stromelysin-1 (MMP-3) in the cartilage was measured by immunoassay and the signalling pathways were explored by pharmacological means. In addition, synovial fluid samples were collected from 84 OA patients undergoing knee replacement surgery. The concentrations of leptin and MMPs in synovial fluid were measured by immunoassay.

RESULTS

Leptin alone and in combination with IL-1β enhanced production of MMP-1, MMP-3, and MMP-13 in human OA cartilage, while MMP-8 concentrations remained undetectable. The effects of leptin on MMP-1, MMP-3 and MMP-13 production were mediated through transcription factor NF-κβ, and through protein kinase C and MAP kinase pathways. Interestingly, leptin concentrations in synovial fluid from OA patients correlated positively with MMP-3 (r=0.51, p<0.001) and MMP-1 (r=0.41, p<0.001) levels.

CONCLUSIONS

To our knowledge, this is the first study to show that leptin up-regulates MMP-1 and MMP-3 production in human OA cartilage and correlates positively to MMP-1 and MMP-3 in synovial fluid from OA patients. The findings suggest that leptin has catabolic effects in OA joints by increasing MMP production in cartilage.

摘要

目的

在本研究中,我们通过测量瘦素对人骨关节炎(OA)软骨中基质金属蛋白酶(MMP)产生的影响,研究了脂肪细胞因子瘦素在 OA 发病机制中的作用。此外,还研究了 OA 患者滑液中瘦素与 MMP 浓度之间的相关性。

方法

实验中使用了来自 OA 患者全膝关节置换术剩余部分的软骨组织。通过免疫测定法测量软骨中胶原酶 MMP-1、MMP-8 和 MMP-13 以及基质金属蛋白酶-3(MMP-3)的产生,并通过药理学方法探索信号通路。此外,还从 84 名接受膝关节置换术的 OA 患者中采集滑液样本。通过免疫测定法测量滑液中瘦素和 MMP 的浓度。

结果

瘦素单独或与 IL-1β 联合增强了人 OA 软骨中 MMP-1、MMP-3 和 MMP-13 的产生,而 MMP-8 浓度仍无法检测到。瘦素对 MMP-1、MMP-3 和 MMP-13 产生的影响是通过转录因子 NF-κβ 以及蛋白激酶 C 和 MAP 激酶途径介导的。有趣的是,OA 患者滑液中的瘦素浓度与 MMP-3(r=0.51,p<0.001)和 MMP-1(r=0.41,p<0.001)水平呈正相关。

结论

据我们所知,这是第一项表明瘦素上调人 OA 软骨中 MMP-1 和 MMP-3 产生并与 OA 患者滑液中 MMP-1 和 MMP-3 呈正相关的研究。这些发现表明,瘦素通过增加软骨中 MMP 的产生对 OA 关节具有分解代谢作用。

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