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脂联素与人类骨关节炎中软骨降解之间的关联。

Association between adiponectin and cartilage degradation in human osteoarthritis.

作者信息

Francin P-J, Abot A, Guillaume C, Moulin D, Bianchi A, Gegout-Pottie P, Jouzeau J-Y, Mainard D, Presle N

机构信息

UMR 7365 CNRS-Universite de Lorraine, Biopôle de l'Universite de Lorraine, campus Biologie-Sante, Avenue de la forêt de Haye, BP 184, 54505 Vandoeuvre-les-Nancy, France.

出版信息

Osteoarthritis Cartilage. 2014 Mar;22(3):519-26. doi: 10.1016/j.joca.2014.01.002. Epub 2014 Jan 24.

Abstract

OBJECTIVE

Conflicting findings raise questions about the role of adiponectin in osteoarthritis (OA). The current study aimed to investigate in OA patients the association between the production of adiponectin and the grade of cartilage destruction, and to provide functional evidence for a potential role of adiponectin in OA.

DESIGN

The expression of adiponectin was examined by immunohistochemistry in cartilage obtained from healthy individuals (n = 2; ages 56 and 41 years; 1 male and 1 female) and OA patients (n = 11; ages 64-79 years; 2 male and 9 female). The association between its production in chondrocytes and the grade of cartilage destruction was established on full-depth cartilage biopsies. The functional activity of adiponectin in OA cartilage was determined from the relation between the expression of adiponectin, its receptor, cartilage-specific components and factors involved in matrix degradation, and from the chondrocyte response to the full-length or the globular form of adiponectin.

RESULTS

Adiponectin was not detected in healthy cartilage. Conversely, the adipokine was up-regulated in damaged tissue, but no strong association with the grade of cartilage destruction was found. We showed a positive correlation between adiponectin and mPGES or MMP-13 while AdipoR1 was related to the expression of type 2 collagen, aggrecan and Sox9. The full-length form of adiponectin but not the globular isoform, stimulated the production of PGE2 and MMP-13 activity in cultured human chondrocytes.

CONCLUSIONS

The elevated level of adiponectin found in chondrocytes from OA patients might contribute to matrix remodelling during OA, the full-length isoform being the single active form.

摘要

目的

相互矛盾的研究结果引发了关于脂联素在骨关节炎(OA)中作用的疑问。本研究旨在调查OA患者中脂联素产生与软骨破坏程度之间的关联,并为脂联素在OA中的潜在作用提供功能证据。

设计

通过免疫组织化学检测从健康个体(n = 2;年龄分别为56岁和41岁;1男1女)和OA患者(n = 11;年龄64 - 79岁;2男9女)获取的软骨中脂联素的表达。在全层软骨活检中确定其在软骨细胞中的产生与软骨破坏程度之间的关联。根据脂联素及其受体的表达、软骨特异性成分和参与基质降解的因子之间的关系,以及软骨细胞对全长或球状形式脂联素的反应,确定脂联素在OA软骨中的功能活性。

结果

在健康软骨中未检测到脂联素。相反,该脂肪因子在受损组织中上调,但未发现与软骨破坏程度有强关联。我们发现脂联素与mPGES或MMP - 13呈正相关,而AdipoR1与Ⅱ型胶原蛋白、聚集蛋白聚糖和Sox9的表达相关。全长形式的脂联素而非球状异构体,刺激培养的人软骨细胞中PGE2的产生和MMP - 13活性。

结论

OA患者软骨细胞中发现的脂联素水平升高可能有助于OA期间的基质重塑,全长异构体是唯一的活性形式。

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