分泌型卷曲相关蛋白3(sFRP3)和 Dickkopf 相关蛋白1(DKK1)根据细胞环境调节成纤维样滑膜细胞标志物和Wnt元件的表达。

sFRP3 and DKK1 Regulate Fibroblast-Like Synoviocytes Markers and Wnt Elements Expression Depending on Cellular Context.

作者信息

Elhaj Mahmoud Dorra, Sassi Nadia, Drissi Ghassen, Barsaoui Maher, Zitouna Khaled, Sahli Hela, Kallel-Sellami Maryam, Kanoun Lassad, Cheour Elhem, Laadhar Lilia

机构信息

a Immuno-Rheumatology Research laboratory, Rheumatology Department , La Rabta Hospital, University of Tunis-El Manar , Tunis , Tunisia.

b Department of Orthopedic Surgery and Traumatology , La Rabta Hospital , Tunis , Tunisia.

出版信息

Immunol Invest. 2017 Apr;46(3):314-328. doi: 10.1080/08820139.2016.1267204. Epub 2017 Feb 2.

Abstract

CONTEXT

Fibroblast-like synoviocytes (FLS) from rheumatoid arthritis (RA) display pathogenic behavior. Various members of the Wnt pathway, especially the canonical Wnt/β-catenin cascade, may contribute to autonomous RA FLS activation. It has been shown that the two Wnt inhibitors: sFRP3 and DKK1 contribute to several critical aspects of joint biology. However, their effects on RA FLS are poorly characterized. The aim of our study was to investigate the effects of sFRP3 and DKK1 on FLS markers, Wnt components, and target oncogenes expression by RA FLS and compare the findings to osteoarthritic (OA) FLS.

MATERIALS AND METHODS

RA and OA FLS were treated with sFRP3 and DKK1 for 6 days. Wnt signaling components (Wnt5a, LRP5 and β-catenin), Wnt target oncogenes (cyclin E1 and WISP1), and FLS markers (fibronectin and MMP3) were analyzed using western blotting and/or qRT-PCR.

RESULTS

Our data indicated that sFRP3 down-regulated the key gene β-catenin in RA FLS. sFRP3 decreased fibronectin, a well-known downstream effectors gene of Wnt/β-catenin pathway, and LRP5 expression in both RA and OA FLS. In OA FLS, sFRP3 induced increased expression of Wnt5a and MMP3 but did not affect their levels in RA FLS. On the other hand, DKK1 increased fibronectin expression in RA FLS and decreased its expression in OA FLS.

CONCLUSION

Our results confirm the involvement of Wnt signaling in FLS transformation and show that two inhibitors of the same cascade can regulate differently the same elements and that a single inhibitor can initiate signaling depending on cellular context.

ABBREVIATIONS

FLS: fibroblast-like synoviocytes; RA: rheumatoid arthritis; Wnt: Wingless; Fz: frizzled; LRP: Fz/low-density lipoprotein receptor protein; WISP1: Wnt1 inducible signaling pathway protein 1; sFRP: secreted Fz-related proteins; DKK: Dickkopf; OA: osteoarthritis; DMEM: Dulbecco's modified Eagle's medium; FBS: fetal bovine serum; PBS: phosphate buffered saline; SDS-PAGE: sodium dodecyl sulfate-polyacrylamide gel electrophoresis; ECL: enhanced chemiluminescence detection solution; MMP3: metaloproteinase 3; qRT-PCR: quantitative real-time polymerase chain reaction; S.D: standard deviation; CRD: cysteine-rich domain; MeCP2: methyl-CpG-binding protein; RANKL: nuclear factor-kappa B ligand.

摘要

背景

类风湿关节炎(RA)患者的成纤维样滑膜细胞(FLS)表现出致病行为。Wnt信号通路的各种成员,尤其是经典的Wnt/β-连环蛋白级联反应,可能导致RA FLS自主激活。研究表明,两种Wnt抑制剂:分泌型卷曲相关蛋白3(sFRP3)和Dickkopf-1(DKK1)在关节生物学的几个关键方面发挥作用。然而,它们对RA FLS的影响尚不清楚。本研究旨在探讨sFRP3和DKK1对RA FLS的FLS标志物、Wnt信号成分及靶癌基因表达的影响,并将结果与骨关节炎(OA)FLS进行比较。

材料与方法

用sFRP3和DKK1处理RA和OA FLS 6天。使用蛋白质免疫印迹法和/或定量逆转录聚合酶链反应(qRT-PCR)分析Wnt信号成分(Wnt5a、低密度脂蛋白受体相关蛋白5(LRP5)和β-连环蛋白)、Wnt靶癌基因(细胞周期蛋白E1和Wnt1诱导信号通路蛋白1(WISP1))以及FLS标志物(纤连蛋白和基质金属蛋白酶3(MMP3))。

结果

我们的数据表明,sFRP3下调了RA FLS中的关键基因β-连环蛋白。sFRP3降低了纤连蛋白(Wnt/β-连环蛋白信号通路的一个众所周知的下游效应基因)以及RA和OA FLS中LRP5的表达。在OA FLS中,sFRP3诱导Wnt5a和MMP3表达增加,但对RA FLS中的这些水平没有影响。另一方面,DKK1增加了RA FLS中纤连蛋白的表达,而降低了OA FLS中纤连蛋白的表达。

结论

我们的结果证实了Wnt信号参与FLS转化,并表明同一级联反应的两种抑制剂可以对相同的元件产生不同的调节作用,而且单一抑制剂可根据细胞环境启动信号传导。

缩写

FLS:成纤维样滑膜细胞;RA:类风湿关节炎;Wnt:无翅型;Fz:卷曲蛋白;LRP:Fz/低密度脂蛋白受体相关蛋白;WISP1:Wnt1诱导信号通路蛋白1;sFRP:分泌型卷曲相关蛋白;DKK:Dickkopf蛋白;OA:骨关节炎;DMEM:杜氏改良伊格尔培养基;FBS:胎牛血清;PBS:磷酸盐缓冲液;SDS-PAGE:十二烷基硫酸钠-聚丙烯酰胺凝胶电泳;ECL:增强化学发光检测溶液;MMP3:基质金属蛋白酶3;qRT-PCR:定量实时聚合酶链反应;S.D:标准差;CRD:富含半胱氨酸结构域;MeCP2:甲基化CpG结合蛋白;RANKL:核因子κB配体

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