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基质糖胺聚糖的改变会削弱关节软骨细胞对经典Wnt信号的反应。

Alteration of matrix glycosaminoglycans diminishes articular chondrocytes' response to a canonical Wnt signal.

作者信息

Shortkroff S, Yates K E

机构信息

Department of Orthopedic Surgery, Brigham and Women's Hospital and Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.

出版信息

Osteoarthritis Cartilage. 2007 Feb;15(2):147-54. doi: 10.1016/j.joca.2006.07.004. Epub 2006 Sep 5.

Abstract

OBJECTIVE

Although Wnt signaling is a key regulator of the chondrocyte life cycle during embryonic development, little is known about Wnt activity in articular cartilage. Recent studies have suggested an association between excess signaling through the canonical Wnt pathway and osteoarthritis (OA). Genetic and in vitro studies with Drosophila have shown that signaling by the orthologous protein, Wingless (Wg), is regulated by glycosaminoglycans (GAGs) found at the cell surface. The objective of this study was to determine whether alteration in GAG sulfation or matrix content, such as that occurs in OA cartilage, would affect articular chondrocytes' response to a canonical Wnt stimulus.

METHODS

Cells were isolated from shoulder joints of young calves (bovine articular chondrocytes, bACs) and from human cartilage (human articular chondrocytes, hACs) discarded during total knee replacement for OA. Conditioned media from a cell line that is stably transfected with Wnt3a was used as a source of Wnt protein that activates the canonical signaling pathway. Conditioned media from the parental cell line was used as a control. beta-catenin levels were measured by immunoblot. In some experiments, chondrocyte cultures were treated with sodium chlorate (NaClO3) to inhibit GAG sulfation, or with chondroitinase ABC (ChABC) to digest chondroitin sulfate (CS) in the matrix.

RESULTS

Cultured bACs showed low steady-state levels of beta-catenin that increased upon stimulation with Wnt3a. A decrease in either GAG sulfation or CS content diminished bACs' response to Wnt3a (approximately 40% and 37% of control, respectively). Similar effects on the response to Wnt3a via beta-catenin were observed for cultured hACs with undersulfation of GAGs (16% of control) and decreased CS content (20% of control).

CONCLUSION

This study demonstrates that articular chondrocytes respond to canonical Wnt stimulation, and that reduced sulfation or CS content diminishes that response.

摘要

目的

尽管Wnt信号通路是胚胎发育过程中软骨细胞生命周期的关键调节因子,但关于关节软骨中的Wnt活性却知之甚少。最近的研究表明,经典Wnt通路的过度信号传导与骨关节炎(OA)之间存在关联。对果蝇的遗传学和体外研究表明,同源蛋白无翅(Wg)的信号传导受细胞表面发现的糖胺聚糖(GAG)调节。本研究的目的是确定GAG硫酸化或基质含量的改变(如OA软骨中发生的那样)是否会影响关节软骨细胞对经典Wnt刺激的反应。

方法

从幼年小牛的肩关节分离细胞(牛关节软骨细胞,bACs)以及从因OA行全膝关节置换术中丢弃的人软骨中分离细胞(人关节软骨细胞,hACs)。用稳定转染Wnt3a的细胞系的条件培养基作为激活经典信号通路的Wnt蛋白来源。亲本细胞系的条件培养基用作对照。通过免疫印迹法测量β-连环蛋白水平。在一些实验中,软骨细胞培养物用氯酸钠(NaClO3)处理以抑制GAG硫酸化,或用软骨素酶ABC(ChABC)处理以消化基质中的硫酸软骨素(CS)。

结果

培养的bACs显示β-连环蛋白的稳态水平较低,在用Wnt3a刺激后升高。GAG硫酸化或CS含量的降低均减弱了bACs对Wnt3a的反应(分别约为对照的40%和37%)。对于GAG硫酸化不足(为对照的16%)和CS含量降低(为对照的20%)的培养hACs,观察到对通过β-连环蛋白对Wnt3a反应的类似影响。

结论

本研究表明关节软骨细胞对经典Wnt刺激有反应,并且硫酸化减少或CS含量降低会减弱这种反应。

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