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关节软骨浅层中外源性激活的 TGF-β的积累。

Accumulation of exogenous activated TGF-β in the superficial zone of articular cartilage.

机构信息

Department of Mechanical Engineering, Columbia University, New York, New York, USA.

出版信息

Biophys J. 2013 Apr 16;104(8):1794-804. doi: 10.1016/j.bpj.2013.02.052.

Abstract

It was recently demonstrated that mechanical shearing of synovial fluid (SF), induced during joint motion, rapidly activates latent transforming growth factor β (TGF-β). This discovery raised the possibility of a physiological process consisting of latent TGF-β supply to SF, activation via shearing, and transport of TGF-β into the cartilage matrix. Therefore, the two primary objectives of this investigation were to characterize the secretion rate of latent TGF-β into SF, and the transport of active TGF-β across the articular surface and into the cartilage layer. Experiments on tissue explants demonstrate that high levels of latent TGF-β1 are secreted from both the synovium and all three articular cartilage zones (superficial, middle, and deep), suggesting that these tissues are capable of continuously replenishing latent TGF-β to SF. Furthermore, upon exposure of cartilage to active TGF-β1, the peptide accumulates in the superficial zone (SZ) due to the presence of an overwhelming concentration of nonspecific TGF-β binding sites in the extracellular matrix. Although this response leads to high levels of active TGF-β in the SZ, the active peptide is unable to penetrate deeper into the middle and deep zones of cartilage. These results provide strong evidence for a sequential physiologic mechanism through which SZ chondrocytes gain access to active TGF-β: the synovium and articular cartilage secrete latent TGF-β into the SF and, upon activation, TGF-β transports back into the cartilage layer, binding exclusively to the SZ.

摘要

最近有人证明,关节运动时产生的滑膜液(SF)的机械剪切作用能迅速激活潜伏的转化生长因子β(TGF-β)。这一发现使人们联想到一种生理过程,即潜伏的 TGF-β源源不断地供应给 SF,经剪切作用激活后,再转运到软骨基质中。因此,本研究的两个主要目标是确定潜伏 TGF-β分泌到 SF 中的分泌速率,以及 TGF-β穿过关节表面并进入软骨层的转运速率。组织标本实验表明,滑膜和所有三个关节软骨区(浅层、中层和深层)都能大量分泌潜伏 TGF-β1,表明这些组织有能力持续向 SF 补充潜伏 TGF-β。此外,当软骨暴露于活性 TGF-β1 时,由于细胞外基质中存在大量非特异性 TGF-β 结合位点,该肽在浅层区(SZ)蓄积。尽管这种反应导致 SZ 中 TGF-β 的活性水平很高,但活性肽无法穿透软骨的中层和深层。这些结果为一个连续的生理机制提供了有力的证据,通过该机制,SZ 软骨细胞可以获得活性 TGF-β:滑膜和关节软骨将潜伏 TGF-β分泌到 SF 中,经激活后,TGF-β又转运回软骨层,仅与 SZ 结合。

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