Schneiderbauer Michaela M, Dutton Charyl M, Scully Sean P
Department of Orthopedics, 200 First Street SW, Mayo Clinic, Rochester, MN 55905, USA.
Cell Signal. 2004 Oct;16(10):1133-40. doi: 10.1016/j.cellsig.2004.03.004.
The objective of this investigation was to clarify how the integrin pathway modulates downstream effectors of the TGF-beta1 pathway in chondrocytic cell signaling. The levels of Smad2 and Smad3 phosphorylation upon TGF-beta1 or alpha2beta1 integrin (Type II collagen) stimulation were analyzed by Western blotting techniques. Cellular response was determined by quantitation of procollagen gene expression. Stimulation of cells with TGF-beta1 and Type II collagen led to rapid phosphorylation of Smad2 and 3 with phosphorylation peaking between 15 min and 1 h. Combined stimulation led to a synergistic increase in the phosphorylation of Smad2 and Smad3. Type II collagen gene expression paralleled Smad phosphorylation. Type II collagen modulates the TGF signaling cascade involving Smad2 and Smad3 leading to an increase in Type II collagen transcription. Therefore, we conclude that TGF-beta1 and integrin stimuli interact prior to Smad2 and 3 phosphorylation in the cytoplasm of chondrocytic cells and regulates the expression of ECM components in chondrocytes.
本研究的目的是阐明整合素途径如何在软骨细胞信号传导中调节TGF-β1途径的下游效应器。通过蛋白质印迹技术分析了TGF-β1或α2β1整合素(II型胶原蛋白)刺激后Smad2和Smad3的磷酸化水平。通过原胶原基因表达定量来确定细胞反应。用TGF-β1和II型胶原蛋白刺激细胞导致Smad2和3迅速磷酸化,磷酸化在15分钟至1小时之间达到峰值。联合刺激导致Smad2和Smad3磷酸化协同增加。II型胶原蛋白基因表达与Smad磷酸化平行。II型胶原蛋白调节涉及Smad2和Smad3的TGF信号级联反应,导致II型胶原蛋白转录增加。因此,我们得出结论,TGF-β1和整合素刺激在软骨细胞胞质中Smad2和3磷酸化之前相互作用,并调节软骨细胞中细胞外基质成分的表达。