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Effect of cyclic stretching and TGF-beta on the SMAD pathway in fibroblasts

机译:循环拉伸和TGF-β对成纤维细胞SMAD途径的影响

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Tissue engineering requires the response of the cells to different stimuli inducing the synthesis of the extracellular matrix (ECM). It was been shown that mechanical and biochemical stimuli acted on the synthesis of ECM, particularly type I and III collagens. Growth factors implied in transduction pathways are multiple, but the main is TGF-beta. Member of the transforming growth factor-beta (TGF-beta) family bind to type II and type I serine/threonine kinase receptors, which initiate intracellular signals through activation of SMADs proteins. Nevertheless, the effects of mechanical stress of this pathway remain unknown.The aim of this work was to study the pathway of TGF-beta via the SMADs proteins under mechanical (stretching) and biochemical (TGF-beta) stimulations. Endogenous SMADs expression and its modulation by biochemical and mechanical stimulations were evaluated by both flow cytometry and confocal microscopy.Our results demonstrate that 10 ng of TGF-beta and stretching (5%, 1 Hz) applied during 15 min induced a negative feed back loop which blocks the signalling pathway to control TGF-beta activity. This inhibition effect was raised after 1 h of stimulation. Nevertheless, these preliminary studies should be continued by study of expression and localization of inhibitory SMADs (SMAD7).
机译:组织工程需要细胞对不同刺激的反应,诱导细胞外基质(ECM)的合成。结果表明,机械和生化刺激作用于ECM的合成,特别是I型和III型胶原。转导途径中暗示的生长因子是多种,但主要是TGF-β。转化生长因子-β(TGF-β)家族的成员与II型和I型丝氨酸/苏氨酸激酶受体结合,后者通过激活SMADs蛋白启动细胞内信号。然而,该途径的机械应力的影响仍然未知。这项工作的目的是研究在机械(拉伸)和生化(TGF-β)刺激下通过SMADs蛋白的TGF-β途径。通过流式细胞术和共聚焦显微镜评估了内源性SMAD的表达及其在生化和机械刺激下的调节作用。我们的结果表明,在15分钟内施加10 ngTGF-β和拉伸(5%,1 Hz)引起负反馈回路它阻断了控制TGF-beta活性的信号传导途径。刺激1小时后,这种抑制作用增强。但是,这些初步研究应通过研究抑制性SMAD(SMAD7)的表达和定位来继续进行。

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