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首页> 外文期刊>Cellular Physiology and Biochemistry >Periodic Mechanical Stress Activates Integrinβ1-Dependent Src-Dependent PLCγ1-Independent Rac1 Mitogenic Signal in Rat Chondrocytes through ERK1/2
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Periodic Mechanical Stress Activates Integrinβ1-Dependent Src-Dependent PLCγ1-Independent Rac1 Mitogenic Signal in Rat Chondrocytes through ERK1/2

机译:周期性机械应力通过ERK1 / 2激活大鼠软骨细胞中整合素β1依赖性Src依赖性PLCγ1依赖性Rac1有丝分裂信号。

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The effects of periodic mechanical stress on the mitogenesis of chondrocytes have been studied extensively in recent years. However, the mechanisms underlying the ability of chondrocytes to sense and respond to periodic mechanical stress remain a matter of debate. We explored the signal transduction pathways of proliferation and matrix synthesis when chondrocytes were exposed to periodic mechanical stress. We observed that periodic mechanical stress statistically and significantly enhanced the phosphorylation and activation of Rac1 (ip/i0.05 for each). Pre-treatment with the Rac1 selective inhibitor NSC23766 attenuated periodic mechanical stress-induced chondrocyte proliferation and matrix synthesis (ip/i0.05 for each) and abrogated ERK1/2 signal activation (ip/i0.05), but did not block periodic mechanical stressinduced Src and PLCγ1 phosphorylation in this context. In addition, inhibition of Src with its selective inhibitor PP2 and shRNA targeted to Src blocked Rac1 signal activation (ip/i0.05 for each), but inhibition of the activity of PLCγ1 did not affect the phosphorylation and activation levels of Rac1 under conditions of periodic mechanical stress. The up-regulation of proliferation and matrix synthesis was inhibited in chondrocytes in response to periodic mechanical stress after pretreatment with blocking antibody against integrinβ1 (ip/i0.05 for each) but not after pretreatment with blocking antibody against integrinβ3. The phosphorylation levels of ERK1/2, Rac1, PLCγ1 and Src, and Rac1 activation level were also reduced when integrinβ1 was blocked in this context (ip/i0.05 for each). These findings suggest that periodic mechanical stress promotes chondrocyte proliferation and matrix synthesis in part by activating the ERK1/2 mitogenic signal through the integrinβ1-Src-PLCγ1/Rac1-ERK1/2 pathway, which links these important signaling molecules into mitogenic cascades.
机译:近年来,周期性机械应力对软骨细胞有丝分裂的影响已得到广泛研究。然而,软骨细胞感知和响应周期性机械应力的能力的机制仍存在争议。当软骨细胞暴露于周期性机械应力时,我们探索了增殖和基质合成的信号转导途径。我们观察到,周期性的机械应力在统计学上显着增强了Rac1的磷酸化和激活(每个 p <0.05)。用Rac1选择性抑制剂NSC23766进行的预处理减弱了周期性机械应力诱导的软骨细胞增殖和基质合成(各 p <0.05)并废除了ERK1 / 2信号激活( p <0.05),但在这种情况下并未阻止周期性的机械应力引起的Src和PLCγ1磷酸化。此外,用选择性抑制剂PP2和针对Src的shRNA抑制Src可以阻断Rac1信号激活(每个 p <0.05),但抑制PLCγ1的活性不会影响磷酸化和激活水平Rac1在周期性机械应力条件下的应力。在用抗整合素β1的封闭抗体预处理后,软骨细胞响应周期性的机械应力而抑制了增殖和基质合成的上调(各 p <0.05),但是在用抗整合素β3的封闭抗体预处理后,软骨细胞没有受到周期性机械应力的抑制。当在这种情况下阻断整合素β1时,ERK1 / 2,Rac1,PLCγ1和Src的磷酸化水平以及Rac1激活水平也降低了(每个 p <0.05)。这些发现表明周期性的机械应力部分通过整合素β1-Src-PLCγ1/ Rac1-ERK1 / 2途径激活ERK1 / 2有丝分裂信号来促进软骨细胞增殖和基质合成,该途径将这些重要的信号分子连接到有丝分裂级联反应中。

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