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首页> 外文期刊>American Journal of Translational Research >The MEK-ERK1/2 signaling pathway regulates hyaline cartilage formation and the redifferentiation of dedifferentiated chondrocytes in vitro
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The MEK-ERK1/2 signaling pathway regulates hyaline cartilage formation and the redifferentiation of dedifferentiated chondrocytes in vitro

机译:MEK-ERK1 / 2信号通路在体外调节透明软骨的形成和去分化软骨细胞的再分化

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摘要

The aim of this study was to investigate the role of the mitogen-activated protein kinase kinase-extracellular signal-regulated kinases 1/2 (MEK-ERK1/2) signaling pathway in chondrocyte differentiation and cartilage tissue construction in vitro. Chondrocytes were stimulated with rat serum (RS) and fetal bovine serum (FBS), and chondrocyte phenotypes were investigated microscopically. Chondrocyte proliferation was analyzed using fluorescence activated cell sorting (FACS) and the CCK8 method. Protein and mRNA expressions were assessed by western blot and RT-qPCR. Constructed cartilage tissues were examined by Safranin O-Fast Green FCF staining and immunofluorescence. In contrast to FBS, RS induced rapid dedifferentiation of chondrocytes and decreased type II collagen expression and proteoglycan synthesis. ERK1/2 and type I collagen expression increased during dedifferentiation and decreased during redifferentiation. Increased MEK-ERK1/2 pathway activity resulted in chondrocyte dedifferentiation, and inhibition of ERK1/2 by the inhibitor PD0325901 reversed dedifferentiation and led to redifferentiation. These data suggest strongly that inhibition of MEK-ERK1/2 activation prevents chondrocyte dedifferentiation and fibrocartilage formation.
机译:这项研究的目的是调查有丝分裂原激活的蛋白激酶激酶-细胞外信号调节激酶1/2(MEK-ERK1 / 2)信号通路在体外软骨细胞分化和软骨组织构建中的作用。用大鼠血清(RS)和胎牛血清(FBS)刺激软骨细胞,并在显微镜下研究软骨细胞的表型。使用荧光激活细胞分选(FACS)和CCK8方法分析软骨细胞的增殖。通过蛋白质印迹和RT-qPCR评估蛋白质和mRNA表达。通过番红O型快速绿色FCF染色和免疫荧光检查构建的软骨组织。与FBS相比,RS诱导软骨细胞快速去分化并降低II型胶原蛋白表达和蛋白聚糖合成。 ERK1 / 2和I型胶原蛋白表达在去分化过程中增加,而在再分化过程中则下降。 MEK-ERK1 / 2途径活性的增加导致软骨细胞去分化,并且抑制剂PD0325901对ERK1 / 2的抑制使去分化逆转并导致了再分化。这些数据强烈表明,抑制MEK-ERK1 / 2激活可防止软骨细胞去分化和纤维软骨形成。

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