首页> 外文期刊>Biotechnology and Applied Biochemistry >Comparison of JNK (c-Jun N-terminal kinase)-like MAPK (mitogen-activated protein kinase) phosphorylation between immobilized cultures and Couette-type shear reactor cultures of Taxus cuspidata (Japanese yew) cells
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Comparison of JNK (c-Jun N-terminal kinase)-like MAPK (mitogen-activated protein kinase) phosphorylation between immobilized cultures and Couette-type shear reactor cultures of Taxus cuspidata (Japanese yew) cells

机译:东北红豆杉固定化培养物与库埃特型剪切反应器培养物之间JNK(c-Jun N-末端激酶)样MAPK(丝裂原活化蛋白激酶)磷酸化的比较

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摘要

The signal mechanism of Taxus cuspidata (Japanese yew) cells involved in response to shear stress and immobilized matrices was investigated. Western-blot analysis showed that the immobilized cultures altered the degree of phosphorylation of the JNK (c-Jun N-terminal kinase)-like and a 41 kDa p38-like MAPKs (mitogen-activated protein kinases), particularly the 52 and 45 kDa JNK-like MAPKs. The increased rotation speeds up-regulated the degree of phosphorylation of 45 and 47 kDa JNK-like MAPKs, whereas the 41 kDa p38-like MAPK was not significantly changed. The level of phosphorylation of JNK-like MAPKs in the outer zone cells of immobilized matrices was the highest among the different zone cells, which was identical with that of T. cuspidata cells exposed to hydrodynamic shear stresses. The highly specific p38- or JNK-MAPK inhibitors strongly reduced respectively the p38- or JNK-like MAPK phosphorylation, which also demonstrated that there were no cross-reactions between the p38-like MAPK and JNK-like MAPK in T cuspidata cells. By a comparison of the effects of the immobilization and laminar shear stress on the phosphorylation of p38-and JNK-like MAPKs in T cuspidata cells, these findings suggested that the JNK-like MAPK signal pathways may be involved in I cuspidata cell response to the hydrodynamic shear stress, rather than to the p38-like MARK.
机译:研究了红豆杉细胞对剪应力和固定化基质的响应所涉及的信号机制。 Western印迹分析表明,固定的培养物改变了JNK(c-Jun N端激酶)样和41 kDa p38样MAPK(促分裂原激活的蛋白激酶)的磷酸化程度,尤其是52 kDa和45 kDa类似于JNK的MAPK。增加的旋转速度上调了45和47 kDa的JNK样MAPK的磷酸化程度,而41 kDa的p38样MAPK没有明显改变。在不同区域的细胞中,固定化基质的外部区域细胞中JNK样MAPKs的磷酸化水平最高,与暴露于水动力剪切应力下的虎杖细胞相同。高度特异性的p38-或JNK-MAPK抑制剂分别强烈降低了p38-或JNK-样MAPK的磷酸化,这也表明T cuspidata细胞中p38-样MAPK和JNK-样MAPK之间没有交叉反应。通过比较固定化和层流切应力对T cuspidata细胞中p38和JNK样MAPK磷酸化的影响,这些发现表明JNK like MAPK信号通路可能参与了I cuspidata细胞对T的反应。流体动力剪切应力,而不是p38样的MARK。

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