首页> 外文会议>European Symposium on Life Sciences in Space >MICROGRAVITY AND SIGNALING MOLECULES IN RAT OSTEOBLASTS: DOWNSTREAM OF RECEPTOR TYROSINE KINASE, G-PROTEIN-COUPLED RECEPTOR, AND SMALL GTP-BINDING PROTEINS
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MICROGRAVITY AND SIGNALING MOLECULES IN RAT OSTEOBLASTS: DOWNSTREAM OF RECEPTOR TYROSINE KINASE, G-PROTEIN-COUPLED RECEPTOR, AND SMALL GTP-BINDING PROTEINS

机译:大鼠成骨细胞中的微匍匐和信号分子:受体酪氨酸激酶,G蛋白偶联受体和小GTP结合蛋白的下游

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Rat osteoblasts were cultured for 4 and 5 days aboard Space Shuttle and solubilized on board. The mRNA levels of the post-receptor signaling molecules were analyzed by quantitative RT-PCR. The G-protein α subunit Gαq mRNA levels were elevated 3-fold by microgravity. Gαq stimulates PLCβ, and then PKC. PKCδ and PKCv mRNA levels were increased 2- to 5-fold by microgravity. The mRNA levels of SOS and Ras GRF were increased 4 to 5-fold by microgravity, while Ras GAP was not altered. Spaceflight-induced bone loss might be attributed to microgravity modulation of the signaling pathway in osteoblasts.
机译:将大鼠成骨细胞培养4至5天,在航天飞机和溶解的船上溶解。通过定量RT-PCR分析受体后信号传导分子的mRNA水平。 G蛋白α亚基GαQmRNA水平通过微匍匐升高3倍。 GαQ刺激PLCβ,然后是PKC。 PKCδ和PKCV mRNA水平通过微匍匐增加2-5倍。通过微匍匐,SOS和RAS GR的mRNA水平增加4至5倍,而RAS间隙未被改变。诱导的骨质损失可能归因于成骨细胞中信号通路的微匍匐调制。

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