首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >CLINOROTATION DIFFERENTIALLY INHIBITS T-LYMPHOCYTE TRANSCRIPTION FACTOR ACTIVATION
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CLINOROTATION DIFFERENTIALLY INHIBITS T-LYMPHOCYTE TRANSCRIPTION FACTOR ACTIVATION

机译:气候分异不同地抑制了T淋巴细胞转录因子的激活

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摘要

T lymphocytes cultured under the low-shear stress environment of modeled microgravity demonstrate an inhibition of activation in response to T-cell receptor (TCR)-mediated signaling. Modeled microgravity culture-induced inhibition mimics the inhibition observed during spaceflight. This work investigates the molecular signaling events of interleukin 2 transcription activation in modeled microgravity as generated with clinorotation. Under normal conditions, NFAT (nuclear factor of activated T cells) isdephosphorylated and activated with sustained calcium (Ca~+) influx and calcineurin activity, whereas AP-1 is activated by protein kinase C (PKC) and Ras-mediated pathways. Purified human T lymphocytes are shown to exhibit differential inhibition of transcription factor activation in modeled microgravity. Activation of AP-1 is blocked with clinorotation, whereas NFAT dephosphorylation occurs. This work supports the theory that modeled microgravity differentially blocks the activation of distinct signaling mechanism.
机译:在模拟微重力的低剪切应力环境下​​培养的T淋巴细胞表现出对T细胞受体(TCR)介导的信号传导的抑制作用。建模的微重力培养物诱导的抑制模仿了太空飞行中观察到的抑制。这项工作调查白细胞介素2转录激活的模拟微重力中由clinorotation生成的分子信号事件。在正常情况下,NFAT(活化的T细胞的核因子)被去磷酸化并被持续的钙(Ca〜+)流入和钙调神经磷酸酶活性所激活,而AP-1被蛋白激酶C(PKC)和Ras介导的途径激活。纯化的人T淋巴细胞在模拟微重力下显示出对转录因子激活的不同抑制作用。 AP-1的激活被倾斜旋转阻止,而NFAT发生脱磷酸作用。这项工作支持微重力建模差异地阻止独特信号机制激活的理论。

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