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Pivotal Advance: Nonfunctional lung effectors exhibit decreased calcium mobilization associated with reduced expression of ORAI1

机译:关键进展:非功能性肺效应子的钙动员减少与ORAI1表达降低相关

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摘要

CD8+ T cells play a critical role in the clearance of respiratory pathogens. Thus, it is surprising that functional inactivation of lung effectors has been observed in many models of viral infection. Currently, the molecular defect responsible for the shut-off of function in these cells is unknown. In the present study, we addressed this question using a model of respiratory infection with the paramyxovirus SV5. Nonfunctional cells were found to exhibit decreases in SOCE, resulting in reduced NFAT1 activation. Notably, function could be restored by the provision of increased levels of extracellular calcium. The reduced ability to mobilize calcium was associated with reduced expression of ORAI1, the CRAC channel subunit. These findings reveal a previously unknown mechanism for the negative regulation of function in effector T cells.
机译:CD8 + T细胞在清除呼吸道病原体中起关键作用。因此,令人惊讶的是,在许多病毒感染模型中已经观察到肺效应子的功能失活。目前,尚不清楚负责关闭这些细胞功能的分子缺陷。在本研究中,我们使用副粘病毒SV5的呼吸道感染模型解决了这个问题。发现非功能性细胞的SOCE降低,导致NFAT1激活降低。值得注意的是,可以通过提供增加水平的细胞外钙来恢复功能。动员钙的能力降低与CRAC通道亚基ORAI1的表达降低有关。这些发现揭示了在效应T细胞中负调节功能的先前未知的机制。

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