限制CD4+ T细胞受体库通过改变Th2细胞因子水平损害认知功能。

Neurogenesis (Austin, Tex.) Pub Date : 2017-01-05 eCollection Date: 2017-01-01 DOI:10.1080/23262133.2016.1256856
Eun Ji Song, Seong Gak Jeon, Kyoung Ah Kim, Jin-Il Kim, Minho Moon
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引用次数: 9

摘要

尽管CD4+ T细胞功能障碍对认知和行为障碍的影响已经确立,但在限制性CD4+ T细胞受体(TCR)库模型中,Th2细胞因子对成年海马神经发生和认知功能的影响尚未完全阐明。我们发现CD4+库TCR受限的小鼠使用OT-II小鼠后,海马神经发生减少。此外,我们证明OT-II小鼠外周器官中Th2细胞因子水平和大脑中IL-4水平升高。综上所述,Th2细胞因子水平的改变可能通过限制CD4+库TCR小鼠成年神经发生受损而影响学习和记忆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Restricted CD4+ T cell receptor repertoire impairs cognitive function via alteration of Th2 cytokine levels.

Despite the effects of CD4+ T cell dysfunction on cognitive and behavioral impairment are well established, the effects of Th2 cytokines on the adult hippocampal neurogenesis and cognitive function in restricted CD4+ T cell receptor (TCR) repertoire model have not been fully elucidate. We found that mice with restricted CD4+ repertoire TCR showed decreased adult hippocampal neurogenesis using OT-II mice. Moreover, we demonstrated that OT-II mice showed increased Th2 cytokine levels in peripheral organs and IL-4 levels in brain. Taken together, altered Th2 cytokine levels may impact learning and memory via impaired adult neurogenesis in restricted CD4+ repertoire TCR mice.

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