首页> 美国卫生研究院文献>Translational Psychiatry >CD4+ but not CD8+ T cells revert the impaired emotional behavior of immunocompromised RAG-1-deficient mice
【2h】

CD4+ but not CD8+ T cells revert the impaired emotional behavior of immunocompromised RAG-1-deficient mice

机译:CD4 +而非CD8 + T细胞可逆转免疫受损的RAG-1缺陷小鼠的受损情绪行为

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

An imbalanced immune system has long been known to influence a variety of mood disorders including anxiety, obsessive-compulsive disorders and depression. In this study, we sought to model the impact of an immunocompromised state on these emotional behaviors using RAG-1−/− mice, which lack T and B cells. We also investigated the relative contribution of CD4+ or CD8+ T cells to these manifestations using RAG-1−/−/OT-II and RAG-1−/−/OT-I transgenic mice, respectively. Our results show that RAG-1−/− mice present a significant increase in digging and marble-burying activities compared with wild-type mice. Surprisingly, these anxiety-like behaviors were significantly reverted in RAG-1−/−/OT-II but not RAG-1−/−/OT-I transgenic mice. Immunodepletion experiments with anti-CD4 or anti-CD8 in C57/BL6 mice or repopulation studies in RAG-1−/− mice did not reproduce these findings. Microarray analysis of the brain of RAG-1−/− and RAG-1−/−/OT-II mice revealed a significantly different gene fingerprint, with the latter being more similar to wild-type mice than the former. Further analysis revealed nine main signaling pathways as being significantly modulated in RAG-1−/− compared with wild-type mice. Taken together, these results suggest that life-long rather than transient immunodeficient conditions influence the emotional behaviors in mice. Most interestingly, these effects seem to correlate with a specific absence of CD4+ rather than CD8+ T cells. Validation of these findings in man might provide new clues on the mechanism by which early life immune modulation might impact mood response in adults and provide a further link between immune and emotional well-being.
机译:长期以来已知免疫系统失衡会影响多种情绪障碍,包括焦虑症,强迫症和抑郁症。在这项研究中,我们试图使用缺乏T细胞和B细胞的RAG-1 -/-小鼠来模拟免疫受损状态对这些情绪行为的影响。我们还使用RAG-1 -/- / OT-II和CD-MS研究了CD4 + 或CD8 + T细胞对这些表现的相对贡献。 RAG-1 -/- / OT-1转基因小鼠。我们的结果表明,与野生型小鼠相比,RAG-1 -/-小鼠的挖掘和大理石掩埋活动显着增加。令人惊讶的是,这些焦虑样行为在RAG-1 -/- / OT-II中得到了显着恢复,而RAG-1 -/- / OT-I转基因小鼠却没有得到恢复。在C57 / BL6小鼠中使用抗CD4或抗CD8进行的免疫减少实验或在RAG-1 -/-小鼠中进行的种群研究并未重现这些发现。对RAG-1 -/-和RAG-1 -/- / OT-II小鼠的大脑进行的微阵列分析显示,基因指纹显着不同,后者更为明显野生型小鼠比前者相似。进一步的分析表明,与野生型小鼠相比,RAG-1 -/-中有9条主要信号通路被显着调节。综上所述,这些结果表明,终生而非短暂的免疫缺陷病会影响小鼠的情绪行为。最有趣的是,这些效应似乎与CD4 + 而不是CD8 + T细胞的特定缺失有关。这些发现在人类中的验证可能提供有关生命早期免疫调节可能影响成年人情绪反应的机制的新线索,并提供免疫与情绪健康之间的进一步联系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号