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JNK1 controls adult hippocampal neurogenesis and imposes cell-autonomous control of anxiety behaviour from the neurogenic niche

机译:JNK1控制成人海马神经发生,并从神经源性利基处施加对焦虑行为的细胞自主控制

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Promoting adult hippocampal neurogenesis is expected to induce neuroplastic changes that improve mood and alleviate anxiety. However, the underlying mechanisms remain largely unknown and the hypothesis itself is controversial. Here we show that mice lacking Jnk1 , or c-Jun N-terminal kinase (JNK) inhibitor-treated mice, display increased neurogenesis in adult hippocampus characterized by enhanced cell proliferation and survival, and increased maturation in the ventral region. Correspondingly, anxiety behaviour is reduced in a battery of tests, except when neurogenesis is prevented by AraC treatment. Using engineered retroviruses, we show that exclusive inhibition of JNK in adult-born granule cells alleviates anxiety and reduces depressive-like behaviour. These data validate the neurogenesis hypothesis of anxiety. Moreover, they establish a causal role for JNK in the hippocampal neurogenic niche and anxiety behaviour, and advocate targeting of JNK as an avenue for novel therapies against affective disorders.
机译:预期促进成年海马神经发生可诱导神经塑性改变,从而改善情绪并减轻焦虑。但是,基本的机制仍然是未知的,并且该假设本身是有争议的。在这里,我们显示缺少iNK1或c-Jun N末端激酶(JNK)抑制剂治疗的小鼠的小鼠在成年海马中表现出增加的神经发生,其特征是细胞增殖和存活增强,在腹侧区域成熟。相应地,一系列测试减少了焦虑行为,除非通过AraC治疗可防止神经发生。使用工程改造的逆转录病毒,我们表明,JNK在成年出生的颗粒细胞中的排他性抑制可缓解焦虑症,并降低抑郁样行为。这些数据证实了焦虑的神经发生假说。此外,他们在海马神经源性利基和焦虑行为中建立了JNK的因果作用,并提倡针对JNK作为针对情感障碍的新疗法的途径。

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