Singhal Gaurav, Morgan Julie, Jawahar Magdalene C, Corrigan Frances, Jaehne Emily J, Toben Catherine, Manavis Jim, Hannan Anthony J, Baune Bernhard T
Psychiatric Neuroscience Lab, Discipline of Psychiatry, The University of Adelaide, Adelaide, SA, Australia.
Division of Health Sciences, The University of South Australia, Adelaide, SA, Australia.
Front Cell Neurosci. 2020 Mar 18;14:57. doi: 10.3389/fncel.2020.00057. eCollection 2020.
Environmental enrichment (EE) has been shown to modulate behavior and immunity. We recently reported that both short and long-term EE enhance baseline locomotion and alleviate depressive-like behavior, but only long-term EE affects locomotion adversely in a threatening environment and enhances anxiety-like behavior in middle-age mice. We have now investigated whether the observed changes in behavior after short- and long-term EE were associated with underlying immune changes. Hence, at the end of behavioral testing, mice were sacrificed, and brains and cervical lymph nodes were collected to investigate the differential effects of the duration of EE (short- and long-term) on the number of immunopositive glial cells in the dentate gyrus, CA1, CA2, and CA3 regions of the hippocampus and proportions of T cell subsets in the cervical lymph nodes using immunohistochemistry and flow cytometry, respectively. EE, regardless of duration, caused an increase in microglia number within the dentate gyrus, CA1 and CA3 hippocampal regions, but only long-term EE increased astrocytes number within the dentate gyrus and CA3 hippocampal regions. A significantly higher proportion of CD8 naive T cells was observed after long-term EE vs. short-term EE. No significant differences were observed in the proportion of central memory and effector memory T cells or early activated CD25 cells between any of the test groups. Our results suggest that EE, irrespective of duration, enhances the numbers of microglia, but long-term EE is required to modify astrocyte number and peripheral T cell proportions in middle-aged mice. Our findings provide new insights into the therapeutic effects of EE on various brain disorders, which may be at least partly mediated by glial and neuroimmune modulation.
环境富集(EE)已被证明可调节行为和免疫。我们最近报告称,短期和长期的EE均可增强基线运动能力并减轻抑郁样行为,但只有长期EE会在威胁环境中对运动产生不利影响,并增强中年小鼠的焦虑样行为。我们现在研究了短期和长期EE后观察到的行为变化是否与潜在的免疫变化有关。因此,在行为测试结束时,处死小鼠并收集大脑和颈部淋巴结,分别使用免疫组织化学和流式细胞术研究EE持续时间(短期和长期)对海马齿状回、CA1、CA2和CA3区域免疫阳性神经胶质细胞数量以及颈部淋巴结中T细胞亚群比例的差异影响。无论持续时间如何,EE都会导致齿状回、海马CA1和CA3区域内的小胶质细胞数量增加,但只有长期EE会增加齿状回和海马CA3区域内的星形胶质细胞数量。与短期EE相比,长期EE后观察到CD8幼稚T细胞的比例显著更高。在任何测试组之间,中央记忆T细胞、效应记忆T细胞或早期活化的CD25细胞的比例均未观察到显著差异。我们的结果表明,无论持续时间如何,EE都会增加小胶质细胞的数量,但需要长期EE来改变中年小鼠的星形胶质细胞数量和外周T细胞比例。我们的研究结果为EE对各种脑部疾病的治疗作用提供了新的见解,这可能至少部分是由神经胶质和神经免疫调节介导的。