Department of Psychology, University of Maryland, College Park, MD 20742, USA; Program in Neuroscience and Cognitive Sciences, University of Maryland, College Park, MD 20742, USA; Department of Biology, Hope College, Holland, MI 49423, USA.
Department of Psychology, University of Maryland, College Park, MD 20742, USA.
Brain Behav Immun. 2022 Nov;106:1-10. doi: 10.1016/j.bbi.2022.07.161. Epub 2022 Jul 28.
Adverse early-life experiences are risk factors for psychiatric disease development, resulting in stress-related neuronal modeling and neurobehavioral changes. Stressful experiences modulate the immune system, contributing to neuronal damage in higher cortical regions, like the hippocampus. Moreover, early-life stressors dysregulate the function of microglia, the resident immune cells of the brain, in the developing hippocampus. Paternal deprivation, an early-life stressor in many biparental species, facilitates sex-dependent inhibitions in hippocampal plasticity, but parental contributors to these sex-specific outcomes are unknown. Also, neurobiological mechanisms contributing to impairments in hippocampal neuroplasticity are less known. Thus, our goals were to 1) determine whether parental behavior is altered in maternal females following removal of the paternal male, 2) assess the effects of paternal deprivation on dentate gyrus (DG) volume and microglia proliferation, and 3) determine if early-life experimental handling mitigates sex-specific reductions in DG cell survival. California mice were born to multiparous breeders and reared by both parents (biparental care) or by their mother alone (i.e., father removed on postnatal day 1; paternal deprivation). One cohort of offspring underwent offspring retrieval tests for eight days beginning on postnatal day 2. On PND 68, these offspring (and a second cohort of mice without behavioral testing) were euthanized and brains visualized for bromodeoxyuridine (BrdU) and neuron-specific class III beta-tubulin (TuJ-1) or ionized calcium binding adaptor molecule 1 (Iba1). While mate absence did not impair maternal retrieval, paternal deprivation reduced DG volume, but Iba1+ cell density was only higher in paternally-deprived females. Neither sex or paternal deprivation significantly altered the number of BrdU+ or Tuj1+ cells in the DG - an absence of a reduction in cell survival may be related to daily handing during early offspring retrieval tests. Together, these data suggest that paternal deprivation impairs hippocampal plasticity; however, sex and early environment may influence the magnitude of these outcomes.
不良的早期生活经历是精神疾病发展的风险因素,导致与应激相关的神经元建模和神经行为改变。应激体验调节免疫系统,导致海马等高级皮质区域的神经元损伤。此外,早期生活应激源会使发育中的海马中海马体中的小胶质细胞(大脑的常驻免疫细胞)功能失调。在许多双亲种中,父爱剥夺是一种早期生活应激源,促进了海马体可塑性的性别依赖性抑制,但导致这些性别特异性结果的父母因素尚不清楚。此外,导致海马体神经可塑性受损的神经生物学机制知之甚少。因此,我们的目标是:1)确定在雄性父本被移除后,母本雌性的亲代行为是否发生改变;2)评估父爱剥夺对齿状回(DG)体积和小胶质细胞增殖的影响;3)确定早期生活实验性处理是否减轻了 DG 细胞存活的性别特异性减少。加利福尼亚鼠由多胎繁殖者所生,并由父母双方(双亲照料)或仅由其母亲(即,雄性父本在产后第 1 天被移除;父爱剥夺)共同抚养。一批后代从产后第 2 天开始进行为期 8 天的后代检索测试。在 PND68 时,这些后代(和另一批未进行行为测试的小鼠)被安乐死,并用溴脱氧尿苷(BrdU)和神经元特异性 III 类β-微管蛋白(TuJ-1)或离子钙结合衔接分子 1(Iba1)对大脑进行可视化处理。虽然伴侣缺失不会损害母本的检索,但父爱剥夺会减少 DG 体积,但只有父本剥夺的雌性小胶质细胞密度更高。无论是性别还是父爱剥夺都没有显著改变 DG 中的 BrdU+或 Tuj1+细胞数量-细胞存活没有减少可能与早期幼鼠检索测试期间的日常处理有关。综上所述,这些数据表明父爱剥夺会损害海马体的可塑性;然而,性别和早期环境可能会影响这些结果的程度。