FKBP5 and early life stress affect the hippocampus by an age-dependent mechanism

• Main Authors: Marangelie Criado-Marrero, Taylor M. Smith, Lauren A. Gould, Sojeong Kim, Hannah J. Penny, Zheying Sun, Danielle Gulick, Chad A. Dickey, Laura J. Blair
• Format: Article
• Language: English
• Published: Elsevier 2020-12-01
• Series: Brain, Behavior, & Immunity - Health
• Subjects: Hippocampus; FKBP5; Early life stress; Maternal separation; Glucocorticoids; Stress
• Online Access: http://www.sciencedirect.com/science/article/pii/S2666354620301083

Early life stress (ELS) adversely affects the brain and is commonly associated with the etiology of mental health disorders, like depression. In addition to the mood-related symptoms, patients with depression show dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis, increased peripheral inflammation, and structural brain alterations. Although the underlying causes are unknown, polymorphisms in the FK506-binding protein 5 (FKBP5) gene, a regulator of glucocorticoid receptor (GR) activity, interact with childhood adversities to increase vulnerability to depressive disorders. We hypothesized that high FKBP5 protein levels combined with early life stress (ELS) would alter the HPA axis and brain, promoting depressive-like behaviors. To test this, we exposed males and females of a mouse model overexpressing FKBP5 in the brain (rTgFKBP5 mice), or littermate controls, to maternal separation for 14 days after birth. Then, we evaluated neuroendocrine, behavioral, and brain changes in young adult and aged mice. We observed lower basal corticosterone (CORT) levels in rTgFKBP5 mice, which was exacerbated in females. Aged, but not young, rTgFKBP5 mice showed increased depressive-like behaviors. Moreover, FKBP5 overexpression reduced hippocampal neuron density in aged mice, while promoting markers of microglia expression, but these effects were reversed by ELS. Together, these results demonstrate that high FKBP5 affects basal CORT levels, depressive-like symptoms, and numbers of neurons and microglia in the hippocampus in an age-dependent manner.