Social stress induces neurovascular pathology promoting depression.
Caroline MénardMadeline L PfauGeorgia E HodesVeronika KanaVictoria X WangSylvain BouchardAki TakahashiMeghan E FlaniganHossein AleyasinKatherine B LeClairWilliam G JanssenBenoit LabontéEric M PariseZachary S LorschSam A GoldenMitra HeshmatiCarol TammingaGustavo TureckiMatthew CampbellZahi A FayadCheuk Ying TangMiriam MeradScott J RussoPublished in: Nature neuroscience (2017)
Studies suggest that heightened peripheral inflammation contributes to the pathogenesis of major depressive disorder. We investigated the effect of chronic social defeat stress, a mouse model of depression, on blood-brain barrier (BBB) permeability and infiltration of peripheral immune signals. We found reduced expression of the endothelial cell tight junction protein claudin-5 (Cldn5) and abnormal blood vessel morphology in nucleus accumbens (NAc) of stress-susceptible but not resilient mice. CLDN5 expression was also decreased in NAc of depressed patients. Cldn5 downregulation was sufficient to induce depression-like behaviors following subthreshold social stress whereas chronic antidepressant treatment rescued Cldn5 loss and promoted resilience. Reduced BBB integrity in NAc of stress-susceptible or mice injected with adeno-associated virus expressing shRNA against Cldn5 caused infiltration of the peripheral cytokine interleukin-6 (IL-6) into brain parenchyma and subsequent expression of depression-like behaviors. These findings suggest that chronic social stress alters BBB integrity through loss of tight junction protein Cldn5, promoting peripheral IL-6 passage across the BBB and depression.
Keyphrases
- blood brain barrier
- major depressive disorder
- depressive symptoms
- poor prognosis
- healthcare
- mental health
- cerebral ischemia
- sleep quality
- mouse model
- transcription factor
- stress induced
- endothelial cells
- binding protein
- type diabetes
- oxidative stress
- heat stress
- chemotherapy induced
- end stage renal disease
- signaling pathway
- prognostic factors
- metabolic syndrome
- mass spectrometry
- newly diagnosed
- long non coding rna
- social support
- brain injury
- peritoneal dialysis
- amino acid
- adipose tissue
- wild type