Neuroimmune Contributions to TlymphocyteDriven Inflammation in a Preclinical Model of Posttraumatic Stress Disorder (PTSD)
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Posttraumatic stress disorder (PTSD) is a devastating psychological disorder with an idiopathic etiology. Interestingly, patients with PTSD have a >3 fold risk of developing comorbid autoimmune diseases compared to matched controls, yet, the exact mechanisms underlying this risk remain unclear. A hallmark of PTSD is increased sympathetic tone, and previous work from our lab has shown that immune cells, primarily Tlymphocytes, display an autoreactive phenotype when exposed to elevated levels of norepinephrine (NE). Therefore, we hypothesized that the sympathoexcitation observed in PTSD may be causally linked to Tlymphocytedriven inflammation and the predisposition to autoimmune diseases. To test this hypothesis, we adapted a preclinical mouse model of PTSD known as social defeat stress. After validating the PTSDlike behavioral phenotype of our traumaexposed mice, we investigated the neuroimmune interactions of Tlymphocytes in the spleen that may govern the increased predilection for inflammatory diseases in PTSD patients. The spleen is a primary site of adaptive immune system activation, and is innervated exclusively by the sympathetic efferent splenic nerve. Traumaexposed animals exhibited a 2.5 fold increase in splenic catecholamines and 4.1 fold increase in splenic tyrosine hydroxylase (TH) content (p<0.05) compared to controls. Additionally, purified splenic Tlymphocytes from sociallydefeated mice showed elevations in the proinflammatory cytokines interleukin 6 (IL6, 1.84 fold increase, p<0.0001) and interleukin 17A (IL17A, 5.5 fold increase, p=0.0032). Importantly, TH content was tightly correlated with Tlymphocyte IL6 and IL17A expression (R=0.43, p=0.0001 and R=0.87, p<0.0001, respectively), suggesting a neuroimmune mechanism of proinflammation. To test this, we performed targeted splenic denervation to deduce the contribution of the splenic nerve to Tlymphocytedriven inflammation after psychological trauma. Denervation reduced splenic NE content by 80% (p<0.0001), and persisted to at least 30 days after denervation. While splenic denervation did not alter the PTSDlike behavioral changes after social defeat, denervation ameliorated the characteristic increase in gene expression of splenic Tlymphocyte IL6 and IL17A after social defeat stress. Overall, our data suggest that psychological trauma results in altered inflammation through sympathetic modulation of splenic Tlymphocytes. Further elucidation of this neuroimmune interaction will provide possible new biomarkers or therapeutic strategies to reduce the inflammatorydriven morbidity and mortality of PTSD patients.Support or Funding InformationNIH R00HL123471, T32NS105594
