Abstract
The role of platelets in hemostasis and thrombosis has long been recognized, recently their contribution to immunological and inflammatory processes is emerging. Platelets could be the missing link between cardiovascular disease, chronic stress and depressive symptoms. Both physical and mental stressors cause platelet activation reflected by changes in platelet bioactivity and aggregation. Here we evaluate the proinflammatory platelet response to acute and chronic mental stress. In a prospective study design an acute mental stress test was administered to 55 healthy male participants once without and once in the presence of chronic mental stress. Blood was collected prior to and at three time points following an acute mental stress test (0, 30, 60 min). Platelet proinflammatory activation markers, were assessed using FACS analysis and aggregability was measured in response to ADP or epinephrine using PFA-100. A linear mixed model was used for analysis. Chronic mental stress lead to a significant increase in state anxiety (p < 0.001), depressive symptoms (p = 0.045) and perceived stress (p = 0.001). The factor “chronic mental stress” was significantly associated with increased numbers of CD63+ platelets (p = 0.009). The factor “acute mental stress” was associated with alterations in CD62P+ platelets (p < 0.001), CD63+ platelets (p = 0.011), PAC-1+ platelets (p < 0.001) as well as platelet leucocyte aggregates (p = 0.019). The recovery of CD62P function following the acute mental stress exposure was significantly impaired by chronic stress (p = 0.023). Aggregation was affected by chronic and acute mental stress. In conclusion, mental stress is linked to an increased and prolonged proinflammatory platelet bioactivity. This proinflammatory and immunomodulatory stimuli could help to explain the link between mental and somatic disorders.Graphical
Highlights
Pia Koudouovoh-Tripp and Katharina Hüfner contributed to this work.Platelets are the smallest cell fragments in the human body, (Jurk and Kehrel 2005)
In order to determine the expression of activation markers on platelets, a mix of the following antibodies, PAC-1 FITC, CD63-PE (HSC6), CD62P-APC (AK-4), and CD42b-PerCP (HIP1, Biolegend), was
In the present study we found a prolonged proinflammatory platelet response for CD62P in the chronic mental stress condition
Summary
Platelets are the smallest cell fragments in the human body, (Jurk and Kehrel 2005). Known for their effector role in hemostasis, thrombosis and wound healing, recent investigations have highlighted their engagement in the immune system. Platelets can be regarded as effector cells in the innate immune system They are able to cross talk with the adaptive immune system by secreting pro-inflammatory and immunomodulatory proteins (Semple et al 2011). These molecules are stored in three types of storage granules: dense granules, alpha granules, and lysosomes. The dense granules mainly store serotonin, adenosine diphosphate (ADP) and CD63 (Jurk and Kehrel 2005) while the alpha granules store
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