TY - JOUR
T1 - Blood–brain crosstalk
T2 - the roles of neutrophils, platelets, and neutrophil extracellular traps in neuropathologies
AU - Chou, Ming Li
AU - Babamale, Abdulkareem Olarewaju
AU - Walker, Tara L.
AU - Cognasse, Fabrice
AU - Blum, David
AU - Burnouf, Thierry
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/9
Y1 - 2023/9
N2 - Systemic inflammation, neurovascular dysfunction, and coagulopathy often occur concurrently in neuropathologies. Neutrophils and platelets have crucial synergistic roles in thromboinflammation and are increasingly suspected as effector cells contributing to the pathogenesis of neuroinflammatory diseases. In this review, we summarize the roles of platelet–neutrophil interactions in triggering complex pathophysiological events affecting the brain that may lead to the disruption of brain barriers, infiltration of toxic factors into the parenchyma, and amplification of neuroinflammation through the formation of neutrophil extracellular traps (NETs). We highlight the clinical significance of thromboinflammation in neurological disorders and examine the contributions of damage-associated molecular patterns (DAMPs) derived from platelets and neutrophils. These DAMPs originate from both infectious and non-infectious risk factors and contribute to the activation of inflammasomes during brain disorders. Finally, we identify knowledge gaps in the molecular mechanisms underlying neurodegenerative disease pathogenesis and emphasize the potential of interventions targeting platelets and neutrophils to treat neuroinflammatory diseases.
AB - Systemic inflammation, neurovascular dysfunction, and coagulopathy often occur concurrently in neuropathologies. Neutrophils and platelets have crucial synergistic roles in thromboinflammation and are increasingly suspected as effector cells contributing to the pathogenesis of neuroinflammatory diseases. In this review, we summarize the roles of platelet–neutrophil interactions in triggering complex pathophysiological events affecting the brain that may lead to the disruption of brain barriers, infiltration of toxic factors into the parenchyma, and amplification of neuroinflammation through the formation of neutrophil extracellular traps (NETs). We highlight the clinical significance of thromboinflammation in neurological disorders and examine the contributions of damage-associated molecular patterns (DAMPs) derived from platelets and neutrophils. These DAMPs originate from both infectious and non-infectious risk factors and contribute to the activation of inflammasomes during brain disorders. Finally, we identify knowledge gaps in the molecular mechanisms underlying neurodegenerative disease pathogenesis and emphasize the potential of interventions targeting platelets and neutrophils to treat neuroinflammatory diseases.
KW - extracellular vesicles
KW - neurodegeneration
KW - neuroimmune
KW - neuroinflammation
KW - Thromboinflammation
KW - viral infection
UR - http://www.scopus.com/inward/record.url?scp=85165633722&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85165633722&partnerID=8YFLogxK
U2 - 10.1016/j.tins.2023.06.005
DO - 10.1016/j.tins.2023.06.005
M3 - Review article
C2 - 37500363
AN - SCOPUS:85165633722
SN - 0166-2236
VL - 46
SP - 764
EP - 779
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - 9
ER -