Platelets and Immune Responses During Thromboinflammation.
Animals
Blood Platelets
/ immunology
Bone Marrow
Complement System Proteins
/ immunology
Disease Susceptibility
Humans
Immunity
Immunity, Innate
Inflammation
/ etiology
Platelet Activation
Platelet Membrane Glycoproteins
/ metabolism
Protein Binding
Signal Transduction
Thrombopoiesis
Thrombosis
/ etiology
EAE
complement
infection
inflammation
innate immunity
platelets
stroke
tissue remodeling
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2019
2019
Historique:
received:
15
03
2019
accepted:
09
07
2019
entrez:
13
8
2019
pubmed:
14
8
2019
medline:
21
10
2020
Statut:
epublish
Résumé
Besides mediating hemostatic functions, platelets are increasingly recognized as important players of inflammation. Data from experiments in mice and men revealed various intersection points between thrombosis, hemostasis, and inflammation, which are addressed and discussed in this review in detail. One such example is the intrinsic coagulation cascade that is initiated after platelet activation thereby further propagating and re-enforcing wound healing or thrombus formation but also contributing to the pathophysiology of severe diseases. FXII of the intrinsic pathway connects platelet activation with the coagulation cascade during immune reactions. It can activate the contact system thereby either creating an inflammatory state or accelerating inflammation. Recent insights into platelet biology could show that platelets are equipped with complement receptors. Platelets are important for tissue remodeling after injury has been inflicted to the endothelial barrier and to the subendothelial tissue. Thus, platelets are increasingly recognized as more than just cells relevant for bleeding arrest. Future insights into platelet biology are to be expected. This research will potentially offer novel opportunities for therapeutic intervention in diseases featuring platelet abundance.
Identifiants
pubmed: 31402914
doi: 10.3389/fimmu.2019.01731
pmc: PMC6676797
doi:
Substances chimiques
Platelet Membrane Glycoproteins
0
Complement System Proteins
9007-36-7
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
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