Composition and Organization of Acute Ischemic Stroke Thrombus: A Wealth of Information for Future Thrombolytic Strategies.

fibrin ischemic stroke neutrophil extracellular traps (NETs) platelet aggregates thrombus composition von Willebrand factor (vWF)

Journal

Frontiers in neurology
ISSN: 1664-2295
Titre abrégé: Front Neurol
Pays: Switzerland
ID NLM: 101546899

Informations de publication

Date de publication:
2022
Historique:
received: 06 02 2022
accepted: 18 05 2022
entrez: 25 7 2022
pubmed: 26 7 2022
medline: 26 7 2022
Statut: epublish

Résumé

During the last decade, significant progress has been made in understanding thrombus composition and organization in the setting of acute ischemic stroke (AIS). In particular, thrombus organization is now described as highly heterogeneous but with 2 preserved characteristics: the presence of (1) two distinct main types of areas in the core-red blood cell (RBC)-rich and platelet-rich areas in variable proportions in each thrombus-and (2) an external shell surrounding the core composed exclusively of platelet-rich areas. In contrast to RBC-rich areas, platelet-rich areas are highly complex and are mainly responsible for the thrombolysis resistance of these thrombi for the following reasons: the presence of platelet-derived fibrinolysis inhibitors in large amounts, modifications of the fibrin network structure resistant to the tissue plasminogen activator (tPA)-induced fibrinolysis, and the presence of non-fibrin extracellular components, such as von Willebrand factor (vWF) multimers and neutrophil extracellular traps. From these studies, new therapeutic avenues are in development to increase the fibrinolytic efficacy of intravenous (IV) tPA-based therapy or to target non-fibrin thrombus components, such as platelet aggregates, vWF multimers, or the extracellular DNA network.

Identifiants

pubmed: 35873787
doi: 10.3389/fneur.2022.870331
pmc: PMC9298929
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

870331

Informations de copyright

Copyright © 2022 Desilles, Di Meglio, Delvoye, Maïer, Piotin, Ho-Tin-Noé and Mazighi.

Déclaration de conflit d'intérêts

J-PD, MM, BH-T-N, MP, and LD are co-inventors of the following patent: Methods and pharmaceutical compositions for the treatment of acute ischemic stroke (PCT/EP2018/062588). The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Jean-Philippe Desilles (JP)

Interventional Neuroradiology Department and Biological Resources Center, Rothschild Foundation Hospital, Paris, France.
Laboratory of Vascular Translational Science, U1148 INSERM, Paris, France.
Université Paris Cité, Paris, France.
FHU Neurovasc, Paris, France.

Lucas Di Meglio (L)

Laboratory of Vascular Translational Science, U1148 INSERM, Paris, France.

Francois Delvoye (F)

Interventional Neuroradiology Department and Biological Resources Center, Rothschild Foundation Hospital, Paris, France.
University of Liège, Liege, Belgium.

Benjamin Maïer (B)

Interventional Neuroradiology Department and Biological Resources Center, Rothschild Foundation Hospital, Paris, France.
Université Paris Cité, Paris, France.
FHU Neurovasc, Paris, France.

Michel Piotin (M)

Interventional Neuroradiology Department and Biological Resources Center, Rothschild Foundation Hospital, Paris, France.
Laboratory of Vascular Translational Science, U1148 INSERM, Paris, France.

Benoît Ho-Tin-Noé (B)

Laboratory of Vascular Translational Science, U1148 INSERM, Paris, France.
Université Paris Cité, Paris, France.

Mikael Mazighi (M)

Interventional Neuroradiology Department and Biological Resources Center, Rothschild Foundation Hospital, Paris, France.
Laboratory of Vascular Translational Science, U1148 INSERM, Paris, France.
Université Paris Cité, Paris, France.
FHU Neurovasc, Paris, France.
Department of Neurology, Hopital Lariboisère, APHP Nord, Paris, France.

Classifications MeSH