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Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective

We have established considerable expertise in studying the role of platelets in cancer biology. From this expertise, we were keen to recognize the numerous venous-, arterial-, microvascular-, and macrovascular thrombotic events and immunologic disorders are caused by severe, acute-respiratory-syndro...

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Autores principales: Menter, David G., Afshar-Kharghan, Vahid, Shen, John Paul, Martch, Stephanie L., Maitra, Anirban, Kopetz, Scott, Honn, Kenneth V., Sood, Anil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754476/
https://www.ncbi.nlm.nih.gov/pubmed/35022962
http://dx.doi.org/10.1007/s10555-022-10019-5
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author Menter, David G.
Afshar-Kharghan, Vahid
Shen, John Paul
Martch, Stephanie L.
Maitra, Anirban
Kopetz, Scott
Honn, Kenneth V.
Sood, Anil K.
author_facet Menter, David G.
Afshar-Kharghan, Vahid
Shen, John Paul
Martch, Stephanie L.
Maitra, Anirban
Kopetz, Scott
Honn, Kenneth V.
Sood, Anil K.
author_sort Menter, David G.
collection PubMed
description We have established considerable expertise in studying the role of platelets in cancer biology. From this expertise, we were keen to recognize the numerous venous-, arterial-, microvascular-, and macrovascular thrombotic events and immunologic disorders are caused by severe, acute-respiratory-syndrome coronavirus 2 (SARS-CoV-2) infections. With this offering, we explore the evolutionary connections that place platelets at the center of hemostasis, immunity, and adaptive phylogeny. Coevolutionary changes have also occurred in vertebrate viruses and their vertebrate hosts that reflect their respective evolutionary interactions. As mammals adapted from aquatic to terrestrial life and the heavy blood loss associated with placentalization-based live birth, platelets evolved phylogenetically from thrombocytes toward higher megakaryocyte-blebbing-based production rates and the lack of nuclei. With no nuclei and robust RNA synthesis, this adaptation may have influenced viral replication to become less efficient after virus particles are engulfed. Human platelets express numerous receptors that bind viral particles, which developed from archetypal origins to initiate aggregation and exocytic-release of thrombo-, immuno-, angiogenic-, growth-, and repair-stimulatory granule contents. Whether by direct, evolutionary, selective pressure, or not, these responses may help to contain virus spread, attract immune cells for eradication, and stimulate angiogenesis, growth, and wound repair after viral damage. Because mammalian and marsupial platelets became smaller and more plate-like their biophysical properties improved in function, which facilitated distribution near vessel walls in fluid-shear fields. This adaptation increased the probability that platelets could then interact with and engulf shedding virus particles. Platelets also generate circulating microvesicles that increase membrane surface-area encounters and mark viral targets. In order to match virus-production rates, billions of platelets are generated and turned over per day to continually provide active defenses and adaptation to suppress the spectrum of evolving threats like SARS-CoV-2.
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spelling pubmed-87544762022-01-13 Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective Menter, David G. Afshar-Kharghan, Vahid Shen, John Paul Martch, Stephanie L. Maitra, Anirban Kopetz, Scott Honn, Kenneth V. Sood, Anil K. Cancer Metastasis Rev Non-Thematic Review We have established considerable expertise in studying the role of platelets in cancer biology. From this expertise, we were keen to recognize the numerous venous-, arterial-, microvascular-, and macrovascular thrombotic events and immunologic disorders are caused by severe, acute-respiratory-syndrome coronavirus 2 (SARS-CoV-2) infections. With this offering, we explore the evolutionary connections that place platelets at the center of hemostasis, immunity, and adaptive phylogeny. Coevolutionary changes have also occurred in vertebrate viruses and their vertebrate hosts that reflect their respective evolutionary interactions. As mammals adapted from aquatic to terrestrial life and the heavy blood loss associated with placentalization-based live birth, platelets evolved phylogenetically from thrombocytes toward higher megakaryocyte-blebbing-based production rates and the lack of nuclei. With no nuclei and robust RNA synthesis, this adaptation may have influenced viral replication to become less efficient after virus particles are engulfed. Human platelets express numerous receptors that bind viral particles, which developed from archetypal origins to initiate aggregation and exocytic-release of thrombo-, immuno-, angiogenic-, growth-, and repair-stimulatory granule contents. Whether by direct, evolutionary, selective pressure, or not, these responses may help to contain virus spread, attract immune cells for eradication, and stimulate angiogenesis, growth, and wound repair after viral damage. Because mammalian and marsupial platelets became smaller and more plate-like their biophysical properties improved in function, which facilitated distribution near vessel walls in fluid-shear fields. This adaptation increased the probability that platelets could then interact with and engulf shedding virus particles. Platelets also generate circulating microvesicles that increase membrane surface-area encounters and mark viral targets. In order to match virus-production rates, billions of platelets are generated and turned over per day to continually provide active defenses and adaptation to suppress the spectrum of evolving threats like SARS-CoV-2. Springer US 2022-01-12 2022 /pmc/articles/PMC8754476/ /pubmed/35022962 http://dx.doi.org/10.1007/s10555-022-10019-5 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Non-Thematic Review
Menter, David G.
Afshar-Kharghan, Vahid
Shen, John Paul
Martch, Stephanie L.
Maitra, Anirban
Kopetz, Scott
Honn, Kenneth V.
Sood, Anil K.
Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
title Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
title_full Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
title_fullStr Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
title_full_unstemmed Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
title_short Of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
title_sort of vascular defense, hemostasis, cancer, and platelet biology: an evolutionary perspective
topic Non-Thematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8754476/
https://www.ncbi.nlm.nih.gov/pubmed/35022962
http://dx.doi.org/10.1007/s10555-022-10019-5
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