Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784632280089624576 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8754476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT menterdavidg ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT afsharkharghanvahid ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT shenjohnpaul ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT martchstephaniel ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT maitraanirban ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT kopetzscott ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT honnkennethv ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective AT soodanilk ofvasculardefensehemostasiscancerandplateletbiologyanevolutionaryperspective |