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Membrane budding is a major mechanism of in vivo platelet biogenesis
How platelets are produced by megakaryocytes in vivo remains controversial despite more than a century of investigation. Megakaryocytes readily produce proplatelet structures in vitro; however, visualization of platelet release from proplatelets in vivo has remained elusive. We show that within the...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478734/ https://www.ncbi.nlm.nih.gov/pubmed/32706855 http://dx.doi.org/10.1084/jem.20191206 |
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author | Potts, Kathryn S. Farley, Alison Dawson, Caleb A. Rimes, Joel Biben, Christine de Graaf, Carolyn Potts, Margaret A. Stonehouse, Olivia J. Carmagnac, Amandine Gangatirkar, Pradnya Josefsson, Emma C. Anttila, Casey Amann-Zalcenstein, Daniela Naik, Shalin Alexander, Warren S. Hilton, Douglas J. Hawkins, Edwin D. Taoudi, Samir |
author_facet | Potts, Kathryn S. Farley, Alison Dawson, Caleb A. Rimes, Joel Biben, Christine de Graaf, Carolyn Potts, Margaret A. Stonehouse, Olivia J. Carmagnac, Amandine Gangatirkar, Pradnya Josefsson, Emma C. Anttila, Casey Amann-Zalcenstein, Daniela Naik, Shalin Alexander, Warren S. Hilton, Douglas J. Hawkins, Edwin D. Taoudi, Samir |
author_sort | Potts, Kathryn S. |
collection | PubMed |
description | How platelets are produced by megakaryocytes in vivo remains controversial despite more than a century of investigation. Megakaryocytes readily produce proplatelet structures in vitro; however, visualization of platelet release from proplatelets in vivo has remained elusive. We show that within the native prenatal and adult environments, the frequency and rate of proplatelet formation is incompatible with the physiological demands of platelet replacement. We resolve this inconsistency by performing in-depth analysis of plasma membrane budding, a cellular process that has previously been dismissed as a source of platelet production. Our studies demonstrate that membrane budding results in the sustained release of platelets directly into the peripheral circulation during both fetal and adult life without induction of cell death or proplatelet formation. In support of this model, we demonstrate that in mice deficient for NF-E2 (the thrombopoietic master regulator), the absence of membrane budding correlates with failure of in vivo platelet production. Accordingly, we propose that membrane budding, rather than proplatelet formation, supplies the majority of the platelet biomass. |
format | Online Article Text |
id | pubmed-7478734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74787342021-03-07 Membrane budding is a major mechanism of in vivo platelet biogenesis Potts, Kathryn S. Farley, Alison Dawson, Caleb A. Rimes, Joel Biben, Christine de Graaf, Carolyn Potts, Margaret A. Stonehouse, Olivia J. Carmagnac, Amandine Gangatirkar, Pradnya Josefsson, Emma C. Anttila, Casey Amann-Zalcenstein, Daniela Naik, Shalin Alexander, Warren S. Hilton, Douglas J. Hawkins, Edwin D. Taoudi, Samir J Exp Med Article How platelets are produced by megakaryocytes in vivo remains controversial despite more than a century of investigation. Megakaryocytes readily produce proplatelet structures in vitro; however, visualization of platelet release from proplatelets in vivo has remained elusive. We show that within the native prenatal and adult environments, the frequency and rate of proplatelet formation is incompatible with the physiological demands of platelet replacement. We resolve this inconsistency by performing in-depth analysis of plasma membrane budding, a cellular process that has previously been dismissed as a source of platelet production. Our studies demonstrate that membrane budding results in the sustained release of platelets directly into the peripheral circulation during both fetal and adult life without induction of cell death or proplatelet formation. In support of this model, we demonstrate that in mice deficient for NF-E2 (the thrombopoietic master regulator), the absence of membrane budding correlates with failure of in vivo platelet production. Accordingly, we propose that membrane budding, rather than proplatelet formation, supplies the majority of the platelet biomass. Rockefeller University Press 2020-07-24 /pmc/articles/PMC7478734/ /pubmed/32706855 http://dx.doi.org/10.1084/jem.20191206 Text en © 2020 Potts et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Potts, Kathryn S. Farley, Alison Dawson, Caleb A. Rimes, Joel Biben, Christine de Graaf, Carolyn Potts, Margaret A. Stonehouse, Olivia J. Carmagnac, Amandine Gangatirkar, Pradnya Josefsson, Emma C. Anttila, Casey Amann-Zalcenstein, Daniela Naik, Shalin Alexander, Warren S. Hilton, Douglas J. Hawkins, Edwin D. Taoudi, Samir Membrane budding is a major mechanism of in vivo platelet biogenesis |
title | Membrane budding is a major mechanism of in vivo platelet biogenesis |
title_full | Membrane budding is a major mechanism of in vivo platelet biogenesis |
title_fullStr | Membrane budding is a major mechanism of in vivo platelet biogenesis |
title_full_unstemmed | Membrane budding is a major mechanism of in vivo platelet biogenesis |
title_short | Membrane budding is a major mechanism of in vivo platelet biogenesis |
title_sort | membrane budding is a major mechanism of in vivo platelet biogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478734/ https://www.ncbi.nlm.nih.gov/pubmed/32706855 http://dx.doi.org/10.1084/jem.20191206 |
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