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...

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Veröffentlicht in:The Journal of experimental medicine 2020-09, Vol.217 (9)
Hauptverfasser: 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
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container_issue 9
container_start_page
container_title The Journal of experimental medicine
container_volume 217
creator 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
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.
doi_str_mv 10.1084/jem.20191206
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subjects Animals
Blood Platelets - cytology
Blood Platelets - metabolism
Blood Platelets - ultrastructure
Bone Marrow Cells - cytology
Cell Lineage
Cell Membrane - metabolism
Cell Membrane - ultrastructure
Databases as Topic
Embryo, Mammalian - cytology
Fetus - cytology
Gene Expression Regulation
Hematopoiesis
Imaging, Three-Dimensional
Integrases - metabolism
Liver - embryology
Megakaryocytes - cytology
Megakaryocytes - metabolism
Mice, Inbred C57BL
Ploidies
Reproducibility of Results
Skull - cytology
title Membrane budding is a major mechanism of in vivo platelet biogenesis
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