Anucleate platelets generate progeny

Author:

Schwertz Hansjörg12,Köster Sarah34,Kahr Walter H. A.5,Michetti Noemi1,Kraemer Bjoern F.1,Weitz David A.4,Blaylock Robert C.67,Kraiss Larry W.12,Greinacher Andreas8,Zimmerman Guy A.19,Weyrich Andrew S.19

Affiliation:

1. Program in Human Molecular Biology and Genetics and

2. Department of Surgery, University of Utah, Salt Lake City;

3. Department of Nanoscale Imaging of Cellular Dynamics, Courant Research Centre Nano-Spectroscopy and X-Ray Imaging, University of Göttingen, Göttingen, Germany;

4. Department of Physics and Harvard School of Engineering and Applied Sciences, Harvard University, Cambridge, MA;

5. Division of Haematology/Oncology, Program in Cell Biology, Department of Paediatrics, Hospital for Sick Children, University of Toronto, Toronto, ON;

6. ARUP Laboratories and

7. Department of Pathology, University of Utah, Salt Lake City;

8. Institut für Immunologie und Transfusionsmedizin, University of Greifswald, Greifswald, Germany; and

9. Department of Internal Medicine, University of Utah, Salt Lake City

Abstract

Abstract Platelets are classified as terminally differentiated cells that are incapable of cellular division. However, we observe that anucleate human platelets, either maintained in suspension culture or captured in microdrops, give rise to new cell bodies packed with respiring mitochondria and α-granules. Platelet progeny formation also occurs in whole blood cultures. Newly formed platelets are structurally indistinguishable from normal platelets, are able to adhere and spread on extracellular matrix, and display normal signal-dependent expression of surface P-selectin and annexin V. Platelet progeny formation is accompanied by increases in biomass, cellular protein levels, and protein synthesis in expanding populations. Platelet numbers also increase during ex vivo storage. These observations indicate that platelets have a previously unrecognized capacity for producing functional progeny, which involves a form of cell division that does not require a nucleus. Because this new function of platelets occurs outside of the bone marrow milieu, it raises the possibility that thrombopoiesis continues in the bloodstream.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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