Alternative platelet differentiation pathways initiated by nonhierarchically related hematopoietic stem cells

Joana Carrelha(University of Oxford), Stefania Mazzi(Karolinska Institutet), Axel Winroth(Karolinska Institutet), Michael Hagemann-Jensen(Karolinska Institutet), Christoph Ziegenhain(Science for Life Laboratory), Kari Högstrand(Karolinska Institutet), Masafumi Seki(Karolinska Institutet), Margs S. Brennan(Karolinska Institutet), Madeleine Lehander(Karolinska Institutet), Bishan Wu(University of Oxford), Yiran Meng(University of Oxford), Ellen Markljung(Karolinska Institutet), Ruggiero Norfo(University of Modena and Reggio Emilia), Hisashi Ishida(Karolinska Institutet), Karin Belander Strålin(Karolinska University Hospital), Francesca Grasso(Karolinska Institutet), Christina Simoglou Karali(University of Oxford), Affaf Aliouat(University of Oxford), Amy Hillen(Karolinska Institutet), Edwin Chari(Karolinska Institutet), Kimberly Siletti(Karolinska Institutet), Supat Thongjuea(University of Oxford), Adam J. Mead(Churchill Hospital), Sten Linnarsson(Karolinska Institutet), Claus Nerlov(University of Oxford), Rickard Sandberg(Karolinska Institutet), Tetsuichi Yoshizato(Karolinska Institutet), Petter Woll(Karolinska Institutet), Sten Eirik W. Jacobsen(Karolinska University Hospital)
Nature Immunology
May 30, 2024
Cited by 37Open Access
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Abstract

Rare multipotent stem cells replenish millions of blood cells per second through a time-consuming process, passing through multiple stages of increasingly lineage-restricted progenitors. Although insults to the blood-forming system highlight the need for more rapid blood replenishment from stem cells, established models of hematopoiesis implicate only one mandatory differentiation pathway for each blood cell lineage. Here, we establish a nonhierarchical relationship between distinct stem cells that replenish all blood cell lineages and stem cells that replenish almost exclusively platelets, a lineage essential for hemostasis and with important roles in both the innate and adaptive immune systems. These distinct stem cells use cellularly, molecularly and functionally separate pathways for the replenishment of molecularly distinct megakaryocyte-restricted progenitors: a slower steady-state multipotent pathway and a fast-track emergency-activated platelet-restricted pathway. These findings provide a framework for enhancing platelet replenishment in settings in which slow recovery of platelets remains a major clinical challenge.


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