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.Jacobsen and colleagues elucidate the nonhierarchical relationship between two types of stem cells: Vwf - hematopoietic stem cells that stably replenish all blood cell lineages without a platelet bias, and Vwf + stem cells that replenish almost exclusively platelets, and demonstrate that the two types utilize cellularly and molecularly distinct progenitor trajectories for replenishment of platelets.

Alternative platelet differentiation pathways initiated by nonhierarchically related hematopoietic stem cells / Carrelha, J.; Mazzi, S.; Winroth, A.; Hagemann-Jensen, M.; Ziegenhain, C.; Högstrand, K.; Seki, M.; Brennan, M. S.; Lehander, M.; Wu, B.; Meng, Y.; Markljung, E.; Norfo, R.; Ishida, H.; Belander Strålin, K.; Grasso, F.; Simoglou Karali, C.; Aliouat, A.; Hillen, A.; Chari, E.; Siletti, K.; Thongjuea, S.; Mead, A. J.; Linnarsson, S.; Nerlov, C.; Sandberg, R.; Yoshizato, T.; Woll, P. S.; Jacobsen, S. E. W.. - In: NATURE IMMUNOLOGY. - ISSN 1529-2908. - 25:6(2024), pp. 1007-1019. [10.1038/s41590-024-01845-6]

Alternative platelet differentiation pathways initiated by nonhierarchically related hematopoietic stem cells

Norfo R.;
2024

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.Jacobsen and colleagues elucidate the nonhierarchical relationship between two types of stem cells: Vwf - hematopoietic stem cells that stably replenish all blood cell lineages without a platelet bias, and Vwf + stem cells that replenish almost exclusively platelets, and demonstrate that the two types utilize cellularly and molecularly distinct progenitor trajectories for replenishment of platelets.
2024
25
6
1007
1019
Alternative platelet differentiation pathways initiated by nonhierarchically related hematopoietic stem cells / Carrelha, J.; Mazzi, S.; Winroth, A.; Hagemann-Jensen, M.; Ziegenhain, C.; Högstrand, K.; Seki, M.; Brennan, M. S.; Lehander, M.; Wu, B.; Meng, Y.; Markljung, E.; Norfo, R.; Ishida, H.; Belander Strålin, K.; Grasso, F.; Simoglou Karali, C.; Aliouat, A.; Hillen, A.; Chari, E.; Siletti, K.; Thongjuea, S.; Mead, A. J.; Linnarsson, S.; Nerlov, C.; Sandberg, R.; Yoshizato, T.; Woll, P. S.; Jacobsen, S. E. W.. - In: NATURE IMMUNOLOGY. - ISSN 1529-2908. - 25:6(2024), pp. 1007-1019. [10.1038/s41590-024-01845-6]
Carrelha, J.; Mazzi, S.; Winroth, A.; Hagemann-Jensen, M.; Ziegenhain, C.; Högstrand, K.; Seki, M.; Brennan, M. S.; Lehander, M.; Wu, B.; Meng, Y.; Ma...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1353588
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