From Hematopoietic Stem Cells to Platelets: Unifying Differentiation Pathways Identified by Lineage Tracing Mouse Models

Author:

Manso Bryce A.12ORCID,Rodriguez y Baena Alessandra13ORCID,Forsberg E. Camilla12ORCID

Affiliation:

1. Institute for the Biology of Stem Cells, University of California-Santa Cruz, Santa Cruz, CA 95064, USA

2. Department of Biomolecular Engineering, University of California-Santa Cruz, Santa Cruz, CA 95064, USA

3. Program in Biomedical Sciences and Engineering, Department of Molecular, Cell, and Developmental Biology, University of California-Santa Cruz, Santa Cruz, CA 95064, USA

Abstract

Platelets are the terminal progeny of megakaryocytes, primarily produced in the bone marrow, and play critical roles in blood homeostasis, clotting, and wound healing. Traditionally, megakaryocytes and platelets are thought to arise from multipotent hematopoietic stem cells (HSCs) via multiple discrete progenitor populations with successive, lineage-restricting differentiation steps. However, this view has recently been challenged by studies suggesting that (1) some HSC clones are biased and/or restricted to the platelet lineage, (2) not all platelet generation follows the “canonical” megakaryocytic differentiation path of hematopoiesis, and (3) platelet output is the default program of steady-state hematopoiesis. Here, we specifically investigate the evidence that in vivo lineage tracing studies provide for the route(s) of platelet generation and investigate the involvement of various intermediate progenitor cell populations. We further identify the challenges that need to be overcome that are required to determine the presence, role, and kinetics of these possible alternate pathways.

Funder

National Institutes of Health (NIH) National Institute of General Medical Sciences (NIGMS) Institutional Research and Academic Career Development Awards

Tobacco-Related Disease Research Program

NIH National Institute on Aging

California Institute for Regenerative Medicine

Publisher

MDPI AG

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