Mouse multipotent progenitor 5 cells are located at the interphase between hematopoietic stem and progenitor cells

Author:

Sommerkamp Pia123,Romero-Mulero Mari Carmen4ORCID,Narr Andreas123,Ladel Luisa12,Hustin Lucie5ORCID,Schönberger Katharina4,Renders Simon126ORCID,Altamura Sandro7,Zeisberger Petra12,Jäcklein Karin4,Klimmeck Daniel12,Rodriguez-Fraticelli Alejo89ORCID,Camargo Fernando D.910,Perié Leïla5ORCID,Trumpp Andreas1211,Cabezas-Wallscheid Nina412

Affiliation:

1. Division of Stem Cells and Cancer, German Cancer Research Center (DKFZ)–Center for Molecular Biology of Heidelberg University (ZMBH) Alliance, Heidelberg, Germany;

2. Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM gGmbH), Heidelberg, Germany;

3. Faculty of Biosciences, Heidelberg University, Heidelberg, Germany;

4. Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany;

5. Laboratoire Physico Chimie Curie, Institut Curie/Université Paris Sciences & Lettres (PSL)/Sorbonne Université/Centre National de la Recherche Scientifique (CNRS) Unité Mixte de Recherche (UMR) 168, Paris, France;

6. Department of Internal Medicine V, Heidelberg University Hospital, Heidelberg, Germany;

7. Department of Pediatric Hematology, Oncology and Immunology, Heidelberg University Medical Center, Heidelberg, Germany;

8. Department of Pediatrics, Harvard Medical School, Boston, MA;

9. Stem Cell Program, Boston Children’s Hospital, Boston, MA;

10. Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA;

11. German Cancer Consortium (DKTK), Heidelberg, Germany; and

12. Centre for Integrative Biological Signaling Studies (CIBSS), Freiburg, Germany

Abstract

Abstract Hematopoietic stem cells (HSCs) and distinct multipotent progenitor (MPP) populations (MPP1-4) contained within the Lin−Sca-1+c-Kit+ (LSK) compartment have previously been identified using diverse surface-marker panels. Here, we phenotypically define and functionally characterize MPP5 (LSK CD34+CD135−CD48−CD150−). Upon transplantation, MPP5 supports initial emergency myelopoiesis followed by stable contribution to the lymphoid lineage. MPP5, capable of generating MPP1-4 but not HSCs, represents a dynamic and versatile component of the MPP network. To characterize all hematopoietic stem and progenitor cells, we performed RNA-sequencing (RNA-seq) analysis to identify specific transcriptomic landscapes of HSCs and MPP1-5. This was complemented by single-cell RNA-seq analysis of LSK cells to establish the differentiation trajectories from HSCs to MPP1-5. In agreement with functional reconstitution activity, MPP5 is located immediately downstream of HSCs but upstream of the more committed MPP2-4. This study provides a comprehensive analysis of the LSK compartment, focusing on the functional and molecular characteristics of the newly defined MPP5 subset.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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