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Mapping Distinct Bone Marrow Niche Populations and Their Differentiation Paths.
Wolock, Samuel L; Krishnan, Indira; Tenen, Danielle E; Matkins, Victoria; Camacho, Virginia; Patel, Sweta; Agarwal, Puneet; Bhatia, Ravi; Tenen, Daniel G; Klein, Allon M; Welner, Robert S.
Afiliación
  • Wolock SL; Department of System Biology, Harvard Medical School, Boston, MA, USA.
  • Krishnan I; Harvard Stem Cell Institute, Harvard Medical School, Boston, MA, USA.
  • Tenen DE; Division of Endocrinology, Diabetes, and Metabolism, Beth Israel Deaconess Medical Center, Boston, MA, USA.
  • Matkins V; Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Camacho V; Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Patel S; Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Agarwal P; Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Bhatia R; Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Tenen DG; Harvard Stem Cell Institute, Harvard Medical School, Boston, MA, USA; Cancer Science Institute, National University of Singapore, Singapore, Singapore.
  • Klein AM; Department of System Biology, Harvard Medical School, Boston, MA, USA.
  • Welner RS; Division of Hematology/Oncology, University of Alabama at Birmingham, Birmingham, AL, USA. Electronic address: rwelner@uab.edu.
Cell Rep ; 28(2): 302-311.e5, 2019 07 09.
Article en En | MEDLINE | ID: mdl-31291568
ABSTRACT
The bone marrow microenvironment is composed of heterogeneous cell populations of non-hematopoietic cells with complex phenotypes and undefined trajectories of maturation. Among them, mesenchymal cells maintain the production of stromal, bone, fat, and cartilage cells. Resolving these unique cellular subsets within the bone marrow remains challenging. Here, we used single-cell RNA sequencing of non-hematopoietic bone marrow cells to define specific subpopulations. Furthermore, by combining computational prediction of the cell state hierarchy with the known expression of key transcription factors, we mapped differentiation paths to the osteocyte, chondrocyte, and adipocyte lineages. Finally, we validated our findings using lineage-specific reporter strains and targeted knockdowns. Our analysis reveals differentiation hierarchies for maturing stromal cells, determines key transcription factors along these trajectories, and provides an understanding of the complexity of the bone marrow microenvironment.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Médula Ósea / Nicho de Células Madre Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cell Rep Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Médula Ósea / Nicho de Células Madre Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cell Rep Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos