Mapping Distinct Bone Marrow Niche Populations and Their Differentiation Paths
Author(s) -
Samuel L. Wolock,
Indira Krishnan,
Danielle Tenen,
Victoria Matkins,
Virginia Camacho,
Sweta B. Patel,
Puneet Agarwal,
Ravi Bhatia,
Daniel G. Tenen,
Allon M. Klein,
Robert S. Welner
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.06.031
Subject(s) - bone marrow , biology , stromal cell , haematopoiesis , osteocyte , microbiology and biotechnology , chondrocyte , transcription factor , phenotype , cartilage , mesenchymal stem cell , cellular differentiation , immunology , stem cell , genetics , osteoblast , cancer research , gene , anatomy , in vitro
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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