Hox11 expressing regional skeletal stem cells are progenitors for osteoblasts, chondrocytes and adipocytes throughout life

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Kyriel M. Pineault
Jane Y. Song
Kenneth M. Kozloff
Daniel Lucas
Deneen M. Wellik
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[1] University of Wisconsin-Madison,Department of Cell & Regenerative Biology
[2] University of Michigan,Cellular and Molecular Biology Program
[3] University of Michigan,Department of Orthopedic Surgery
[4] Cincinnati Children’s Medical Center,Division of Experimental Hematology and Cancer Research
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Multipotent mesenchymal stromal cells (MSCs) are required for skeletal formation, maintenance, and repair throughout life; however, current models posit that postnatally arising long-lived adult MSCs replace transient embryonic progenitor populations. We previously reported exclusive expression and function of the embryonic patterning transcription factor, Hoxa11, in adult skeletal progenitor-enriched MSCs. Here, using a newly generated Hoxa11-CreERT2 lineage-tracing system, we show Hoxa11-lineage marked cells give rise to all skeletal lineages throughout the life of the animal and persist as MSCs. Hoxa11 lineage-positive cells give rise to previously described progenitor-enriched MSC populations marked by LepR-Cre and Osx-CreER, placing them upstream of these populations. Our studies establish that Hox-expressing cells are skeletal stem cells that arise from the earliest stages of skeletal development and self-renew throughout the life of the animal.
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