Hox11 expressing regional skeletal stem cells are progenitors for osteoblasts, chondrocytes and adipocytes throughout life.
Kyriel M PineaultJane Y SongKenneth M KozloffDaniel LucasDeneen M WellikPublished in: Nature communications (2019)
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.
Keyphrases
- stem cells
- induced apoptosis
- mesenchymal stem cells
- long non coding rna
- cell cycle arrest
- cell fate
- transcription factor
- poor prognosis
- endoplasmic reticulum stress
- oxidative stress
- umbilical cord
- single cell
- signaling pathway
- type diabetes
- metabolic syndrome
- cell therapy
- cell proliferation
- young adults
- blood brain barrier
- binding protein
- wild type