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Identification and Specification of the Mouse Skeletal Stem Cell
Author(s) -
Charles K. F. Chan,
Eun Young Seo,
James Y. Chen,
David Lo,
Adrian McArdle,
Rahul Sinha,
Ruth Tevlin,
Jun Seita,
Justin Vincent-Tompkins,
Taylor Wearda,
Wan-Jin Lu,
Kshemendra Senarath-Yapa,
Michael T. Chung,
Owen Marecic,
Misha C. Tran,
Kelley S. Yan,
Rosalynd Upton,
Graham G. Walmsley,
Andrew S. Lee,
Debashis Sahoo,
Calvin J. Kuo,
Irving L. Weissman,
Michael T. Longaker
Publication year - 2015
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.12.002
Subject(s) - biology , stem cell , identification (biology) , computational biology , microbiology and biotechnology , genetics , evolutionary biology , ecology
How are skeletal tissues derived from skeletal stem cells? Here, we map bone, cartilage, and stromal development from a population of highly pure, postnatal skeletal stem cells (mouse skeletal stem cells, mSSCs) to their downstream progenitors of bone, cartilage, and stromal tissue. We then investigated the transcriptome of the stem/progenitor cells for unique gene-expression patterns that would indicate potential regulators of mSSC lineage commitment. We demonstrate that mSSC niche factors can be potent inducers of osteogenesis, and several specific combinations of recombinant mSSC niche factors can activate mSSC genetic programs in situ, even in nonskeletal tissues, resulting in de novo formation of cartilage or bone and bone marrow stroma. Inducing mSSC formation with soluble factors and subsequently regulating the mSSC niche to specify its differentiation toward bone, cartilage, or stromal cells could represent a paradigm shift in the therapeutic regeneration of skeletal tissues.

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