| Literature DB >> 30602070 |
Yu Usami1,2, Aruni T Gunawardena2, Noelle B Francois2, Satoru Otsuru3,4, Hajime Takano2, Katsutoshi Hirose1, Masatake Matsuoka4, Akiko Suzuki4, Jiahui Huang5, Ling Qin6, Masahiro Iwamoto2,4, Wentian Yang5, Satoru Toyosawa1, Motomi Enomoto-Iwamoto2,4.
Abstract
Active cell proliferation and turnover in the growth plate is essential for embryonic and postnatal bone growth. We performed a lineage tracing of Wnt/β-catenin signaling responsive cells (Wnt-responsive cells) using Axin2CreERT2 ;Rosa26ZsGreen mice and found a novel cell population that resides in the outermost layer of the growth plate facing the Ranvier's groove (RG; the perichondrium adjacent to growth plate). These Wnt-responsive cells rapidly expanded and contributed to formation of the outer growth plate from the neonatal to the growing stage but stopped expanding at the young adult stage when bone longitudinal growth ceases. In addition, a second Wnt-responsive sporadic cell population was localized within the resting zone of the central part of the growth plate during the postnatal growth phase. While it induced ectopic chondrogenesis in the RG, ablation of β-catenin in the Wnt-responsive cells strongly inhibited expansion of their descendants toward the growth plate. These findings indicate that the Wnt-responsive cell population in the outermost layer of the growth plate is a unique cell source of chondroprogenitors involving lateral growth of the growth plate and suggest that Wnt/β-catenin signaling regulates function of skeletal progenitors in a site- and stage-specific manner.Entities:
Keywords: CHONDROCYTE AND CARTILAGE BIOLOGY; GENETIC ANIMAL MODELS; GROWTH PLATE; WNT/β-CATENIN/LRPs
Mesh:
Year: 2019 PMID: 30602070 PMCID: PMC6536347 DOI: 10.1002/jbmr.3658
Source DB: PubMed Journal: J Bone Miner Res ISSN: 0884-0431 Impact factor: 6.741