| Literature DB >> 33839219 |
Daniel Fraher1, Robert J Mann1, Matthew J Dubuisson2, Megan K Ellis1, Tingsheng Yu3, Ken Walder1, Alister C Ward1, Christoph Winkler3, Yann Gibert4.
Abstract
Osteoporosis is an increasing burden on public health as the world-wide population ages and effective therapeutics are severely needed. Two pathways with high potential for osteoporosis treatment are the retinoic acid (RA) and endocannabinoid system (ECS) signaling pathways. We sought to elucidate the roles that these pathways play in bone development and maturation. Here, we use chemical treatments to modulate the RA and ECS pathways at distinct early, intermediate, and late times bone development in zebrafish. We further assessed osteoclast activity later in zebrafish and medaka. Finally, by combining sub-optimal doses of AR and ECS modulators, we show that enhancing RA signaling or reducing the ECS promote bone formation and decrease osteoclast abundance and activity. These data demonstrate that RA signaling and the ECS can be combined as sub-optimal doses to influence bone growth and may be key targets for potential therapeutics.Entities:
Keywords: Endocannabinoid; Medaka; Osteoblast; Osteoclast; Retinoic acid; Zebrafish
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Year: 2021 PMID: 33839219 PMCID: PMC8127411 DOI: 10.1016/j.mce.2021.111267
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.369