| Literature DB >> 33972395 |
Angeliki Vogiatzi1, Ismini Baltsavia1, Emmanuel Dialynas2, Vasiliki Theodorou2, Yan Zhou3, Elena Deligianni2, Ioannis Iliopoulos1, Andrew O M Wilkie3, Stephen R F Twigg3, George Mavrothalassitis1,2.
Abstract
ETS2 repressor factor (ERF) haploinsufficiency causes late-onset craniosynostosis (CRS) (OMIM entry 600775; CRS4) in humans, while in mice Erf insufficiency also leads to a similar multisuture synostosis phenotype preceded by mildly reduced calvarium ossification. However, neither the cell types affected nor the effects per se have been identified so far. Here, we establish an ex vivo system for the expansion of suture-derived mesenchymal stem and progenitor cells (sdMSCs) and analyze the role of Erf levels in their differentiation. Cellular data suggest that Erf insufficiency specifically decreases osteogenic differentiation of sdMSCs, resulting in the initially delayed mineralization of the calvarium. Transcriptome analysis indicates that Erf is required for efficient osteogenic lineage commitment of sdMSCs. Elevated retinoic acid catabolism due to increased levels of the cytochrome P450 superfamily member Cyp26b1 as a result of decreased Erf levels appears to be the underlying mechanism leading to defective differentiation. Exogenous addition of retinoic acid can rescue the osteogenic differentiation defect, suggesting that Erf affects cranial bone mineralization during skull development through retinoic acid gradient regulation.Entities:
Keywords: Ets transcription factors; craniosynostosis; mesenchymal stem cells; retinoic acid
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Year: 2021 PMID: 33972395 PMCID: PMC8300784 DOI: 10.1128/MCB.00149-21
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272