Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/91519
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dc.contributorDepartment of Biomedical Engineering-
dc.creatorXu, J-
dc.creatorHu, P-
dc.creatorZhang, X-
dc.creatorChen, J-
dc.creatorWang, J-
dc.creatorZhang, J-
dc.creatorChen, Z-
dc.creatorYu, MK-
dc.creatorChung, YW-
dc.creatorWang, Y-
dc.creatorZhang, X-
dc.creatorZhang, Y-
dc.creatorZheng, N-
dc.creatorYao, H-
dc.creatorYue, J-
dc.creatorChan, HC-
dc.creatorQin, L-
dc.creatorRuan, YC-
dc.date.accessioned2021-11-03T06:54:20Z-
dc.date.available2021-11-03T06:54:20Z-
dc.identifier.urihttp://hdl.handle.net/10397/91519-
dc.language.isoenen_US
dc.publisherKe Ai Publishing Communications Ltd.en_US
dc.rights© 2021 THE AUTHORS. Published by Elsevier BV on behalf of Faculty of Engineering, Ain Shams University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Xu, J., Hu, P., Zhang, X., Chen, J., Wang, J., Zhang, J., . . . Ruan, Y. C. (2022). Magnesium implantation or supplementation ameliorates bone disorder in CFTR-mutant mice through an ATF4-dependent wnt/β-catenin signaling. Bioactive Materials, 8, 95-108 is available at https://doi.org/10.1016/j.bioactmat.2021.06.034en_US
dc.subjectATF4en_US
dc.subjectCystic fibrosis-related bone disorderen_US
dc.subjectMagnesium implanten_US
dc.subjectWnt signalingen_US
dc.titleMagnesium implantation or supplementation ameliorates bone disorder in CFTR-mutant mice through an ATF4-dependent Wnt/β-catenin signalingen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage95-
dc.identifier.epage108-
dc.identifier.volume8-
dc.identifier.doi10.1016/j.bioactmat.2021.06.034-
dcterms.abstractMagnesium metal and its alloys are being developed as effective orthopedic implants; however, the mechanisms underlying the actions of magnesium on bones remain unclear. Cystic fibrosis, the most common genetic disease in Caucasians caused by the mutation of CFTR, has shown bone disorder as a key clinical manifestation, which currently lacks effective therapeutic options. Here we report that implantation of magnesium-containing implant stimulates bone formation and improves bone fracture healing in CFTR-mutant mice. Wnt/β-catenin signaling in the bone is enhanced by the magnesium implant, and inhibition of Wnt/β-catenin by iCRT14 blocks the magnesium implant to improve fracture healing in CFTR-mutant mice. We further demonstrate that magnesium ion enters osteocytes, increases intracellular cAMP level and activates ATF4, a key transcription factor known to regulate Wnt/β-catenin signaling. In vivo knockdown of ATF4 abolishes the magnesium implant-activated β-catenin in bones and reverses the improved-fracture healing in CFTR-mutant mice. In addition, oral supplementation of magnesium activates ATF4 and β-catenin as well as enhances bone volume and density in CFTR-mutant mice. Together, these results show that magnesium implantation or supplementation may serve as a potential anabolic therapy for cystic fibrosis-related bone disease. Activation of ATF4-dependent Wnt/β-catenin signaling in osteocytes is identified as a previously undefined mechanism underlying the beneficial effect of magnesium on bone formation.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBioactive materials, Feb. 2022, v. 8, p. 95-108-
dcterms.isPartOfBioactive materials-
dcterms.issued2022-02-
dc.identifier.scopus2-s2.0-85109099212-
dc.identifier.eissn2452-199X-
dc.description.validate202110 bcvc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.pubStatusPublisheden_US
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