Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/180509
Full metadata record
DC FieldValueLanguage
dc.contributor.authorLyu, Zipanen_US
dc.contributor.authorChan, Yau-Tuenen_US
dc.contributor.authorLu, Yuanjunen_US
dc.contributor.authorLam, Tsz Fungen_US
dc.contributor.authorWu, Xingyaoen_US
dc.contributor.authorWu, Junyuen_US
dc.contributor.authorXu, Linen_US
dc.contributor.authorYang, Weien_US
dc.contributor.authorZhang, Chengen_US
dc.contributor.authorZhong, Linda Lidanen_US
dc.contributor.authorWang, Ningen_US
dc.date.accessioned2024-10-09T08:00:35Z-
dc.date.available2024-10-09T08:00:35Z-
dc.date.issued2024-
dc.identifier.citationLyu, Z., Chan, Y., Lu, Y., Lam, T. F., Wu, X., Wu, J., Xu, L., Yang, W., Zhang, C., Zhong, L. L. & Wang, N. (2024). Osteoprotegerin mediates adipogenesis in obesity. Journal of Advanced Research, 62, 245-255. https://dx.doi.org/10.1016/j.jare.2024.06.018en_US
dc.identifier.issn2090-1232en_US
dc.identifier.urihttps://hdl.handle.net/10356/180509-
dc.description.abstractIntroduction: Adipogenesis, the process of white adipose tissue expansion, plays a critical role in the development of obesity. Osteoprotegerin (OPG), known for its role in bone metabolism regulation, emerges as a potential regulator in mediating adipogenesis during obesity onset. Objectives: This study aims to elucidate the involvement of OPG in adipogenesis during the early phases of diet-induced obesity and explore its therapeutic potential in obesity management. Methods: Using a diet-induced obesity model, we investigated OPG expression patterns in adipocytes and explored the mechanisms underlying its involvement in adipogenesis. We also assessed the effects of targeted silencing of OPG and recombinant OPG administration on obesity progression and insulin resistance. Additionally, the impact of electroacupuncture treatment on OPG levels and obesity management was evaluated in both animal models and human participants. Results: OPG expression was prominently activated in adipocytes of white adipose tissues during the early phase of diet-induced obesity. Hyperlipidemia induced Cbfa1-dependent OPG transcription, initiating and promoting adipogenesis, leading to cell-size expansion and lipid storage. Intracellular OPG physically bound to RAR and released the PPARɤ/RXR complex, activating adipogenesis-associated gene expression. Targeted silencing of OPG suppressed obesity development, while recombinant OPG administration promoted disease progression and insulin resistance in obese mice. Electroacupuncture treatment suppressed obesity development in an OPG-dependent manner and improved obesity parameters in obese human participants. Conclusion: OPG emerges as a key regulator in mediating adipogenesis during obesity development. Targeting OPG holds promise for the prevention and treatment of obesity, as evidenced by the efficacy of electroacupuncture treatment in modulating OPG levels and managing obesity-related outcomes.en_US
dc.description.sponsorshipNanyang Technological Universityen_US
dc.language.isoenen_US
dc.relation22387-00001en_US
dc.relation.ispartofJournal of Advanced Researchen_US
dc.rights© 2024 The Authors. Published by Elsevier B.V. on behalf of Cairo 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.subjectMedicine, Health and Life Sciencesen_US
dc.titleOsteoprotegerin mediates adipogenesis in obesityen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.identifier.doi10.1016/j.jare.2024.06.018-
dc.description.versionPublished versionen_US
dc.identifier.pmid38906326-
dc.identifier.scopus2-s2.0-85196944993-
dc.identifier.volume62en_US
dc.identifier.spage245en_US
dc.identifier.epage255en_US
dc.subject.keywordsOsteoprotegerinen_US
dc.subject.keywordsObesityen_US
dc.description.acknowledgementThis work is financially supported by the University Research Committee of The University of Hong Kong (Project Code: 104006600), Nanyang Technological University Research Committee (Project Code: #22387-00001), Research Grant Committee of Hong Kong (Project Code: 17119621), The Health and Medical Research Fund (Project Code: 19201591 and 15162961) and Innovation and Technology Fund (Project Code: PRP/028/22FX), Health and Medical Research Fund (Project Code: 15163331).en_US
item.grantfulltextopen-
item.fulltextWith Fulltext-
Appears in Collections:SBS Journal Articles
Files in This Item:
File Description SizeFormat 
1-s2.0-S2090123224002558-main.pdf3.75 MBAdobe PDFThumbnail
View/Open

SCOPUSTM   
Citations 50

1
Updated on Dec 6, 2024

Page view(s)

58
Updated on Dec 11, 2024

Download(s)

3
Updated on Dec 11, 2024

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.