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LncRNA GACAT2 binds with protein PKM1/2 to regulate cell mitochondrial function and cementogenesis in an inflammatory environment

LncRNA GACAT2 binds with protein PKM1/2 to regulate cell mitochondrial function and cementogenesis in an inflammatory environment

作     者:Xuan Li Bei-Min Tian Dao-Kun Deng Fen Liu Huan Zhou De-Qin Kong Hong-Lei Qu Li-Juan Sun Xiao-Tao He Fa-Ming Chen Xuan Li;Bei-Min Tian;Dao-Kun Deng;Fen Liu;Huan Zhou;De-Qin Kong;Hong-Lei Qu;Li-Juan Sun;Xiao-Tao He;Fa-Ming Chen

作者机构:State Key Laboratory of Military Stomatology&National Clinical Research Center for Oral Diseases&Shaanxi Engineering Research Center for Dental Materials and Advanced ManufactureDepartment of PeriodontologySchool of StomatologyThe Fourth Military Medical UniversityXi’an 710032P.R.China Department of StomatologyNorthwest Women’s and Children’s HospitalXi’an 710032P.R.China Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine ResearchDepartment of PeriodontologyCollege of StomatologyXi’an Jiaotong UniversityXi’an 710032P.R.China Department of ToxicologyShaanxi Provincial Key Laboratory of Free Radical Biology and MedicineThe Ministry of Education Key Laboratory of Hazard Assessment and Control in Special Operational EnvironmentSchool of Public HealthFourth Military Medical UniversityXi’an 710032P.R.China 

出 版 物:《Bone Research》 (骨研究(英文版))

年 卷 期:2022年第10卷第3期

页      面:494-508页

核心收录:

学科分类:0831[工学-生物医学工程(可授工学、理学、医学学位)] 1003[医学-口腔医学] 100302[医学-口腔临床医学] 10[医学] 

基  金:the funding support provided by the National Natural Science Foundation of China(NSFC,Grant Nos.81970947,82001102 and 81800971) the Natural Science Basic Research Program of Shaanxi(Program Nos.2020JQ-447 and 2020JQ-444) 

主  题:inflammation inflammatory impaired 

摘      要:Periodontal ligament stem cells(PDLSCs) are a key cell type for restoring/regenerating lost/damaged periodontal tissues, including alveolar bone, periodontal ligament and root cementum, the latter of which is important for regaining tooth function. However,PDLSCs residing in an inflammatory environment generally exhibit compromised functions, as demonstrated by an impaired ability to differentiate into cementoblasts, which are responsible for regrowing the cementum. This study investigated the role of mitochondrial function and downstream long noncoding RNAs(lnc RNAs) in regulating inflammation-induced changes in the cementogenesis of PDLSCs. We found that the inflammatory cytokine-induced impairment of the cementogenesis of PDLSCs was closely correlated with their mitochondrial function, and lnc RNA microarray analysis and gain/loss-of-function studies identified GACAT2 as a regulator of the cellular events involved in inflammation-mediated mitochondrial function and ***, a comprehensive identification of RNA-binding proteins by mass spectrometry(Ch IRP-MS) and parallel reaction monitoring(PRM) assays revealed that GACAT2 could directly bind to pyruvate kinase M1/2(PKM1/2), a protein correlated with mitochondrial function. Further functional studies demonstrated that GACAT2 overexpression increased the cellular protein expression of PKM1/2, the PKM2 tetramer and phosphorylated PKM2, which led to enhanced pyruvate kinase(PK) activity and increased translocation of PKM2 into mitochondria. We then found that GACAT2 overexpression could reverse the damage to mitochondrial function and cementoblastic differentiation of PDLSCs induced by inflammation and that this effect could be abolished by PKM1/2 knockdown. Our data indicated that by binding to PKM1/2 proteins, the lnc RNA GACAT2 plays a critical role in regulating mitochondrial function and cementogenesis in an inflammatory environment.

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