lncRNA Ubr5 promotes BMSCs apoptosis and inhibits their proliferation and osteogenic differentiation in weightless bone loss

Weightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The aim of this study was to systematically investigate the differential expression profiles of mRNAs and long noncoding RNAs (lncRNAs) to explore...

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Published inFrontiers in cell and developmental biology Vol. 13; p. 1543929
Main Authors Wang, Dong, Gao, Yuan, Tan, Yingjun, Li, Na, Li, Xi, Li, Jiaxiang, Pan, Yikai, Zhao, Xingcheng, Yan, Ming, Wang, Yongchun
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LanguageEnglish
Published Switzerland Frontiers Media S.A 02.04.2025
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Abstract Weightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The aim of this study was to systematically investigate the differential expression profiles of mRNAs and long noncoding RNAs (lncRNAs) to explore the molecular pathogenesis underlying weightless bone loss. Transcriptome sequencing was performed on bone marrow mesenchymal stem cell (BMSCs) samples from the Ground control group and simulated microgravity (SMG) group using Illumina technology. Using the DESeq2 algorithm, we accurately identify and analyzed the differentially expressed genes (DEGs). Subsequently, the molecular functions and signaling pathways enriched by DEG were comprehensively analyzed by GO and KEGG. In addition, by constructing lncRNA-mRNA coexpression network, this study screened and verified key lncRNAs as potential genes to further explore their role in the occurrence and development of weightless bone loss. A total of 215 differentially expressed lncRNAs (DElncRNAs) and 381 differentially expressed mRNAs (DEmRNAs) were identified, in the SMG group. DEmRNAs were primarily involved in the cell response to mechanical stimulation, microtubule motility and TNF signaling pathway. Meanwhile, DElncRNAs are significantly enriched in cell differentiation, fatty acid metabolic process and biosynthesis of amino acids. In addition, the expression levels of related lncRNAs and mRNAs in weightless bone loss were verified via qRT-PCR. lncRNA-mRNA coexpression network found that lncRNA Ubr5 closely related to osteoblast proliferation and differentiation. Further experimental results revealed that knocking down lncRNA Ubr5 can promote the apoptosis of BMSCs and inhibit their proliferation and osteogenic differentiation. This study revealed the molecular pathogenesis of weightless bone loss, identified lncRNA Ubr5 as a potential intervention target, and provided an important scientific basis and strategic guidance for the prevention and treatment of weightless bone loss.
AbstractList Weightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The aim of this study was to systematically investigate the differential expression profiles of mRNAs and long noncoding RNAs (lncRNAs) to explore the molecular pathogenesis underlying weightless bone loss.BackgroundWeightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The aim of this study was to systematically investigate the differential expression profiles of mRNAs and long noncoding RNAs (lncRNAs) to explore the molecular pathogenesis underlying weightless bone loss.Transcriptome sequencing was performed on bone marrow mesenchymal stem cell (BMSCs) samples from the Ground control group and simulated microgravity (SMG) group using Illumina technology. Using the DESeq2 algorithm, we accurately identify and analyzed the differentially expressed genes (DEGs). Subsequently, the molecular functions and signaling pathways enriched by DEG were comprehensively analyzed by GO and KEGG. In addition, by constructing lncRNA-mRNA coexpression network, this study screened and verified key lncRNAs as potential genes to further explore their role in the occurrence and development of weightless bone loss.MethodsTranscriptome sequencing was performed on bone marrow mesenchymal stem cell (BMSCs) samples from the Ground control group and simulated microgravity (SMG) group using Illumina technology. Using the DESeq2 algorithm, we accurately identify and analyzed the differentially expressed genes (DEGs). Subsequently, the molecular functions and signaling pathways enriched by DEG were comprehensively analyzed by GO and KEGG. In addition, by constructing lncRNA-mRNA coexpression network, this study screened and verified key lncRNAs as potential genes to further explore their role in the occurrence and development of weightless bone loss.A total of 215 differentially expressed lncRNAs (DElncRNAs) and 381 differentially expressed mRNAs (DEmRNAs) were identified, in the SMG group. DEmRNAs were primarily involved in the cell response to mechanical stimulation, microtubule motility and TNF signaling pathway. Meanwhile, DElncRNAs are significantly enriched in cell differentiation, fatty acid metabolic process and biosynthesis of amino acids. In addition, the expression levels of related lncRNAs and mRNAs in weightless bone loss were verified via qRT-PCR. lncRNA-mRNA coexpression network found that lncRNA Ubr5 closely related to osteoblast proliferation and differentiation. Further experimental results revealed that knocking down lncRNA Ubr5 can promote the apoptosis of BMSCs and inhibit their proliferation and osteogenic differentiation.ResultsA total of 215 differentially expressed lncRNAs (DElncRNAs) and 381 differentially expressed mRNAs (DEmRNAs) were identified, in the SMG group. DEmRNAs were primarily involved in the cell response to mechanical stimulation, microtubule motility and TNF signaling pathway. Meanwhile, DElncRNAs are significantly enriched in cell differentiation, fatty acid metabolic process and biosynthesis of amino acids. In addition, the expression levels of related lncRNAs and mRNAs in weightless bone loss were verified via qRT-PCR. lncRNA-mRNA coexpression network found that lncRNA Ubr5 closely related to osteoblast proliferation and differentiation. Further experimental results revealed that knocking down lncRNA Ubr5 can promote the apoptosis of BMSCs and inhibit their proliferation and osteogenic differentiation.This study revealed the molecular pathogenesis of weightless bone loss, identified lncRNA Ubr5 as a potential intervention target, and provided an important scientific basis and strategic guidance for the prevention and treatment of weightless bone loss.ConclusionThis study revealed the molecular pathogenesis of weightless bone loss, identified lncRNA Ubr5 as a potential intervention target, and provided an important scientific basis and strategic guidance for the prevention and treatment of weightless bone loss.
Weightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The aim of this study was to systematically investigate the differential expression profiles of mRNAs and long noncoding RNAs (lncRNAs) to explore the molecular pathogenesis underlying weightless bone loss. Transcriptome sequencing was performed on bone marrow mesenchymal stem cell (BMSCs) samples from the Ground control group and simulated microgravity (SMG) group using Illumina technology. Using the DESeq2 algorithm, we accurately identify and analyzed the differentially expressed genes (DEGs). Subsequently, the molecular functions and signaling pathways enriched by DEG were comprehensively analyzed by GO and KEGG. In addition, by constructing lncRNA-mRNA coexpression network, this study screened and verified key lncRNAs as potential genes to further explore their role in the occurrence and development of weightless bone loss. A total of 215 differentially expressed lncRNAs (DElncRNAs) and 381 differentially expressed mRNAs (DEmRNAs) were identified, in the SMG group. DEmRNAs were primarily involved in the cell response to mechanical stimulation, microtubule motility and TNF signaling pathway. Meanwhile, DElncRNAs are significantly enriched in cell differentiation, fatty acid metabolic process and biosynthesis of amino acids. In addition, the expression levels of related lncRNAs and mRNAs in weightless bone loss were verified via qRT-PCR. lncRNA-mRNA coexpression network found that lncRNA Ubr5 closely related to osteoblast proliferation and differentiation. Further experimental results revealed that knocking down lncRNA Ubr5 can promote the apoptosis of BMSCs and inhibit their proliferation and osteogenic differentiation. This study revealed the molecular pathogenesis of weightless bone loss, identified lncRNA Ubr5 as a potential intervention target, and provided an important scientific basis and strategic guidance for the prevention and treatment of weightless bone loss.
BackgroundWeightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The aim of this study was to systematically investigate the differential expression profiles of mRNAs and long noncoding RNAs (lncRNAs) to explore the molecular pathogenesis underlying weightless bone loss.MethodsTranscriptome sequencing was performed on bone marrow mesenchymal stem cell (BMSCs) samples from the Ground control group and simulated microgravity (SMG) group using Illumina technology. Using the DESeq2 algorithm, we accurately identify and analyzed the differentially expressed genes (DEGs). Subsequently, the molecular functions and signaling pathways enriched by DEG were comprehensively analyzed by GO and KEGG. In addition, by constructing lncRNA-mRNA coexpression network, this study screened and verified key lncRNAs as potential genes to further explore their role in the occurrence and development of weightless bone loss.ResultsA total of 215 differentially expressed lncRNAs (DElncRNAs) and 381 differentially expressed mRNAs (DEmRNAs) were identified, in the SMG group. DEmRNAs were primarily involved in the cell response to mechanical stimulation, microtubule motility and TNF signaling pathway. Meanwhile, DElncRNAs are significantly enriched in cell differentiation, fatty acid metabolic process and biosynthesis of amino acids. In addition, the expression levels of related lncRNAs and mRNAs in weightless bone loss were verified via qRT-PCR. lncRNA-mRNA coexpression network found that lncRNA Ubr5 closely related to osteoblast proliferation and differentiation. Further experimental results revealed that knocking down lncRNA Ubr5 can promote the apoptosis of BMSCs and inhibit their proliferation and osteogenic differentiation.ConclusionThis study revealed the molecular pathogenesis of weightless bone loss, identified lncRNA Ubr5 as a potential intervention target, and provided an important scientific basis and strategic guidance for the prevention and treatment of weightless bone loss.
Author Gao, Yuan
Wang, Yongchun
Zhao, Xingcheng
Wang, Dong
Pan, Yikai
Li, Jiaxiang
Li, Na
Yan, Ming
Tan, Yingjun
Li, Xi
AuthorAffiliation 3 Department of Orthopedic Surgery , Xijing Hospital , Air Force Medical University , Xi’an , China
2 State Key Laboratory of Space Medicine Fundamentals and Application , China Astronaut Research and Training Center , Beijing , China
1 Department of Aerospace Medical Training , School of Aerospace Medicine , Air Force Medical University , Xi’an , China
AuthorAffiliation_xml – name: 1 Department of Aerospace Medical Training , School of Aerospace Medicine , Air Force Medical University , Xi’an , China
– name: 2 State Key Laboratory of Space Medicine Fundamentals and Application , China Astronaut Research and Training Center , Beijing , China
– name: 3 Department of Orthopedic Surgery , Xijing Hospital , Air Force Medical University , Xi’an , China
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Cites_doi 10.1016/j.abb.2008.03.018
10.1359/JBMR.041105
10.1016/j.prp.2024.155413
10.1302/2046-3758.126.BJR-2022-0324.R1
10.1016/j.bbrc.2015.11.006
10.1002/advs.202303375
10.1242/dev.174045
10.1016/j.resp.2009.07.005
10.1016/j.bone.2017.04.006
10.1038/s41413-022-00191-3
10.1016/j.isci.2023.107042
10.1016/j.ijbiomac.2023.127824
10.1007/s40520-013-0101-2
10.1534/genetics.112.146704
10.1096/fj.201802075R
10.1074/jbc.M110.209817
10.3390/ijms222312885
10.1186/1471-2105-9-559
10.1038/s41419-022-04914-6
10.1016/j.ygeno.2020.09.041
10.1007/s00223-014-9851-x
10.1038/nrg2521
10.1155/2022/5719077
10.1146/annurev-biochem-051410-092902
10.1038/celldisc.2016.15
10.1007/s11914-012-0096-1
10.1111/j.1365-2184.2007.00461.x
10.1016/j.isci.2024.109263
10.1038/s41598-021-03017-0
10.1016/j.patbio.2004.12.005
10.1038/35059243
10.1210/en.2003-1156
10.1002/cac2.12607
10.1016/j.gene.2024.148258
10.1038/s41580-020-00315-9
10.1002/jcb.26230
10.1038/s41413-020-0099-y
10.1007/s13577-023-00888-5
10.1016/s0140-6736(00)02217-0
10.1016/j.devcel.2009.04.008
10.1210/er.2012-1026
10.1016/j.ydbio.2007.05.038
10.1016/j.bone.2007.12.224
10.1038/s41392-023-01630-1
10.1002/jcp.26013
10.18632/aging.203267
10.3389/fcell.2021.647387
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Keywords lncRNA Ubr5
lncRNA-mRNA coexpression network
weightless bone loss
bone marrow mesenchymal stem cells
simulated weightlessness
Language English
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These authors have contributed equally to this work
Pingguo Duan, The First Affiliated Hospital of Nanchang University, China
Edited by: Fan He, Soochow University, China
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References Kung (B19) 2013; 193
Statello (B35) 2021; 22
Karsenty (B17) 2018; 115
Wicik (B43) 2021; 113
Xiang (B45) 2022; 13
Zayzafoon (B46) 2004; 145
Bonewald (B2) 2008; 42
Li (B22); 26
Han (B11) 2021; 13
Sun (B37) 2018; 233
Wloga (B44) 2009; 16
Liu (B26); 260
Zhou (B48) 2021; 11
Hu (B15) 2023; 10
Klein-Nulend (B18) 2005; 53
Dallas (B9) 2013; 34
Liu (B27) 2021; 9
Hou (B13) 2023; 36
Chen (B6) 2015; 468
Langfelder (B20) 2008; 9
Wang (B40) 2022; 2022
Mercer (B29) 2009; 10
Sun (B36) 2016; 2
Smith (B34) 2005; 20
Takata (B38) 2001; 48
Arfat (B1) 2014; 94
Chaimowicz (B5) 2019; 146
Lü (B28) 2019; 33
Iolascon (B16) 2013; 25
Li (B23) 2023; 12
White (B42) 2001; 409
Vico (B39) 2000; 355
Cai (B4) 2024; 44
Dai (B8) 2007; 40
Liu (B24) 2022; 10
Li (B21); 8
Qin (B31) 2020; 8
Gomes (B10) 2021
Liu (B25); 27
Sims (B33) 2012; 10
Zhao (B47) 2024; 254
Hargens (B12) 2009; 169
Rinn (B32) 2012; 81
Coré (B7) 2007; 308
Boyce (B3) 2008; 473
Hu (B14) 2024; 906
Pathak (B30) 2011; 286
Wang (B41) 2018; 119
References_xml – volume: 473
  start-page: 139
  year: 2008
  ident: B3
  article-title: Functions of RANKL/RANK/OPG in bone modeling and remodeling
  publication-title: Arch. Biochem. Biophys.
  doi: 10.1016/j.abb.2008.03.018
– volume: 20
  start-page: 208
  year: 2005
  ident: B34
  article-title: Bone markers, calcium metabolism, and calcium kinetics during extended-duration space flight on the mir space station
  publication-title: J. Bone Min. Res.
  doi: 10.1359/JBMR.041105
– volume: 260
  start-page: 155413
  ident: B26
  article-title: Advances of long non-coding RNAs in osteoclast differentiation and osteoporosis
  publication-title: Pathol. Res. Pract.
  doi: 10.1016/j.prp.2024.155413
– volume: 12
  start-page: 375
  year: 2023
  ident: B23
  article-title: LncRNA PCBP1-AS1 induces osteoporosis by sponging miR-126-5p/PAK2 axis
  publication-title: Bone Jt. Res.
  doi: 10.1302/2046-3758.126.BJR-2022-0324.R1
– volume: 468
  start-page: 21
  year: 2015
  ident: B6
  article-title: Simulated microgravity inhibits osteogenic differentiation of mesenchymal stem cells through down regulating the transcriptional co-activator TAZ
  publication-title: Biochem. Biophys. Res. Commun.
  doi: 10.1016/j.bbrc.2015.11.006
– volume: 10
  start-page: e2303375
  year: 2023
  ident: B15
  article-title: The critical role of the piezo1/β-catenin/ATF4 Axis on the stemness of Gli1(+) BMSCs during simulated microgravity-induced bone loss
  publication-title: Adv. Sci. (Weinh)
  doi: 10.1002/advs.202303375
– volume: 146
  start-page: 146
  year: 2019
  ident: B5
  article-title: Teashirt 1 (Tshz1) is essential for the development, survival and function of hypoglossal and phrenic motor neurons in mouse
  publication-title: Development
  doi: 10.1242/dev.174045
– volume: 169
  start-page: S30
  year: 2009
  ident: B12
  article-title: Cardiovascular adaptations, fluid shifts, and countermeasures related to space flight
  publication-title: Respir. Physiol. Neurobiol.
  doi: 10.1016/j.resp.2009.07.005
– volume: 115
  start-page: 43
  year: 2018
  ident: B17
  article-title: Molecular bases of the crosstalk between bone and muscle
  publication-title: Bone
  doi: 10.1016/j.bone.2017.04.006
– volume: 10
  start-page: 18
  year: 2022
  ident: B24
  article-title: The mechanosensitive lncRNA Neat1 promotes osteoblast function through paraspeckle-dependent Smurf1 mRNA retention
  publication-title: Bone Res.
  doi: 10.1038/s41413-022-00191-3
– volume: 26
  start-page: 107042
  ident: B22
  article-title: SRSF10 regulates proliferation of neural progenitor cells and affects neurogenesis in developing mouse neocortex
  publication-title: Iscience
  doi: 10.1016/j.isci.2023.107042
– volume: 254
  start-page: 127824
  year: 2024
  ident: B47
  article-title: A novel lncRNA GM15416 regulates osteoblast apoptosis and differentiation through the c-Fos/Fas axis and mitigates osteoporosis
  publication-title: Int. J. Biol. Macromol.
  doi: 10.1016/j.ijbiomac.2023.127824
– volume: 25
  start-page: S3
  year: 2013
  ident: B16
  article-title: Mechanobiology of bone
  publication-title: Aging Clin. Exp. Res.
  doi: 10.1007/s40520-013-0101-2
– volume: 193
  start-page: 651
  year: 2013
  ident: B19
  article-title: Long noncoding RNAs: past, present, and future
  publication-title: Genetics
  doi: 10.1534/genetics.112.146704
– volume: 48
  start-page: 147
  year: 2001
  ident: B38
  article-title: Disuse osteoporosis
  publication-title: J. Med. Invest
– volume: 33
  start-page: 4273
  year: 2019
  ident: B28
  article-title: Microgravity-induced hepatogenic differentiation of rBMSCs on board the SJ-10 satellite
  publication-title: Faseb J.
  doi: 10.1096/fj.201802075R
– volume: 286
  start-page: 11685
  year: 2011
  ident: B30
  article-title: Tubulin tyrosine ligase-like genes ttll3 and ttll6 maintain zebrafish cilia structure and motility
  publication-title: J. Biol. Chem.
  doi: 10.1074/jbc.M110.209817
– start-page: 22
  year: 2021
  ident: B10
  article-title: New findings on LMO7 transcripts, proteins and regulatory regions in human and vertebrate model organisms and the intracellular distribution in skeletal muscle cells
  publication-title: Int. J. Mol. Sci.
  doi: 10.3390/ijms222312885
– volume: 9
  start-page: 559
  year: 2008
  ident: B20
  article-title: WGCNA: an R package for weighted correlation network analysis
  publication-title: Bmc Bioinforma.
  doi: 10.1186/1471-2105-9-559
– volume: 13
  start-page: 451
  year: 2022
  ident: B45
  article-title: UBR5 targets tumor suppressor CDC73 proteolytically to promote aggressive breast cancer
  publication-title: Cell Death Dis.
  doi: 10.1038/s41419-022-04914-6
– volume: 113
  start-page: 503
  year: 2021
  ident: B43
  article-title: The crosstalk between bone metabolism, lncRNAs, microRNAs and mRNAs in coronary artery calcification
  publication-title: Genomics
  doi: 10.1016/j.ygeno.2020.09.041
– volume: 94
  start-page: 569
  year: 2014
  ident: B1
  article-title: Physiological effects of microgravity on bone cells
  publication-title: Calcif. Tissue Int.
  doi: 10.1007/s00223-014-9851-x
– volume: 10
  start-page: 155
  year: 2009
  ident: B29
  article-title: Long non-coding RNAs: insights into functions
  publication-title: Nat. Rev. Genet.
  doi: 10.1038/nrg2521
– volume: 2022
  start-page: 5719077
  year: 2022
  ident: B40
  article-title: High-throughput sequencing reveals CXCR4 and IGF1 behave different roles in weightlessness osteoporosis
  publication-title: Stem Cells Int.
  doi: 10.1155/2022/5719077
– volume: 81
  start-page: 145
  year: 2012
  ident: B32
  article-title: Genome regulation by long noncoding RNAs
  publication-title: Annu. Rev. Biochem.
  doi: 10.1146/annurev-biochem-051410-092902
– volume: 2
  start-page: 16015
  year: 2016
  ident: B36
  article-title: Osteoclast-derived microRNA-containing exosomes selectively inhibit osteoblast activity
  publication-title: Cell Discov.
  doi: 10.1038/celldisc.2016.15
– volume: 10
  start-page: 109
  year: 2012
  ident: B33
  article-title: Intercellular cross-talk among bone cells: new factors and pathways
  publication-title: Curr. Osteoporos. Rep.
  doi: 10.1007/s11914-012-0096-1
– volume: 40
  start-page: 671
  year: 2007
  ident: B8
  article-title: Simulated microgravity inhibits the proliferation and osteogenesis of rat bone marrow mesenchymal stem cells
  publication-title: Cell Prolif.
  doi: 10.1111/j.1365-2184.2007.00461.x
– volume: 27
  start-page: 109263
  ident: B25
  article-title: EPC1/2 regulate hematopoietic stem and progenitor cell proliferation by modulating H3 acetylation and DLST
  publication-title: Iscience
  doi: 10.1016/j.isci.2024.109263
– volume: 11
  start-page: 23649
  year: 2021
  ident: B48
  article-title: INTS8 is a therapeutic target for intrahepatic cholangiocarcinoma via the integration of bioinformatics analysis and experimental validation
  publication-title: Sci. Rep.
  doi: 10.1038/s41598-021-03017-0
– volume: 53
  start-page: 576
  year: 2005
  ident: B18
  article-title: Mechanobiology of bone tissue
  publication-title: Pathol. Biol. Paris.
  doi: 10.1016/j.patbio.2004.12.005
– volume: 409
  start-page: 1115
  year: 2001
  ident: B42
  article-title: Humans in space
  publication-title: Nature
  doi: 10.1038/35059243
– volume: 145
  start-page: 2421
  year: 2004
  ident: B46
  article-title: Modeled microgravity inhibits osteogenic differentiation of human mesenchymal stem cells and increases adipogenesis
  publication-title: Endocrinology
  doi: 10.1210/en.2003-1156
– volume: 44
  start-page: 1231
  year: 2024
  ident: B4
  article-title: Targeting SRSF10 might inhibit M2 macrophage polarization and potentiate anti-PD-1 therapy in hepatocellular carcinoma
  publication-title: Cancer Commun. (Lond)
  doi: 10.1002/cac2.12607
– volume: 906
  start-page: 148258
  year: 2024
  ident: B14
  article-title: The role of UBR5 in tumor proliferation and oncotherapy
  publication-title: Gene
  doi: 10.1016/j.gene.2024.148258
– volume: 22
  start-page: 96
  year: 2021
  ident: B35
  article-title: Gene regulation by long non-coding RNAs and its biological functions
  publication-title: Nat. Rev. Mol. Cell Biol.
  doi: 10.1038/s41580-020-00315-9
– volume: 119
  start-page: 669
  year: 2018
  ident: B41
  article-title: Knockdown of lncRNA MEG3 inhibits viability, migration, and invasion and promotes apoptosis by sponging miR-127 in osteosarcoma cell
  publication-title: J. Cell Biochem.
  doi: 10.1002/jcb.26230
– volume: 8
  start-page: 23
  year: 2020
  ident: B31
  article-title: Molecular mechanosensors in osteocytes
  publication-title: Bone Res.
  doi: 10.1038/s41413-020-0099-y
– volume: 36
  start-page: 950
  year: 2023
  ident: B13
  article-title: Long non-coding RNAs in osteoporosis: from mechanisms of action to therapeutic potential
  publication-title: Hum. Cell
  doi: 10.1007/s13577-023-00888-5
– volume: 355
  start-page: 1607
  year: 2000
  ident: B39
  article-title: Effects of long-term microgravity exposure on cancellous and cortical weight-bearing bones of cosmonauts
  publication-title: Lancet
  doi: 10.1016/s0140-6736(00)02217-0
– volume: 16
  start-page: 867
  year: 2009
  ident: B44
  article-title: TTLL3 Is a tubulin glycine ligase that regulates the assembly of cilia
  publication-title: Dev. Cell
  doi: 10.1016/j.devcel.2009.04.008
– volume: 34
  start-page: 658
  year: 2013
  ident: B9
  article-title: The osteocyte: an endocrine cell. and more
  publication-title: Endocr. Rev.
  doi: 10.1210/er.2012-1026
– volume: 308
  start-page: 407
  year: 2007
  ident: B7
  article-title: Tshz1 is required for axial skeleton, soft palate and middle ear development in mice
  publication-title: Dev. Biol.
  doi: 10.1016/j.ydbio.2007.05.038
– volume: 42
  start-page: 606
  year: 2008
  ident: B2
  article-title: Osteocytes, mechanosensing and Wnt signaling
  publication-title: Bone
  doi: 10.1016/j.bone.2007.12.224
– volume: 8
  start-page: 374
  ident: B21
  article-title: Secreted LRPAP1 binds and triggers IFNAR1 degradation to facilitate virus evasion from cellular innate immunity
  publication-title: Signal Transduct. Target Ther.
  doi: 10.1038/s41392-023-01630-1
– volume: 233
  start-page: 1887
  year: 2018
  ident: B37
  article-title: The emerging role of NPNT in tissue injury repair and bone homeostasis
  publication-title: J. Cell Physiol.
  doi: 10.1002/jcp.26013
– volume: 13
  start-page: 18257
  year: 2021
  ident: B11
  article-title: The lncRNA H19/miR-541-3p/Wnt/β-catenin axis plays a vital role in melatonin-mediated osteogenic differentiation of bone marrow mesenchymal stem cells
  publication-title: Aging (Albany Ny)
  doi: 10.18632/aging.203267
– volume: 9
  start-page: 647387
  year: 2021
  ident: B27
  article-title: LMO7 as an unrecognized factor promoting pancreatic cancer progression and metastasis
  publication-title: Front. Cell Dev. Biol.
  doi: 10.3389/fcell.2021.647387
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Snippet Weightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely elucidated. The...
BackgroundWeightless bone loss is a common pathological phenomenon in weightless environments, yet its specific molecular mechanism remain incompletely...
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SubjectTerms bone marrow mesenchymal stem cells
Cell and Developmental Biology
lncRNA Ubr5
lncRNA-mRNA coexpression network
simulated weightlessness
weightless bone loss
Title lncRNA Ubr5 promotes BMSCs apoptosis and inhibits their proliferation and osteogenic differentiation in weightless bone loss
URI https://www.ncbi.nlm.nih.gov/pubmed/40241795
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https://pubmed.ncbi.nlm.nih.gov/PMC11999945
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Volume 13
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