Long Non-coding RNA H19 Inhibits Adipocyte Differentiation of Bone Marrow Mesenchymal Stem Cells through Epigenetic Modulation of Histone Deacetylases

被引:139
作者
Huang, Yiping [1 ]
Zheng, Yunfei [1 ]
Jin, Chanyuan [2 ]
Li, Xiaobei [1 ]
Jia, Lingfei [1 ,3 ]
Li, Weiran [1 ,4 ]
机构
[1] Peking Univ, Dept Orthodont, Sch & Hosp Stomatol, Beijing 100081, Peoples R China
[2] Peking Univ, Dept Prosthodont, Sch & Hosp Stomatol, Beijing 100081, Peoples R China
[3] Peking Univ, Cent Lab, Sch & Hosp Stomatol, Beijing 100081, Peoples R China
[4] Beijing Key Lab Digital Stomatol, Natl Engn Lab Digital & Mat Technol Stomatol, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
AGE-RELATED SWITCH; ADIPOGENIC DIFFERENTIATION; DNA METHYLATION; GENE-EXPRESSION; ADIPOSE-TISSUE; GROWTH; CTCF; PROLIFERATION; TRANSCRIPTION; OSTEOPOROSIS;
D O I
10.1038/srep28897
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Bone marrow mesenchymal stem cells (BMSCs) exhibit an increased propensity toward adipocyte differentiation accompanied by a reduction in osteogenesis in osteoporotic bone marrow. However, limited knowledge is available concerning the role of long non-coding RNAs (lncRNAs) in the differentiation of BMSCs into adipocytes. In this study, we demonstrated that lncRNA H19 and microRNA-675 (miR-675) derived from H19 were significantly downregulated in BMSCs that were differentiating into adipocytes. Overexpression of H19 and miR-675 inhibited adipogenesis, while knockdown of their endogenous expression accelerated adipogenic differentiation. Mechanistically, we found that miR-675 targeted the 3' untranslated regions of the histone deacetylase (HDAC) 4-6 transcripts and resulted in deregulation of HDACs 4-6, essential molecules in adipogenesis. In turn, trichostatin A, an HDAC inhibitor, significantly reduced CCCTC-binding factor (CTCF) occupancy in the imprinting control region upstream of the H19 gene locus and subsequently downregulated the expression of H19. These results show that the CTCF/H19/miR-675/HDAC regulatory pathway plays an important role in the commitment of BMSCs into adipocytes.
引用
收藏
页数:13
相关论文
共 46 条
[1]
Long Noncoding RNAs: Cellular Address Codes in Development and Disease [J].
Batista, Pedro J. ;
Chang, Howard Y. .
CELL, 2013, 152 (06) :1298-1307
[2]
Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene [J].
Bell, AC ;
Felsenfeld, G .
NATURE, 2000, 405 (6785) :482-485
[3]
Mesenchymal stem cells: Revisiting history, concepts, and assays [J].
Bianco, Paolo ;
Robey, Pamela Gehron ;
Simmons, Paul J. .
CELL STEM CELL, 2008, 2 (04) :313-319
[4]
The imprinted H19 noncoding RNA is a primary microRNA precursor [J].
Cai, Xuezhong ;
Cullen, Bryan R. .
RNA, 2007, 13 (03) :313-316
[5]
Long Non-Coding RNA NEAT1 Associates with SRp40 to Temporally Regulate PPARγ2 Splicing during Adipogenesis in 3T3-L1 Cells [J].
Cooper, Denise R. ;
Carter, Gay ;
Li, Pengfei ;
Patel, Rehka ;
Watson, James E. ;
Patel, Niketa A. .
GENES, 2014, 5 (04) :1050-1063
[6]
The H19 long noncoding RNA gives rise to microRNAs miR-675-3p and miR-675-5p to promote skeletal muscle differentiation and regeneration [J].
Dey, Bijan K. ;
Pfeifer, Karl ;
Dutta, Anindya .
GENES & DEVELOPMENT, 2014, 28 (05) :491-501
[7]
The H19 locus: Role of an imprinted non-coding RNA in growth and development [J].
Gabory, Anne ;
Jammes, Helene ;
Dandolo, Luisa .
BIOESSAYS, 2010, 32 (06) :473-480
[8]
FABP4 Attenuates PPARγ and Adipogenesis and Is Inversely Correlated With PPARg in Adipose Tissues [J].
Garin-Shkolnik, Tali ;
Rudich, Assaf ;
Hotamisligil, Goekhan S. ;
Rubinstein, Menachem .
DIABETES, 2014, 63 (03) :900-911
[9]
Georgiou KR, 2012, AM J STEM CELLS, V1, P205
[10]
Relationship between DNA methylation, histone H4 acetylation and gene expression in the mouse imprinted Igf2-H19 domain [J].
Grandjean, V ;
O'Neill, L ;
Sado, T ;
Turner, B ;
Ferguson-Smith, A .
FEBS LETTERS, 2001, 488 (03) :165-169