Alternative splicing in mesenchymal stem cell differentiation

被引:35
作者
Park, Jung Woo [1 ,2 ]
Fu, Siyi [1 ,2 ]
Huang, Borong [1 ,2 ]
Xu, Ren-He [1 ,2 ]
机构
[1] Univ Macau, Ctr Reprod Dev & Aging, Fac Hlth Sci, Macau, Peoples R China
[2] Univ Macau, Inst Translat Med, Fac Hlth Sci, Macau, Peoples R China
关键词
adipogenic; alternative splicing; chondrogenic; ESC differentiation; mesenchymal stem cells; MSC differentiation; neural differentiation; osteogenic; RNA-binding proteins; MESSENGER-RNA; ISOFORM EXPRESSION; TRANSCRIPTION; PROTEIN; ROLES; SOX9; GENE; CHONDROGENESIS; IDENTIFICATION; REGULATOR;
D O I
10.1002/stem.3248
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The differentiation and maturation of mesenchymal stem cells (MSCs) to mesodermal and other lineages are known to be controlled by various extrinsic and intrinsic signals. The dysregulation of the MSC differentiation balance has been linked to several pathophysiological conditions, including obesity and osteoporosis. Previous research of the molecular mechanisms governing MSC differentiation has mostly focused on transcriptional regulation. However, recent findings are revealing the underrated role of alternative splicing (AS) in MSC differentiation and functions. In this review, we discuss recent progress in elucidating the regulatory roles of AS in MSC differentiation. We catalogue and highlight the key AS events that modulate MSC differentiation to major osteocytes, chondrocytes, and adipocytes, and discuss the regulatory mechanisms by which AS is regulated.
引用
收藏
页码:1229 / 1240
页数:12
相关论文
共 92 条
[1]  
Akiyama H, 2002, J BONE MINER RES, V17, pS142
[2]   Key transcription factors in the differentiation of mesenchymal stem cells [J].
Almalki, Sami G. ;
Agrawal, Devendra K. .
DIFFERENTIATION, 2016, 92 (1-2) :41-51
[3]   PPARγΔ5, a Naturally Occurring Dominant-Negative Splice Isoform, Impairs PPARγ Function and Adipocyte Differentiation [J].
Aprile, Marianna ;
Cataldi, Simona ;
Ambrosio, Maria Rosaria ;
D'Esposito, Vittoria ;
Lim, Koini ;
Dietrich, Arne ;
Blueher, Matthias ;
Savage, David Bousfield ;
Formisano, Pietro ;
Ciccodicola, Alfredo ;
Costa, Valerio .
CELL REPORTS, 2018, 25 (06) :1577-+
[4]   Alternative splicing as a regulator of development and tissue identity [J].
Baralle, Francisco E. ;
Giudice, Jimena .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2017, 18 (07) :437-451
[5]   The Evolutionary Landscape of Alternative Splicing in Vertebrate Species [J].
Barbosa-Morais, Nuno L. ;
Irimia, Manuel ;
Pan, Qun ;
Xiong, Hui Y. ;
Gueroussov, Serge ;
Lee, Leo J. ;
Slobodeniuc, Valentina ;
Kutter, Claudia ;
Watt, Stephen ;
Colak, Recep ;
Kim, TaeHyung ;
Misquitta-Ali, Christine M. ;
Wilson, Michael D. ;
Kim, Philip M. ;
Odom, Duncan T. ;
Frey, Brendan J. ;
Blencowe, Benjamin J. .
SCIENCE, 2012, 338 (6114) :1587-1593
[6]   S6K1 Alternative Splicing Modulates Its Oncogenic Activity and Regulates mTORC1 [J].
Ben-Hur, Vered ;
Denichenko, Polina ;
Siegfried, Zahava ;
Maimon, Avi ;
Krainer, Adrian ;
Davidson, Ben ;
Karni, Rotem .
CELL REPORTS, 2013, 3 (01) :103-115
[7]   "Mesenchymal" Stem Cells [J].
Bianco, Paolo .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 30, 2014, 30 :677-704
[8]   Disrupted alternative splicing for genes implicated in splicing and ciliogenesis causes PRPF31 retinitis pigmentosa [J].
Buskin, Adriana ;
Zhu, Lili ;
Chichagova, Valeria ;
Basu, Basudha ;
Mozaffari-Jovin, Sina ;
Dolan, David ;
Droop, Alastair ;
Collin, Joseph ;
Bronstein, Revital ;
Mehrotra, Sudeep ;
Farkas, Michael ;
Hilgen, Gerrit ;
White, Kathryn ;
Pan, Kuan-Ting ;
Treumann, Achim ;
Hallam, Dean ;
Bialas, Katarzyna ;
Chung, Git ;
Mellough, Carla ;
Ding, Yuchun ;
Krasnogor, Natalio ;
Przyborski, Stefan ;
Zwolinski, Simon ;
Al-Aama, Jumana ;
Alharthi, Sameer ;
Xu, Yaobo ;
Wheway, Gabrielle ;
Szymanska, Katarzyna ;
McKibbin, Martin ;
Inglehearn, Chris F. ;
Elliott, David J. ;
Lindsay, Susan ;
Ali, Robin R. ;
Steel, David H. ;
Armstrong, Lyle ;
Sernagor, Evelyne ;
Urlaub, Henning ;
Pierce, Eric ;
Luehrmann, Reinhard ;
Grellscheid, Sushma-Nagaraja ;
Johnson, Colin A. ;
Lako, Majlinda .
NATURE COMMUNICATIONS, 2018, 9
[9]   Modulation of PKM alternative splicing by PTBP1 promotes gemcitabine resistance in pancreatic cancer cells [J].
Calabretta, S. ;
Bielli, P. ;
Passacantilli, I. ;
Pilozzi, E. ;
Fendrich, V. ;
Capurso, G. ;
Delle Fave, G. ;
Sette, C. .
ONCOGENE, 2016, 35 (16) :2031-2039
[10]   MSCs: they work, so use them [J].
Caplan, Arnold I. .
NATURE, 2019, 566 (7742) :39-39