Fusion of Reprogramming Factors Alters the Trajectory of Somatic Lineage Conversion

被引:23
|
作者
Velychko, Sergiy [1 ]
Kang, Kyuree [2 ]
Kim, Sung Min [2 ]
Kwak, Tae Hwan [2 ]
Kim, Kee-Pyo [1 ]
Park, Chanhyeok [3 ]
Hong, Kwonho [3 ]
Chung, ChiHye [4 ]
Hyun, Jung Keun [5 ]
MacCarthy, Caitlin M. [1 ]
Wu, Guangming [1 ]
Schoeler, Hans R. [1 ,2 ]
Han, Dong Wook [2 ,6 ,7 ]
机构
[1] Max Planck Inst Mol Biomed, Dept Cell & Dev Biol, D-48149 Munster, Germany
[2] Konkuk Univ, Sch Med, Dept Stem Cell Biol, 120 Neungdong Ro, Seoul 05029, South Korea
[3] Konkuk Univ, Dept Stem Cell & Regenerat Biotechnol, 120 Neungdong Ro, Seoul 05029, South Korea
[4] Konkuk Univ, Dept Biol Sci, Seoul 05029, South Korea
[5] Dankook Univ, Dept Nanobiomed Sci, Cheonan 330714, South Korea
[6] Konkuk Univ, KU Open Innovat Ctr, Inst Biomed Sci & Technol, 120 Neungdong Ro, Seoul 05029, South Korea
[7] Konkuk Univ, Sch Med, Dept Adv Translat Med, 120 Neungdong Ro, Seoul 05029, South Korea
来源
CELL REPORTS | 2019年 / 27卷 / 01期
基金
新加坡国家研究基金会; 欧洲研究理事会;
关键词
NEURAL STEM-CELLS; MOUSE FIBROBLASTS; TRANSCRIPTION FACTORS; GENERATION; PLURIPOTENCY; EXPRESSION; BINDING; STATE; OCT4; SOX2;
D O I
10.1016/j.celrep.2019.03.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Simultaneous expression of Oct4, Klf4, Sox2, and cMyc induces pluripotency in somatic cells (iPSCs). Replacing Oct4 with the neuro-specific factor Brn4 leads to transdifferentiation of fibroblasts into induced neural stem cells (iNSCs). However, Brn4 was recently found to induce transient acquisition of pluripotency before establishing the neural fate. We employed genetic lineage tracing and found that induction of iNSCs with individual vectors leads to direct lineage conversion. In contrast, polycistronic expression produces a Brn4-Klf4 fusion protein that enables induction of pluripotency. Our study demonstrates that a combination of pluripotency and tissue-specific factors allows direct somatic cell transdifferentiation, bypassing the acquisition of a pluripotent state. This result has major implications for lineage conversion technologies, which hold potential for providing a safer alternative to iPSCs for clinical application both in vitro and in vivo.
引用
收藏
页码:30 / +
页数:14
相关论文
共 50 条
  • [1] Somatic Lineage Reprogramming
    Shelby, Hannah
    Shelby, Tara
    Wernig, Marius
    COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2022, 14 (10):
  • [2] Direct somatic lineage conversion
    Tanabe, Koji
    Haag, Daniel
    Wernig, Marius
    PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2015, 370 (1680)
  • [3] Lineage conversion methodologies meet the reprogramming toolbox
    Sancho-Martinez, Ignacio
    Baek, Sung Hee
    Izpisua Belmonte, Juan Carlos
    NATURE CELL BIOLOGY, 2012, 14 (09) : 892 - 899
  • [4] Lineage conversion methodologies meet the reprogramming toolbox
    Ignacio Sancho-Martinez
    Sung Hee Baek
    Juan Carlos Izpisua Belmonte
    Nature Cell Biology, 2012, 14 : 892 - 899
  • [5] Reprogramming somatic gene activity by fusion with pluripotent cells
    Jeong Tae Do
    Dong Wook Han
    Hans R. Schöler
    Stem Cell Reviews, 2006, 2 : 257 - 264
  • [6] Reprogramming somatic gene activity by fusion with pluripotent cells
    Do, Jeong Tae
    Han, Dong Wook
    Schoeler, Hans R.
    STEM CELL REVIEWS, 2006, 2 (04): : 257 - 264
  • [7] Reprogramming somatic cells towards pluripotency by cellular fusion
    Soza-Ried, Jorge
    Fisher, Amanda G.
    CURRENT OPINION IN GENETICS & DEVELOPMENT, 2012, 22 (05) : 459 - 465
  • [8] Bioinformatic and Genomic Analyses of Cellular Reprogramming and Direct Lineage Conversion
    Kareta M.S.
    Current Pharmacology Reports, 2016, 2 (3) : 103 - 112
  • [9] Reprogramming lineage identity through cell-cell fusion
    Brown, Karen E.
    Fisher, Amanda G.
    CURRENT OPINION IN GENETICS & DEVELOPMENT, 2021, 70 : 15 - 23
  • [10] Potential Strategies for Cardiac Diseases: Lineage Reprogramming of Somatic Cells into Induced Cardiomyocytes
    Wang, Mingyu
    Ling, Wenhui
    Xiong, Chunxia
    Xie, Dengfeng
    Chu, Xinyue
    Li, Yunxin
    Qiu, Xiaoyan
    Li, Yuemin
    Xiao, Xiong
    CELLULAR REPROGRAMMING, 2019, 21 (02) : 63 - 77