A human ESC line for efficient CRISPR editing of pluripotent stem cells

被引:2
|
作者
Sintov, Elad [1 ]
Gerace, Dario [1 ]
Melton, Douglas A. [1 ,2 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
关键词
D O I
10.1016/j.scr.2021.102591
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human pluripotent stem cells (hPSC) can be directed to differentiate in vitro into insulin-prorducing beta cells (SC-beta). Although these cells accurately respond to glucose and can reverse diabetes in preclinical models improvments in the final cell products are desirable. For example, safety, controlling the cellular compositions and protection against immune rejection may be addressed by genetic modifications of SC-beta pre-transplantation. To screen for gene targets, we have generated a human embryonic stem cell line (hESC) that constitutively express the enhanced specificity Streptococcus pyogenes Cas9 (eSpCas9) gene, knocked-in into the GAPDH locus.
引用
收藏
页数:4
相关论文
共 50 条
  • [31] Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing
    Bonnycastle, Lori L.
    Swift, Amy J.
    Mansell, Erin C.
    Lee, Angela
    Winnicki, Elizabeth
    Li, Elizabeth S.
    Robertson, Catherine C.
    Parsons, Victoria A.
    Huynh, Trung
    Krilow, Chad
    Mohlke, Karen L.
    Erdos, Michael R.
    Narisu, Narisu
    Collins, Francis S.
    CRISPR JOURNAL, 2024, 7 (01): : 53 - 67
  • [32] Genome Editing in Induced Pluripotent Stem Cells using CRISPR/Cas9
    Ronen Ben Jehuda
    Yuval Shemer
    Ofer Binah
    Stem Cell Reviews and Reports, 2018, 14 : 323 - 336
  • [33] Generation of a MIR5004 knockout cell line from human induced pluripotent stem cells by CRISPR/Cas9 gene editing
    Gulimiheranmu, Maisumu
    Li, Shuang
    Zhou, Junmei
    STEM CELL RESEARCH, 2022, 62
  • [34] Highly efficient genome editing via CRISPR-Cas9 in human pluripotent stem cells is achieved by transient BCL-XL overexpression
    Li, Xiao-Lan
    Li, Guo-Hua
    Fu, Juan
    Fu, Ya-Wen
    Zhang, Lu
    Chen, Wanqiu
    Arakaki, Cameron
    Zhang, Jian-Ping
    Wen, Wei
    Zhao, Mei
    Chen, Weisheng V.
    Botimer, Gary D.
    Baylink, David
    Aranda, Leslie
    Choi, Hannah
    Bechar, Rachel
    Talbot, Prue
    Sun, Chang-Kai
    Cheng, Tao
    Zhang, Xiao-Bing
    NUCLEIC ACIDS RESEARCH, 2018, 46 (19) : 10195 - 10215
  • [35] Generation of a homozygous ZBTB7A knockout human induced pluripotent stem line by CRISPR/Cas9 editing
    Chen, Diyu
    Song, Bing
    Cheng, Yi
    Zhu, Lifen
    Lu, Dian
    Liu, Nengqing
    Yang, Yinghong
    Sun, Xiaofang
    STEM CELL RESEARCH, 2021, 55
  • [36] Focused-ultrasound-mediated CRISPR-Cas9 gene editing in human induced pluripotent stem cells
    Owusu-Yaw, Bernie Simone
    MOLECULAR THERAPY, 2025, 33 (03) : 831 - 832
  • [37] CRISPR-mediated genome editing in human induced pluripotent stem cells for modelling FKRP-deficient dystroglycanopathies
    Kim, J.
    Lana, B.
    Ryan, D.
    Konstantinidis, E.
    Louzada, S.
    Fu, B.
    Yang, F.
    Stemple, D. L.
    Liu, P.
    Muntoni, F.
    Lin, Y-Y.
    NEUROMUSCULAR DISORDERS, 2017, 27 : S12 - S12
  • [38] A Cell-Based Optimised Approach for Rapid and Efficient Gene Editing of Human Pluripotent Stem Cells
    Cuevas-Ocana, Sara
    Yang, Jin Ye
    Aushev, Magomet
    Schlossmacher, George
    Bear, Christine E.
    Hannan, Nicholas R. F.
    Perkins, Neil D.
    Rossant, Janet
    Wong, Amy P.
    Gray, Michael A.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (12)
  • [39] CRISPR-Cas9: a promising tool for gene editing on induced pluripotent stem cells
    Kim, Eun Ji
    Kang, Ki Ho
    Ju, Ji Hyeon
    KOREAN JOURNAL OF INTERNAL MEDICINE, 2017, 32 (01): : 42 - 61
  • [40] Use of CRISPR/Cas ribonucleoproteins for high throughput gene editing of induced pluripotent stem cells
    Wang, Qi
    Chear, Sueanne
    Wing, Kristof
    Stellon, David
    Minh Thuan Nguyen Tran
    Talbot, Jana
    Pebay, Alice
    Hewitt, Alex W.
    Cook, Anthony L.
    METHODS, 2021, 194 : 18 - 29