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Generation of a PPM1A-deficient human induced pluripotent stem cell line using CRISPR-Cas9 technology.
Guo, Xinrui; Zhao, Kui; Zhang, Yanqi; Zhou, Tiancheng; Pan, Guangjin.
Affiliation
  • Guo X; Shandong Medicinal Biotechnology Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250012, China. Electronic address: guo_xinrui@gibh.ac.cn.
  • Zhao K; Department of Hematology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou 510630, China.
  • Zhang Y; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Center for Cell Lineage and Development, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China.
  • Zhou T; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Center for Cell Lineage and Development, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China.
  • Pan G; Shandong Medicinal Biotechnology Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250012, China; Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Center for Cell Lineage and Development, Guangzhou Institutes of Biomedicine and Hea
Stem Cell Res ; 77: 103420, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38643711
ABSTRACT
PPM1A is a member of the serine/threonine protein phosphatase family. It can bind to a variety of proteins to dephosphorylate them, and extensively regulates many life activities such as cell growth, cell stress, immune response, and tumor formation. Here we constructed a human induced pluripotent stem cell (hiPSC) line with knockout of PPM1A using CRISPR/Cas9-mediated gene targeting. This cell line exhibits normal karyotype, pluripotency, and trilineage differentiation potential, which could provide a useful cellular resource for exploring the mechanism of PPM1A in regulating downstream signaling pathways and explore the application of PPM1A in anti-tumor and anti-infection.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Induced Pluripotent Stem Cells / CRISPR-Cas Systems / Protein Phosphatase 2C Limits: Humans Language: En Journal: Stem Cell Res Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Induced Pluripotent Stem Cells / CRISPR-Cas Systems / Protein Phosphatase 2C Limits: Humans Language: En Journal: Stem Cell Res Year: 2024 Document type: Article
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