Generation of multiple human iPSC lines from peripheral blood mononuclear cells of two SLC2A3 deletion and two SLC2A3 duplication carriers

G.C. Ziegler*, F. Radtke, M.R. Vitale, A. Preusse, E. Klopocki, S. Herms, K.P. Lesch

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Copy number variants of SLC2A3, which encodes the glucose transporter GLUT3, are associated with several neuropsychiatric and cardiac diseases. Here, we report the successful reprogramming of peripheral blood mononuclear cells from two SLC2A3 duplication and two SLC2A3 deletion carriers and subsequent generation of two transgene-free iPSC clones per donor by Sendai viral transduction. All eight clones represent bona fide hiPSCs with high expression of pluripotency genes, ability to differentiate into cells of all three germ layers and normal karyotype. The generated cell lines will be helpful to enlighten the role of glucometabolic alterations in pathophysiological processes shared across organ boundaries.
Original languageEnglish
Article number102526
Number of pages5
JournalStem Cell Research
Volume56
DOIs
Publication statusPublished - 1 Oct 2021

Keywords

  • CONGENITAL HEART-DEFECTS
  • TRANSPORTER GENE SLC2A3
  • COPY-NUMBER VARIATION

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