Establishment of a non-integrated iPSC (SDQLCHi068-A) line derived from a patient with autosomal dominant immunodeficiency-14A carrying a heterozygous mutation (c.3061G>A) in PIK3CD gene

Stem Cell Res. 2024 Jun:77:103385. doi: 10.1016/j.scr.2024.103385. Epub 2024 Mar 11.

Abstract

Phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta (PIK3CD) gene (OMIM#602839) encodes the p110δ catalytic subunit, mainly expressed in immune cells, and is associated with autosomal dominant immunodeficiency-14A with lymphoproliferation (IMD14A, #615513). We generated a human iPS cell line from a 50-month-old boy with IMD14A carrying a heterozygous mutation (c.3061G>A, p.E1021K) in PIK3CD gene. This cell line retains the original mutation site and shows differentiation potential towards three germ layers in vitro, which can be used as a disease model for research.

MeSH terms

  • Cell Differentiation
  • Cell Line
  • Child, Preschool
  • Class I Phosphatidylinositol 3-Kinases* / genetics
  • Class I Phosphatidylinositol 3-Kinases* / metabolism
  • Heterozygote*
  • Humans
  • Immunologic Deficiency Syndromes / genetics
  • Induced Pluripotent Stem Cells* / metabolism
  • Male
  • Mutation

Substances

  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CD protein, human