HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Establishment and directed differentiation of induced pluripotent stem cells from glycogen storage disease type Ib patient.

Abstract
Glycogen storage disease type Ib (GSDIb) is caused by a deficiency in the glucose-6-phosphate transporter (G6PT), which leads to neutrophil dysfunction. However, the underlying causes of these dysfunctions and their relationship with glucose homeostasis are unclear. Induced pluripotent stem cells (iPSCs) hold a great promise for advances in developmental biology, cell-based therapy and modeling of human disease. Here, we examined the use of iPSCs as a model for GSDIb. In this study, one 2-year-old patient was genetically screened and diagnosed with GSDIb. We established iPSCs and differentiated these cells into hepatocytes and neutrophils, which comprise the main pathological components of GSDIb. Cells that differentiated into hepatocytes exhibited characteristic albumin secretion and indocyanine green uptake. Moreover, iPSC-derived cells generated from patients with GSDIb metabolic abnormalities recapitulated key pathological features of the diseases affecting the patients from whom they were derived, such as glycogen, lactate, pyruvate and lipid accumulation. Cells that were differentiated into neutrophils also showed the GSDIb pathology. In addition to the expression of neutrophil markers, we showed increased superoxide anion production, increased annexin V binding and activation of caspase-3 and caspase-9, consistent with the GSDIb patient's neutrophils. These results indicate valuable tools for the analysis of this pathology and the development of future treatments.
AuthorsDaisuke Satoh, Tohru Maeda, Tetsuya Ito, Yoko Nakajima, Mariko Ohte, Akane Ukai, Katsunori Nakamura, Shin Enosawa, Masashi Toyota, Yoshitaka Miyagawa, Hajime Okita, Nobutaka Kiyokawa, Hidenori Akutsu, Akihiro Umezawa, Tamihide Matsunaga
JournalGenes to cells : devoted to molecular & cellular mechanisms (Genes Cells) Vol. 18 Issue 12 Pg. 1053-69 (Dec 2013) ISSN: 1365-2443 [Electronic] England
PMID24581426 (Publication Type: Journal Article)
Copyright© 2013 The Authors Genes to Cells © 2013 by the Molecular Biology Society of Japan and Wiley Publishing Asia Pty Ltd.
Topics
  • Cell Differentiation
  • Cells, Cultured
  • Child, Preschool
  • Glycogen Storage Disease Type I (metabolism, pathology)
  • Hepatocytes (metabolism, pathology)
  • Humans
  • Induced Pluripotent Stem Cells (metabolism, pathology)
  • Neutrophils (metabolism, pathology)
  • Oxidative Stress

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: