Generation and characterization of induced pluripotent stem cell (iPSC) lines from patients affected with Tay-Sachs and Sandhoff disease

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Authors: Vukasin M. Jovanovic, Catherine Z. Chen, Camilo Toro, Kerstin A. Hurd, Jizhong Zou, Cynthia J. Tifft, Wei Zheng, Mark J. Henderson, Juan Marugán, Carlos A. Tristan
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References: 4

Abstract

Tay-Sachs and Sandhoff diseases, are sphingolipidoses caused by rare genetic mutations in the HEXA and HEXB genes, that encode the alpha and beta subunits of lysosomal hexosaminidase, respectively. Here, we report the generation and characterization of three Tay-Sachs and one Sandhoff iPSC lines derived from patients with late-onset disease carrying mutations at the HEXA or HEXB gene. The Tay-Sachs patients carried either homozygous or complex heterozygous mutations in the HEXA gene. The Sandhoff patient carried a heterozygous mutation in the HEXB gene. These four iPSC lines will serve as a valuable resource for the development of in vitro lysosomal storage disease models and therapeutic drug development.

Fields of Study & Subjects

Lysosomal Storage Disorders Research Pluripotent Stem Cells Research Glycogen Storage Diseases and Myoclonus

Publication details

Journal / source
Stem Cell Research
Volume
92
Pages
103949–103949
Publication date
3 March 2026
Language
EN