Simultaneous reprogramming and gene correction to generate six iPSC lines and isogenic controls from individuals with neurofibromatosis type 1

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Authors: Kiymet Bozaoglu, Sarah Jessica Massie, Friederike Elise Irion, Kayli C. Davies, Inbal Kantor, Mai Raabus, Kristina M. Haebich, Katerina Vlahos, Sara E. Howden, Jordan M. Wright, Jonathan M. Payne, Paul J. Lockhart
Cited by: 0
References: 9

Abstract

Neurofibromatosis type 1 (NF1) is a neurodevelopmental disorder that affects ∼ 1: 2700 individuals (Lee et al., 2023) however the underlying pathogenic mechanisms are poorly understood. In this study, we performed simultaneous reprogramming and CRISPR-Cas9 genome editing to generate pluripotent stem cell (iPSCs) lines and their respective isogenic controls from six individuals with different pathogenic NF1 variants. All iPSC lines had a normal karyotype, were pluripotent and able to differentiate into the three embryonic germ layers. These iPSC lines are valuable pre-clinical models to investigate the pathomechanisms of NF1 and can be used for future screening to identify new therapeutic treatments for NF1.

Fields of Study & Subjects

Neurofibromatosis and Schwannoma Cases Tuberous Sclerosis Complex Research Pluripotent Stem Cells Research

Publication details

Journal / source
Stem Cell Research
Volume
90
Pages
103904–103904
Publication date
1 January 2026
Language
EN