Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation

A human induced pluripotent stem cell (iPSC) line was generated from patient with type 1 neurofibromatosis (NF-1), carrying heterozygous mutation in NF1 gene. Peripheral blood mononuclear cells (PBMCs) were reprogrammed using non-integrating delivery of KFL4, OCT4, SOX2, BCL-XL and c-MYC. The iPSC l...

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Main Authors: Hongmei Xin, Yixiao Li, Kaihui Zhang, Aihua Ji, Meili Fan
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506124002666
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author Hongmei Xin
Yixiao Li
Kaihui Zhang
Aihua Ji
Meili Fan
author_facet Hongmei Xin
Yixiao Li
Kaihui Zhang
Aihua Ji
Meili Fan
author_sort Hongmei Xin
collection DOAJ
description A human induced pluripotent stem cell (iPSC) line was generated from patient with type 1 neurofibromatosis (NF-1), carrying heterozygous mutation in NF1 gene. Peripheral blood mononuclear cells (PBMCs) were reprogrammed using non-integrating delivery of KFL4, OCT4, SOX2, BCL-XL and c-MYC. The iPSC line expresses pluripotency markers, displays a normal karyotype, and is able to differentiate into three germ layers in vitro. This iPSC line represents a valuable cell model for NF1 in humans.
format Article
id doaj-art-013e47ee313d4fd2b40ec1c3e3ea1a3c
institution Kabale University
issn 1873-5061
language English
publishDate 2024-12-01
publisher Elsevier
record_format Article
series Stem Cell Research
spelling doaj-art-013e47ee313d4fd2b40ec1c3e3ea1a3c2024-12-13T10:56:50ZengElsevierStem Cell Research1873-50612024-12-0181103568Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutationHongmei Xin0Yixiao Li1Kaihui Zhang2Aihua Ji3Meili Fan4Pediatric Research Institute, Children’s Hospital Affiliated to Shandong University, Jinan 250022, ChinaPediatric Research Institute, Children’s Hospital Affiliated to Shandong University, Jinan 250022, China; Department of Ophthalmology, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan 250001, ChinaPediatric Research Institute, Children’s Hospital Affiliated to Shandong University, Jinan 250022, ChinaDepartment of Dermatology, Children’s Hospital Affiliated to Shandong University (Jinan Children’s Hospital), Jinan, Shandong 250022, China; Corresponding authors.Tuina Department, Children’s Hospital Affiliated to Shandong University (Jinan Children’s Hospital), Jinan, Shandong 250022, China; Corresponding authors.A human induced pluripotent stem cell (iPSC) line was generated from patient with type 1 neurofibromatosis (NF-1), carrying heterozygous mutation in NF1 gene. Peripheral blood mononuclear cells (PBMCs) were reprogrammed using non-integrating delivery of KFL4, OCT4, SOX2, BCL-XL and c-MYC. The iPSC line expresses pluripotency markers, displays a normal karyotype, and is able to differentiate into three germ layers in vitro. This iPSC line represents a valuable cell model for NF1 in humans.http://www.sciencedirect.com/science/article/pii/S1873506124002666
spellingShingle Hongmei Xin
Yixiao Li
Kaihui Zhang
Aihua Ji
Meili Fan
Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
Stem Cell Research
title Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
title_full Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
title_fullStr Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
title_full_unstemmed Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
title_short Generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with NF1 mutation
title_sort generation of an induced pluripotent stem cell line from a type 1 neurofibromatosis patient with nf1 mutation
url http://www.sciencedirect.com/science/article/pii/S1873506124002666
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