Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells

Induced pluripotent stem cells (iPSCs) have provided new opportunities for motor neuron disease (MND) modeling, drug screening, and cellular therapeutic development. Among the various types of iPSCs, urine-derived iPSCs have become a promising source of stem cells because they can be safely and noni...

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Main Authors: Huan Yi, Bingbing Xie, Ben Liu, Xuan Wang, Li Xu, Jia Liu, Min Li, Xiufeng Zhong, Fuhua Peng
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2018/3628578
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author Huan Yi
Bingbing Xie
Ben Liu
Xuan Wang
Li Xu
Jia Liu
Min Li
Xiufeng Zhong
Fuhua Peng
author_facet Huan Yi
Bingbing Xie
Ben Liu
Xuan Wang
Li Xu
Jia Liu
Min Li
Xiufeng Zhong
Fuhua Peng
author_sort Huan Yi
collection DOAJ
description Induced pluripotent stem cells (iPSCs) have provided new opportunities for motor neuron disease (MND) modeling, drug screening, and cellular therapeutic development. Among the various types of iPSCs, urine-derived iPSCs have become a promising source of stem cells because they can be safely and noninvasively isolated and easily reprogrammed. Here, for the first time, we differentiated urine-derived iPSCs (urine-iPSCs) into motor neurons (MNs) and compared the capacity of urine-iPSCs and cord-blood-derived iPSCs (B-iPSCs) to differentiate into MNs. With the use of small molecules, mature MNs were generated from urine-iPSCs as early as 26 days in culture. Furthermore, in coculture with muscle cells, MNs projected long axons and formed neuromuscular junctions (NMJs). Immunofluorescence and PCR confirmed the expression levels of both MN and NMJ markers. The comparison of the ratios of positive labeling for MN markers between urine-iPSCs and B-iPSCs demonstrated that the differentiation potentials of these cells were not significantly different. The abovementioned results indicate that urine-iPSCs are a new, promising source of stem cells for MND modeling and further cellular therapeutic development.
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institution Kabale University
issn 1687-966X
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publishDate 2018-01-01
publisher Wiley
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series Stem Cells International
spelling doaj-art-45582d0fe179435398199378a090aafe2025-02-03T01:20:33ZengWileyStem Cells International1687-966X1687-96782018-01-01201810.1155/2018/36285783628578Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem CellsHuan Yi0Bingbing Xie1Ben Liu2Xuan Wang3Li Xu4Jia Liu5Min Li6Xiufeng Zhong7Fuhua Peng8Department of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong 510600, ChinaDepartment of Dermatology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong 510600, ChinaDepartment of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong 510630, ChinaInduced pluripotent stem cells (iPSCs) have provided new opportunities for motor neuron disease (MND) modeling, drug screening, and cellular therapeutic development. Among the various types of iPSCs, urine-derived iPSCs have become a promising source of stem cells because they can be safely and noninvasively isolated and easily reprogrammed. Here, for the first time, we differentiated urine-derived iPSCs (urine-iPSCs) into motor neurons (MNs) and compared the capacity of urine-iPSCs and cord-blood-derived iPSCs (B-iPSCs) to differentiate into MNs. With the use of small molecules, mature MNs were generated from urine-iPSCs as early as 26 days in culture. Furthermore, in coculture with muscle cells, MNs projected long axons and formed neuromuscular junctions (NMJs). Immunofluorescence and PCR confirmed the expression levels of both MN and NMJ markers. The comparison of the ratios of positive labeling for MN markers between urine-iPSCs and B-iPSCs demonstrated that the differentiation potentials of these cells were not significantly different. The abovementioned results indicate that urine-iPSCs are a new, promising source of stem cells for MND modeling and further cellular therapeutic development.http://dx.doi.org/10.1155/2018/3628578
spellingShingle Huan Yi
Bingbing Xie
Ben Liu
Xuan Wang
Li Xu
Jia Liu
Min Li
Xiufeng Zhong
Fuhua Peng
Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells
Stem Cells International
title Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells
title_full Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells
title_fullStr Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells
title_full_unstemmed Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells
title_short Derivation and Identification of Motor Neurons from Human Urine-Derived Induced Pluripotent Stem Cells
title_sort derivation and identification of motor neurons from human urine derived induced pluripotent stem cells
url http://dx.doi.org/10.1155/2018/3628578
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