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Direct Conversion of Human Urine Cells to Neurons by Small Molecules
Transdifferentiation of other cell type into human neuronal cells (hNCs) provides a platform for neural disease modeling, drug screening and potential cell-based therapies. Among all of the cell donor sources, human urine cells (hUCs) are convenient to obtain without invasive harvest procedure. Here...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854089/ https://www.ncbi.nlm.nih.gov/pubmed/31723223 http://dx.doi.org/10.1038/s41598-019-53007-6 |
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author | Xu, Guosheng Wu, Feima Gu, Xiaotong Zhang, Jiaye You, Kai Chen, Yan Getachew, Anteneh Zhuang, Yuanqi Zhong, Xiaofen Lin, Zuoxian Guo, Dongsheng Yang, Fan Pan, Tingcai Wei, Hongcheng Li, Yin-xiong |
author_facet | Xu, Guosheng Wu, Feima Gu, Xiaotong Zhang, Jiaye You, Kai Chen, Yan Getachew, Anteneh Zhuang, Yuanqi Zhong, Xiaofen Lin, Zuoxian Guo, Dongsheng Yang, Fan Pan, Tingcai Wei, Hongcheng Li, Yin-xiong |
author_sort | Xu, Guosheng |
collection | PubMed |
description | Transdifferentiation of other cell type into human neuronal cells (hNCs) provides a platform for neural disease modeling, drug screening and potential cell-based therapies. Among all of the cell donor sources, human urine cells (hUCs) are convenient to obtain without invasive harvest procedure. Here, we report a novel approach for the transdifferentiation of hUCs into hNCs. Our study demonstrated that a combination of seven small molecules (CAYTFVB) cocktail induced transdifferentiation of hUCs into hNCs. These chemical-induced neuronal cells (CiNCs) exhibited typical neuron-like morphology and expressed mature neuronal markers. The neuronal-like morphology revealed in day 1, and the Tuj1-positive CiNCs reached to about 58% in day 5 and 38.36% Tuj1+/MAP2+ double positive cells in day 12. Partial electrophysiological properties of CiNCs was obtained using patch clamp. Most of the CiNCs generated using our protocol were glutamatergic neuron populations, whereas motor neurons, GABAergic or dopaminergic neurons were merely detected. hUCs derived from different donors were converted into CiNCs in this work. This method may provide a feasible and noninvasive approach for reprogramming hNCs from hUCs for disease models and drug screening. |
format | Online Article Text |
id | pubmed-6854089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68540892019-11-19 Direct Conversion of Human Urine Cells to Neurons by Small Molecules Xu, Guosheng Wu, Feima Gu, Xiaotong Zhang, Jiaye You, Kai Chen, Yan Getachew, Anteneh Zhuang, Yuanqi Zhong, Xiaofen Lin, Zuoxian Guo, Dongsheng Yang, Fan Pan, Tingcai Wei, Hongcheng Li, Yin-xiong Sci Rep Article Transdifferentiation of other cell type into human neuronal cells (hNCs) provides a platform for neural disease modeling, drug screening and potential cell-based therapies. Among all of the cell donor sources, human urine cells (hUCs) are convenient to obtain without invasive harvest procedure. Here, we report a novel approach for the transdifferentiation of hUCs into hNCs. Our study demonstrated that a combination of seven small molecules (CAYTFVB) cocktail induced transdifferentiation of hUCs into hNCs. These chemical-induced neuronal cells (CiNCs) exhibited typical neuron-like morphology and expressed mature neuronal markers. The neuronal-like morphology revealed in day 1, and the Tuj1-positive CiNCs reached to about 58% in day 5 and 38.36% Tuj1+/MAP2+ double positive cells in day 12. Partial electrophysiological properties of CiNCs was obtained using patch clamp. Most of the CiNCs generated using our protocol were glutamatergic neuron populations, whereas motor neurons, GABAergic or dopaminergic neurons were merely detected. hUCs derived from different donors were converted into CiNCs in this work. This method may provide a feasible and noninvasive approach for reprogramming hNCs from hUCs for disease models and drug screening. Nature Publishing Group UK 2019-11-13 /pmc/articles/PMC6854089/ /pubmed/31723223 http://dx.doi.org/10.1038/s41598-019-53007-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Xu, Guosheng Wu, Feima Gu, Xiaotong Zhang, Jiaye You, Kai Chen, Yan Getachew, Anteneh Zhuang, Yuanqi Zhong, Xiaofen Lin, Zuoxian Guo, Dongsheng Yang, Fan Pan, Tingcai Wei, Hongcheng Li, Yin-xiong Direct Conversion of Human Urine Cells to Neurons by Small Molecules |
title | Direct Conversion of Human Urine Cells to Neurons by Small Molecules |
title_full | Direct Conversion of Human Urine Cells to Neurons by Small Molecules |
title_fullStr | Direct Conversion of Human Urine Cells to Neurons by Small Molecules |
title_full_unstemmed | Direct Conversion of Human Urine Cells to Neurons by Small Molecules |
title_short | Direct Conversion of Human Urine Cells to Neurons by Small Molecules |
title_sort | direct conversion of human urine cells to neurons by small molecules |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854089/ https://www.ncbi.nlm.nih.gov/pubmed/31723223 http://dx.doi.org/10.1038/s41598-019-53007-6 |
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