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Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle

BACKGROUND: In the brain of adult mammals, neural stem cells persist in the subventricular zone of the lateral ventricle and the subgranular zone of the dentate gyrus, which are specialized niches with proliferative capacity. Most neural stem cells are in a quiescent state, but in response to extrin...

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Autores principales: Li, Wen, Wang, Shanshan, He, Hui, Qin, Jianbing, Cheng, Xiang, Zhao, Heyan, Tian, Meiling, Zhang, Xinhua, Jin, Guohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796549/
https://www.ncbi.nlm.nih.gov/pubmed/33422130
http://dx.doi.org/10.1186/s13287-020-02119-2
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author Li, Wen
Wang, Shanshan
He, Hui
Qin, Jianbing
Cheng, Xiang
Zhao, Heyan
Tian, Meiling
Zhang, Xinhua
Jin, Guohua
author_facet Li, Wen
Wang, Shanshan
He, Hui
Qin, Jianbing
Cheng, Xiang
Zhao, Heyan
Tian, Meiling
Zhang, Xinhua
Jin, Guohua
author_sort Li, Wen
collection PubMed
description BACKGROUND: In the brain of adult mammals, neural stem cells persist in the subventricular zone of the lateral ventricle and the subgranular zone of the dentate gyrus, which are specialized niches with proliferative capacity. Most neural stem cells are in a quiescent state, but in response to extrinsic stimuli, they can exit from quiescence and become reactivated to produce new neurons, so neural stem cells are considered to be a potential source for cell replacement therapy of many nervous system diseases. We characterized the expression of Ndel1 during the differentiation of neural stem cells induced by hippocampus exosomes, and assessed the effect of Ndel1 on neural stem cells differentiation. METHODS: Hippocampal exosomes were isolated and extracted, and co-cultured exosomes with neural stem cells. Western blot, flow cytometry, and immunofluorescence analyses were used to analyze expression of neuronal markers. Further, utilizing high-throughput RNA sequencing technology, we found that nudE neurodevelopment protein 1-like 1 was significantly upregulated in exosomes derived from denervated hippocampus, and then characterized its mechanism and function during neural stem cells differentiation by qRT-PCR, western blot, flow cytometry, and immunofluorescence analyses. RESULTS: Our results revealed that exosomes of denervated hippocampus promoted the differentiation of neural stem cells into neuron. Hence, we identified that nudE neurodevelopment protein 1-like 1 was significantly upregulated and highly expressed in the nervous system. In addition, we found that miR-107-3p may regulate neural stem cell differentiation by targeting Ndel1. CONCLUSIONS: Our results revealed that deafferentation of the hippocampal exosomes co-cultured with neural stem cells could promote them to differentiate into neurons. Hence, we found that miR-107-3p may regulate neural stem cells differentiation by targeting Ndel1. Importantly, Ndel1 enhanced spatial learning and hippocampal neurogenesis in rats after fimbria fornix transection in vivo. These findings set the stage for a better understanding of neurogenesis, a process that 1 day may inspire new treatments for central nervous system diseases.
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spelling pubmed-77965492021-01-11 Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle Li, Wen Wang, Shanshan He, Hui Qin, Jianbing Cheng, Xiang Zhao, Heyan Tian, Meiling Zhang, Xinhua Jin, Guohua Stem Cell Res Ther Research BACKGROUND: In the brain of adult mammals, neural stem cells persist in the subventricular zone of the lateral ventricle and the subgranular zone of the dentate gyrus, which are specialized niches with proliferative capacity. Most neural stem cells are in a quiescent state, but in response to extrinsic stimuli, they can exit from quiescence and become reactivated to produce new neurons, so neural stem cells are considered to be a potential source for cell replacement therapy of many nervous system diseases. We characterized the expression of Ndel1 during the differentiation of neural stem cells induced by hippocampus exosomes, and assessed the effect of Ndel1 on neural stem cells differentiation. METHODS: Hippocampal exosomes were isolated and extracted, and co-cultured exosomes with neural stem cells. Western blot, flow cytometry, and immunofluorescence analyses were used to analyze expression of neuronal markers. Further, utilizing high-throughput RNA sequencing technology, we found that nudE neurodevelopment protein 1-like 1 was significantly upregulated in exosomes derived from denervated hippocampus, and then characterized its mechanism and function during neural stem cells differentiation by qRT-PCR, western blot, flow cytometry, and immunofluorescence analyses. RESULTS: Our results revealed that exosomes of denervated hippocampus promoted the differentiation of neural stem cells into neuron. Hence, we identified that nudE neurodevelopment protein 1-like 1 was significantly upregulated and highly expressed in the nervous system. In addition, we found that miR-107-3p may regulate neural stem cell differentiation by targeting Ndel1. CONCLUSIONS: Our results revealed that deafferentation of the hippocampal exosomes co-cultured with neural stem cells could promote them to differentiate into neurons. Hence, we found that miR-107-3p may regulate neural stem cells differentiation by targeting Ndel1. Importantly, Ndel1 enhanced spatial learning and hippocampal neurogenesis in rats after fimbria fornix transection in vivo. These findings set the stage for a better understanding of neurogenesis, a process that 1 day may inspire new treatments for central nervous system diseases. BioMed Central 2021-01-09 /pmc/articles/PMC7796549/ /pubmed/33422130 http://dx.doi.org/10.1186/s13287-020-02119-2 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Wen
Wang, Shanshan
He, Hui
Qin, Jianbing
Cheng, Xiang
Zhao, Heyan
Tian, Meiling
Zhang, Xinhua
Jin, Guohua
Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
title Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
title_full Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
title_fullStr Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
title_full_unstemmed Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
title_short Expression and function of Ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
title_sort expression and function of ndel1 during the differentiation of neural stem cells induced by hippocampal exosomesticle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796549/
https://www.ncbi.nlm.nih.gov/pubmed/33422130
http://dx.doi.org/10.1186/s13287-020-02119-2
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