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Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway
The neural stem cells (NSCs) of the subventricular zone (SVZ) reside within a specialized niche critical for neurogenesis. Hemopexin, a plasma glycoprotein, has been extensively studied as a heme scavenger at the systemic level. However, little is known about its function in the central nervous syst...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833796/ https://www.ncbi.nlm.nih.gov/pubmed/29449593 http://dx.doi.org/10.1038/s41419-018-0328-0 |
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author | Zhu, Yanling Qiu, Yang Chen, Mengjia Zhang, Yi Cao, Li Su, Zhida Yuan, Yimin Huang, Aijun Pu, Yinyan He, Cheng |
author_facet | Zhu, Yanling Qiu, Yang Chen, Mengjia Zhang, Yi Cao, Li Su, Zhida Yuan, Yimin Huang, Aijun Pu, Yinyan He, Cheng |
author_sort | Zhu, Yanling |
collection | PubMed |
description | The neural stem cells (NSCs) of the subventricular zone (SVZ) reside within a specialized niche critical for neurogenesis. Hemopexin, a plasma glycoprotein, has been extensively studied as a heme scavenger at the systemic level. However, little is known about its function in the central nervous system, especially in neurogenesis. In the present study, we demonstrate that deletion of hemopexin leads to neurogenic abnormalities in the SVZ/olfactory bulb (OB) pathway. The lateral ventricle is enlarged in hemopexin-deficient mice, and more apoptosis was observed in Dcx+ cells. Lineage differentiation of NSCs was also inhibited in the SVZ of hemopexin-deficient mice, with more stem cells stayed in an undifferentiated, GFAP+ radial glia-like cell stage. Moreover, hemopexin deletion resulted in impaired neuroblast migration in the rostral migratory stream. Furthermore, exogenous hemopexin protein inhibited apoptosis and promoted the migration and differentiation of cultured NSCs. Finally, immunohistochemical analysis demonstrated that deletion of hemopexin reduced the number of interneurons in the OB. Together, these results suggest a new molecular mechanism for the NSC niche that regulates adult neurogenesis in the SVZ/OB pathway. Our findings may benefit the understanding for olfactory system development. |
format | Online Article Text |
id | pubmed-5833796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58337962018-03-06 Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway Zhu, Yanling Qiu, Yang Chen, Mengjia Zhang, Yi Cao, Li Su, Zhida Yuan, Yimin Huang, Aijun Pu, Yinyan He, Cheng Cell Death Dis Article The neural stem cells (NSCs) of the subventricular zone (SVZ) reside within a specialized niche critical for neurogenesis. Hemopexin, a plasma glycoprotein, has been extensively studied as a heme scavenger at the systemic level. However, little is known about its function in the central nervous system, especially in neurogenesis. In the present study, we demonstrate that deletion of hemopexin leads to neurogenic abnormalities in the SVZ/olfactory bulb (OB) pathway. The lateral ventricle is enlarged in hemopexin-deficient mice, and more apoptosis was observed in Dcx+ cells. Lineage differentiation of NSCs was also inhibited in the SVZ of hemopexin-deficient mice, with more stem cells stayed in an undifferentiated, GFAP+ radial glia-like cell stage. Moreover, hemopexin deletion resulted in impaired neuroblast migration in the rostral migratory stream. Furthermore, exogenous hemopexin protein inhibited apoptosis and promoted the migration and differentiation of cultured NSCs. Finally, immunohistochemical analysis demonstrated that deletion of hemopexin reduced the number of interneurons in the OB. Together, these results suggest a new molecular mechanism for the NSC niche that regulates adult neurogenesis in the SVZ/OB pathway. Our findings may benefit the understanding for olfactory system development. Nature Publishing Group UK 2018-02-15 /pmc/articles/PMC5833796/ /pubmed/29449593 http://dx.doi.org/10.1038/s41419-018-0328-0 Text en © The Author(s) 2018 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 Zhu, Yanling Qiu, Yang Chen, Mengjia Zhang, Yi Cao, Li Su, Zhida Yuan, Yimin Huang, Aijun Pu, Yinyan He, Cheng Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
title | Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
title_full | Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
title_fullStr | Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
title_full_unstemmed | Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
title_short | Hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
title_sort | hemopexin is required for adult neurogenesis in the subventricular zone/olfactory bulb pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833796/ https://www.ncbi.nlm.nih.gov/pubmed/29449593 http://dx.doi.org/10.1038/s41419-018-0328-0 |
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