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Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure
Linx is a member of the leucine-rich repeat and immunoglobulin family of membrane proteins which has critical roles in the development of the peripheral nervous system and forebrain connectivity. A previous study showed that Linx is expressed in projection neurons in the cortex and in cells that com...
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/PMC5940738/ https://www.ncbi.nlm.nih.gov/pubmed/29739947 http://dx.doi.org/10.1038/s41598-018-24064-0 |
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author | Abudureyimu, Shaniya Asai, Naoya Enomoto, Atsushi Weng, Liang Kobayashi, Hiroki Wang, Xiaoze Chen, Chen Mii, Shinji Takahashi, Masahide |
author_facet | Abudureyimu, Shaniya Asai, Naoya Enomoto, Atsushi Weng, Liang Kobayashi, Hiroki Wang, Xiaoze Chen, Chen Mii, Shinji Takahashi, Masahide |
author_sort | Abudureyimu, Shaniya |
collection | PubMed |
description | Linx is a member of the leucine-rich repeat and immunoglobulin family of membrane proteins which has critical roles in the development of the peripheral nervous system and forebrain connectivity. A previous study showed that Linx is expressed in projection neurons in the cortex and in cells that comprise the passage to the prethalamus that form the internal capsule, indicating the involvement of Linx in axon guidance and cell-cell communication. In this study, we found that Linx-deficient mice develop severe hydrocephalus and die perinatally by unknown mechanisms. Importantly, mice heterozygous for the linx gene exhibited defects in the development of the anterior commissure in addition to hydrocephalus, indicating haploinsufficiency of the linx gene in forebrain development. In N1E-115 neuroblastoma cells and primary cultured hippocampal neurons, Linx depletion led to impaired neurite extension and an increase in cell body size. Consistent with this, but of unknown significance, we found that Linx interacts with and upregulates the activity of Rho-kinase, a modulator of many cellular processes including cytoskeletal organization. These data suggest a role for Linx in the regulation of complex forebrain connectivity, and future identification of its extracellular ligand(s) will help clarify this function. |
format | Online Article Text |
id | pubmed-5940738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59407382018-05-11 Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure Abudureyimu, Shaniya Asai, Naoya Enomoto, Atsushi Weng, Liang Kobayashi, Hiroki Wang, Xiaoze Chen, Chen Mii, Shinji Takahashi, Masahide Sci Rep Article Linx is a member of the leucine-rich repeat and immunoglobulin family of membrane proteins which has critical roles in the development of the peripheral nervous system and forebrain connectivity. A previous study showed that Linx is expressed in projection neurons in the cortex and in cells that comprise the passage to the prethalamus that form the internal capsule, indicating the involvement of Linx in axon guidance and cell-cell communication. In this study, we found that Linx-deficient mice develop severe hydrocephalus and die perinatally by unknown mechanisms. Importantly, mice heterozygous for the linx gene exhibited defects in the development of the anterior commissure in addition to hydrocephalus, indicating haploinsufficiency of the linx gene in forebrain development. In N1E-115 neuroblastoma cells and primary cultured hippocampal neurons, Linx depletion led to impaired neurite extension and an increase in cell body size. Consistent with this, but of unknown significance, we found that Linx interacts with and upregulates the activity of Rho-kinase, a modulator of many cellular processes including cytoskeletal organization. These data suggest a role for Linx in the regulation of complex forebrain connectivity, and future identification of its extracellular ligand(s) will help clarify this function. Nature Publishing Group UK 2018-05-08 /pmc/articles/PMC5940738/ /pubmed/29739947 http://dx.doi.org/10.1038/s41598-018-24064-0 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 Abudureyimu, Shaniya Asai, Naoya Enomoto, Atsushi Weng, Liang Kobayashi, Hiroki Wang, Xiaoze Chen, Chen Mii, Shinji Takahashi, Masahide Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure |
title | Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure |
title_full | Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure |
title_fullStr | Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure |
title_full_unstemmed | Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure |
title_short | Essential Role of Linx/Islr2 in the Development of the Forebrain Anterior Commissure |
title_sort | essential role of linx/islr2 in the development of the forebrain anterior commissure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940738/ https://www.ncbi.nlm.nih.gov/pubmed/29739947 http://dx.doi.org/10.1038/s41598-018-24064-0 |
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