Cargando…
Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish
Microglia are brain resident macrophages important for brain development, connectivity, homeostasis and disease. However, it is still largely unclear how microglia functions and their identity are regulated at the molecular level. Although recent transcriptomic studies have identified genes specific...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215681/ https://www.ncbi.nlm.nih.gov/pubmed/27757989 http://dx.doi.org/10.1002/glia.23083 |
_version_ | 1782491801394872320 |
---|---|
author | Oosterhof, Nynke Holtman, Inge R. Kuil, Laura E. van der Linde, Herma C. Boddeke, Erik W.G.M. Eggen, Bart J.L. van Ham, Tjakko J. |
author_facet | Oosterhof, Nynke Holtman, Inge R. Kuil, Laura E. van der Linde, Herma C. Boddeke, Erik W.G.M. Eggen, Bart J.L. van Ham, Tjakko J. |
author_sort | Oosterhof, Nynke |
collection | PubMed |
description | Microglia are brain resident macrophages important for brain development, connectivity, homeostasis and disease. However, it is still largely unclear how microglia functions and their identity are regulated at the molecular level. Although recent transcriptomic studies have identified genes specifically expressed in microglia, the function of most of these genes in microglia is still unknown. Here, we performed RNA sequencing on microglia acutely isolated from healthy and neurodegenerative zebrafish brains. We found that a large fraction of the mouse microglial signature is conserved in the zebrafish, corroborating the use of zebrafish to help understand microglial genetics in mammals in addition to studying basic microglia biology. Second, our transcriptome analysis of microglia following neuronal ablation suggested primarily a proliferative response of microglia, which we confirmed by immunohistochemistry and in vivo imaging. Together with the recent improvements in genome editing technology in zebrafish, these data offer opportunities to facilitate functional genetic research on microglia in vivo in the healthy as well as in the diseased brain. GLIA 2016;65:138–149 |
format | Online Article Text |
id | pubmed-5215681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52156812017-01-18 Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish Oosterhof, Nynke Holtman, Inge R. Kuil, Laura E. van der Linde, Herma C. Boddeke, Erik W.G.M. Eggen, Bart J.L. van Ham, Tjakko J. Glia Research Articles Microglia are brain resident macrophages important for brain development, connectivity, homeostasis and disease. However, it is still largely unclear how microglia functions and their identity are regulated at the molecular level. Although recent transcriptomic studies have identified genes specifically expressed in microglia, the function of most of these genes in microglia is still unknown. Here, we performed RNA sequencing on microglia acutely isolated from healthy and neurodegenerative zebrafish brains. We found that a large fraction of the mouse microglial signature is conserved in the zebrafish, corroborating the use of zebrafish to help understand microglial genetics in mammals in addition to studying basic microglia biology. Second, our transcriptome analysis of microglia following neuronal ablation suggested primarily a proliferative response of microglia, which we confirmed by immunohistochemistry and in vivo imaging. Together with the recent improvements in genome editing technology in zebrafish, these data offer opportunities to facilitate functional genetic research on microglia in vivo in the healthy as well as in the diseased brain. GLIA 2016;65:138–149 John Wiley and Sons Inc. 2016-10-19 2017-01 /pmc/articles/PMC5215681/ /pubmed/27757989 http://dx.doi.org/10.1002/glia.23083 Text en © 2016 The Authors. Glia Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Oosterhof, Nynke Holtman, Inge R. Kuil, Laura E. van der Linde, Herma C. Boddeke, Erik W.G.M. Eggen, Bart J.L. van Ham, Tjakko J. Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
title | Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
title_full | Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
title_fullStr | Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
title_full_unstemmed | Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
title_short | Identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
title_sort | identification of a conserved and acute neurodegeneration‐specific microglial transcriptome in the zebrafish |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5215681/ https://www.ncbi.nlm.nih.gov/pubmed/27757989 http://dx.doi.org/10.1002/glia.23083 |
work_keys_str_mv | AT oosterhofnynke identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish AT holtmaninger identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish AT kuillaurae identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish AT vanderlindehermac identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish AT boddekeerikwgm identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish AT eggenbartjl identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish AT vanhamtjakkoj identificationofaconservedandacuteneurodegenerationspecificmicroglialtranscriptomeinthezebrafish |