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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
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