Cargando…

Distribution of five clinically important neuroglial proteins in the human brain

Glial fibrillary acidic protein (GFAP), myelin basic protein (MBP), neurofilament light chain (NFL), tau and ubiquitin carboxy-terminal hydrolase L1 (UCHL1) are five neuroglial proteins that are used as CSF or blood biomarkers of tissue damage in the nervous system. There is incomplete knowledge of...

Descripción completa

Detalles Bibliográficos
Autores principales: Sjölin, Karl, Kultima, Kim, Larsson, Anders, Freyhult, Eva, Zjukovskaja, Christina, Alkass, Kanar, Burman, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241296/
https://www.ncbi.nlm.nih.gov/pubmed/35765081
http://dx.doi.org/10.1186/s13041-022-00935-6
_version_ 1784737773182255104
author Sjölin, Karl
Kultima, Kim
Larsson, Anders
Freyhult, Eva
Zjukovskaja, Christina
Alkass, Kanar
Burman, Joachim
author_facet Sjölin, Karl
Kultima, Kim
Larsson, Anders
Freyhult, Eva
Zjukovskaja, Christina
Alkass, Kanar
Burman, Joachim
author_sort Sjölin, Karl
collection PubMed
description Glial fibrillary acidic protein (GFAP), myelin basic protein (MBP), neurofilament light chain (NFL), tau and ubiquitin carboxy-terminal hydrolase L1 (UCHL1) are five neuroglial proteins that are used as CSF or blood biomarkers of tissue damage in the nervous system. There is incomplete knowledge of how the concentration of these proteins differs between anatomical regions in the CNS as previous studies have focused on gene expression or non-quantitative protein analyses, limiting the interpretability of these biomarkers. The purpose of this study was to create a map of the tissue content of these proteins in different regions of the CNS. The concentrations of the investigated proteins were determined with ELISA in post mortem tissue homogenates from 17 selected anatomical regions in the CNS from ten deceased donors aged 24 to 50 years. When appropriate, the protein concentrations were adjusted for post-mortem interval. In total, 168 tissue samples were analysed. There was a substantial variation in the concentrations of GFAP, MBP, NFL, tau and UCHL1 between different CNS regions. Highly myelinated areas of the CNS had tenfold higher MBP concentration than cerebral cortex, whereas tau showed an inverse pattern. GFAP, NFL and tau displayed an anteroposterior gradient in cerebral white matter. The cerebellum had low concentrations of all the investigated proteins. In conclusion, the tissue concentrations of GFAP, MBP, NFL, tau and UCHL1 were determined throughout the CNS. This information can be used as a reference when interpreting circulating levels of these biomarkers in relation to the extent and localisation of CNS-damaging processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-022-00935-6.
format Online
Article
Text
id pubmed-9241296
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-92412962022-06-30 Distribution of five clinically important neuroglial proteins in the human brain Sjölin, Karl Kultima, Kim Larsson, Anders Freyhult, Eva Zjukovskaja, Christina Alkass, Kanar Burman, Joachim Mol Brain Research Glial fibrillary acidic protein (GFAP), myelin basic protein (MBP), neurofilament light chain (NFL), tau and ubiquitin carboxy-terminal hydrolase L1 (UCHL1) are five neuroglial proteins that are used as CSF or blood biomarkers of tissue damage in the nervous system. There is incomplete knowledge of how the concentration of these proteins differs between anatomical regions in the CNS as previous studies have focused on gene expression or non-quantitative protein analyses, limiting the interpretability of these biomarkers. The purpose of this study was to create a map of the tissue content of these proteins in different regions of the CNS. The concentrations of the investigated proteins were determined with ELISA in post mortem tissue homogenates from 17 selected anatomical regions in the CNS from ten deceased donors aged 24 to 50 years. When appropriate, the protein concentrations were adjusted for post-mortem interval. In total, 168 tissue samples were analysed. There was a substantial variation in the concentrations of GFAP, MBP, NFL, tau and UCHL1 between different CNS regions. Highly myelinated areas of the CNS had tenfold higher MBP concentration than cerebral cortex, whereas tau showed an inverse pattern. GFAP, NFL and tau displayed an anteroposterior gradient in cerebral white matter. The cerebellum had low concentrations of all the investigated proteins. In conclusion, the tissue concentrations of GFAP, MBP, NFL, tau and UCHL1 were determined throughout the CNS. This information can be used as a reference when interpreting circulating levels of these biomarkers in relation to the extent and localisation of CNS-damaging processes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-022-00935-6. BioMed Central 2022-06-29 /pmc/articles/PMC9241296/ /pubmed/35765081 http://dx.doi.org/10.1186/s13041-022-00935-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Sjölin, Karl
Kultima, Kim
Larsson, Anders
Freyhult, Eva
Zjukovskaja, Christina
Alkass, Kanar
Burman, Joachim
Distribution of five clinically important neuroglial proteins in the human brain
title Distribution of five clinically important neuroglial proteins in the human brain
title_full Distribution of five clinically important neuroglial proteins in the human brain
title_fullStr Distribution of five clinically important neuroglial proteins in the human brain
title_full_unstemmed Distribution of five clinically important neuroglial proteins in the human brain
title_short Distribution of five clinically important neuroglial proteins in the human brain
title_sort distribution of five clinically important neuroglial proteins in the human brain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241296/
https://www.ncbi.nlm.nih.gov/pubmed/35765081
http://dx.doi.org/10.1186/s13041-022-00935-6
work_keys_str_mv AT sjolinkarl distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain
AT kultimakim distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain
AT larssonanders distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain
AT freyhulteva distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain
AT zjukovskajachristina distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain
AT alkasskanar distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain
AT burmanjoachim distributionoffiveclinicallyimportantneuroglialproteinsinthehumanbrain