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Endothelial cells are an important source of BDNF in rat skeletal muscle

BDNF (brain-derived neurotrophic factor) is present in skeletal muscle, controlling muscular metabolism, strength and regeneration processes. However, there is no consensus on BDNF cellular source. Furthermore, while endothelial tissue expresses BDNF in large amount, whether endothelial cells inside...

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Autores principales: Cefis, Marina, Chaney, Remi, Quirié, Aurore, Santini, Clélia, Marie, Christine, Garnier, Philippe, Prigent-Tessier, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748777/
https://www.ncbi.nlm.nih.gov/pubmed/35013359
http://dx.doi.org/10.1038/s41598-021-03740-8
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author Cefis, Marina
Chaney, Remi
Quirié, Aurore
Santini, Clélia
Marie, Christine
Garnier, Philippe
Prigent-Tessier, Anne
author_facet Cefis, Marina
Chaney, Remi
Quirié, Aurore
Santini, Clélia
Marie, Christine
Garnier, Philippe
Prigent-Tessier, Anne
author_sort Cefis, Marina
collection PubMed
description BDNF (brain-derived neurotrophic factor) is present in skeletal muscle, controlling muscular metabolism, strength and regeneration processes. However, there is no consensus on BDNF cellular source. Furthermore, while endothelial tissue expresses BDNF in large amount, whether endothelial cells inside muscle expressed BDNF has never been explored. The aim of the present study was to provide a comprehensive analysis of BDNF localization in rat skeletal muscle. Cellular localization of BDNF and activated Tropomyosin-related kinase B (TrkB) receptors was studied by immunohistochemical analysis on soleus (SOL) and gastrocnemius (GAS). BDNF and activated TrkB levels were also measured in muscle homogenates using Western blot analysis and/or Elisa tests. The results revealed BDNF immunostaining in all cell types examined with a prominent staining in endothelial cells and a stronger staining in type II than type I muscular fibers. Endothelial cells but not other cells displayed easily detectable activated TrkB receptor expression. Levels of BDNF and activated TrkB receptors were higher in SOL than GAS. In conclusion, endothelial cells are an important and still unexplored source of BDNF present in skeletal muscle. Endothelial BDNF expression likely explains why oxidative muscle exhibits higher BDNF levels than glycolytic muscle despite higher the BDNF expression by type II fibers.
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spelling pubmed-87487772022-01-11 Endothelial cells are an important source of BDNF in rat skeletal muscle Cefis, Marina Chaney, Remi Quirié, Aurore Santini, Clélia Marie, Christine Garnier, Philippe Prigent-Tessier, Anne Sci Rep Article BDNF (brain-derived neurotrophic factor) is present in skeletal muscle, controlling muscular metabolism, strength and regeneration processes. However, there is no consensus on BDNF cellular source. Furthermore, while endothelial tissue expresses BDNF in large amount, whether endothelial cells inside muscle expressed BDNF has never been explored. The aim of the present study was to provide a comprehensive analysis of BDNF localization in rat skeletal muscle. Cellular localization of BDNF and activated Tropomyosin-related kinase B (TrkB) receptors was studied by immunohistochemical analysis on soleus (SOL) and gastrocnemius (GAS). BDNF and activated TrkB levels were also measured in muscle homogenates using Western blot analysis and/or Elisa tests. The results revealed BDNF immunostaining in all cell types examined with a prominent staining in endothelial cells and a stronger staining in type II than type I muscular fibers. Endothelial cells but not other cells displayed easily detectable activated TrkB receptor expression. Levels of BDNF and activated TrkB receptors were higher in SOL than GAS. In conclusion, endothelial cells are an important and still unexplored source of BDNF present in skeletal muscle. Endothelial BDNF expression likely explains why oxidative muscle exhibits higher BDNF levels than glycolytic muscle despite higher the BDNF expression by type II fibers. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748777/ /pubmed/35013359 http://dx.doi.org/10.1038/s41598-021-03740-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 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/) .
spellingShingle Article
Cefis, Marina
Chaney, Remi
Quirié, Aurore
Santini, Clélia
Marie, Christine
Garnier, Philippe
Prigent-Tessier, Anne
Endothelial cells are an important source of BDNF in rat skeletal muscle
title Endothelial cells are an important source of BDNF in rat skeletal muscle
title_full Endothelial cells are an important source of BDNF in rat skeletal muscle
title_fullStr Endothelial cells are an important source of BDNF in rat skeletal muscle
title_full_unstemmed Endothelial cells are an important source of BDNF in rat skeletal muscle
title_short Endothelial cells are an important source of BDNF in rat skeletal muscle
title_sort endothelial cells are an important source of bdnf in rat skeletal muscle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748777/
https://www.ncbi.nlm.nih.gov/pubmed/35013359
http://dx.doi.org/10.1038/s41598-021-03740-8
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