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Adrenoceptor Expression during Intervertebral Disc Degeneration

Healthy and degenerating intervertebral discs (IVDs) are innervated by sympathetic nerves, however, adrenoceptor (AR) expression and functionality have never been investigated systematically. Therefore, AR gene expression was analyzed in both tissue and isolated cells from degenerated human IVDs. Fu...

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Autores principales: Kupka, Johannes, Kohler, Annika, El Bagdadi, Karima, Bostelmann, Richard, Brenneis, Marco, Fleege, Christoph, Chan, Danny, Zaucke, Frank, Meurer, Andrea, Rickert, Marcus, Jenei-Lanzl, Zsuzsa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139977/
https://www.ncbi.nlm.nih.gov/pubmed/32197418
http://dx.doi.org/10.3390/ijms21062085
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author Kupka, Johannes
Kohler, Annika
El Bagdadi, Karima
Bostelmann, Richard
Brenneis, Marco
Fleege, Christoph
Chan, Danny
Zaucke, Frank
Meurer, Andrea
Rickert, Marcus
Jenei-Lanzl, Zsuzsa
author_facet Kupka, Johannes
Kohler, Annika
El Bagdadi, Karima
Bostelmann, Richard
Brenneis, Marco
Fleege, Christoph
Chan, Danny
Zaucke, Frank
Meurer, Andrea
Rickert, Marcus
Jenei-Lanzl, Zsuzsa
author_sort Kupka, Johannes
collection PubMed
description Healthy and degenerating intervertebral discs (IVDs) are innervated by sympathetic nerves, however, adrenoceptor (AR) expression and functionality have never been investigated systematically. Therefore, AR gene expression was analyzed in both tissue and isolated cells from degenerated human IVDs. Furthermore, human IVD samples and spine sections of wildtype mice (WT) and of a mouse line that develops spontaneous IVD degeneration (IVDD, in SM/J mice) were stained for ARs and extracellular matrix (ECM) components. In IVD homogenates and cells α1a-, α1b-, α2a-, α2b-, α2c-, β1-, and β2-AR genes were expressed. In human sections, β2-AR was detectable, and its localization parallels with ECM alterations. Similarly, in IVDs of WT mice, only β2-AR was expressed, and in IVDs of SM/J mice, β2AR expression was stronger accompanied by increased collagen II, collagen XII, decorin as well as decreased cartilage oligomeric matrix protein expression. In addition, norepinephrine stimulation of isolated human IVD cells induced intracellular signaling via ERK1/2 and PKA. For the first time, the existence and functionality of ARs were demonstrated in IVD tissue samples, suggesting that the sympathicus might play a role in IVDD. Further studies will address relevant cellular mechanisms and thereby help to develop novel therapeutic options for IVDD.
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spelling pubmed-71399772020-04-13 Adrenoceptor Expression during Intervertebral Disc Degeneration Kupka, Johannes Kohler, Annika El Bagdadi, Karima Bostelmann, Richard Brenneis, Marco Fleege, Christoph Chan, Danny Zaucke, Frank Meurer, Andrea Rickert, Marcus Jenei-Lanzl, Zsuzsa Int J Mol Sci Article Healthy and degenerating intervertebral discs (IVDs) are innervated by sympathetic nerves, however, adrenoceptor (AR) expression and functionality have never been investigated systematically. Therefore, AR gene expression was analyzed in both tissue and isolated cells from degenerated human IVDs. Furthermore, human IVD samples and spine sections of wildtype mice (WT) and of a mouse line that develops spontaneous IVD degeneration (IVDD, in SM/J mice) were stained for ARs and extracellular matrix (ECM) components. In IVD homogenates and cells α1a-, α1b-, α2a-, α2b-, α2c-, β1-, and β2-AR genes were expressed. In human sections, β2-AR was detectable, and its localization parallels with ECM alterations. Similarly, in IVDs of WT mice, only β2-AR was expressed, and in IVDs of SM/J mice, β2AR expression was stronger accompanied by increased collagen II, collagen XII, decorin as well as decreased cartilage oligomeric matrix protein expression. In addition, norepinephrine stimulation of isolated human IVD cells induced intracellular signaling via ERK1/2 and PKA. For the first time, the existence and functionality of ARs were demonstrated in IVD tissue samples, suggesting that the sympathicus might play a role in IVDD. Further studies will address relevant cellular mechanisms and thereby help to develop novel therapeutic options for IVDD. MDPI 2020-03-18 /pmc/articles/PMC7139977/ /pubmed/32197418 http://dx.doi.org/10.3390/ijms21062085 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kupka, Johannes
Kohler, Annika
El Bagdadi, Karima
Bostelmann, Richard
Brenneis, Marco
Fleege, Christoph
Chan, Danny
Zaucke, Frank
Meurer, Andrea
Rickert, Marcus
Jenei-Lanzl, Zsuzsa
Adrenoceptor Expression during Intervertebral Disc Degeneration
title Adrenoceptor Expression during Intervertebral Disc Degeneration
title_full Adrenoceptor Expression during Intervertebral Disc Degeneration
title_fullStr Adrenoceptor Expression during Intervertebral Disc Degeneration
title_full_unstemmed Adrenoceptor Expression during Intervertebral Disc Degeneration
title_short Adrenoceptor Expression during Intervertebral Disc Degeneration
title_sort adrenoceptor expression during intervertebral disc degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139977/
https://www.ncbi.nlm.nih.gov/pubmed/32197418
http://dx.doi.org/10.3390/ijms21062085
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