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Osmosensing, osmosignalling and inflammation

  • Intervertebral disc (IVD) cells are naturally exposed to high osmolarity and complex mechanical loading, which drive microenvironmental osmotic changes. Age- and degeneration-induced degradation of the IVD’s extracellular matrix causes osmotic imbalance, which, together with an altered function of cellular receptors and signalling pathways, instigates local osmotic stress. Cellular responses to osmotic stress include osmoadaptation and activation of pro-inflammatory pathways. This review summarises the current knowledge on how IVD cells sense local osmotic changes and translate these signals into physiological or pathophysiological responses, with a focus on inflammation. Furthermore, it discusses the expression and function of putative membrane osmosensors (e.g. solute carrier transporters, transient receptor potential channels, aquaporins and acid-sensing ion channels) and osmosignalling mediators [e.g. tonicity response-element-binding protein/nuclear factor of activated T-cells 5 (TonEBP/NFAT5), nuclear factorIntervertebral disc (IVD) cells are naturally exposed to high osmolarity and complex mechanical loading, which drive microenvironmental osmotic changes. Age- and degeneration-induced degradation of the IVD’s extracellular matrix causes osmotic imbalance, which, together with an altered function of cellular receptors and signalling pathways, instigates local osmotic stress. Cellular responses to osmotic stress include osmoadaptation and activation of pro-inflammatory pathways. This review summarises the current knowledge on how IVD cells sense local osmotic changes and translate these signals into physiological or pathophysiological responses, with a focus on inflammation. Furthermore, it discusses the expression and function of putative membrane osmosensors (e.g. solute carrier transporters, transient receptor potential channels, aquaporins and acid-sensing ion channels) and osmosignalling mediators [e.g. tonicity response-element-binding protein/nuclear factor of activated T-cells 5 (TonEBP/NFAT5), nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB)] in healthy and degenerated IVDs. Finally, an overview of the potential therapeutic targets for modifying osmosensing and osmosignalling in degenerated IVDs is provided.show moreshow less

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Author details:Aleksandra SadowskaORCiD, Takuya KamedaORCiD, Olga KrupkovaORCiDGND, Karin Wuertz-KozakORCiDGND
DOI:https://doi.org/10.22203/eCM.v036a17
ISSN:1473-2262
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/30452080
Title of parent work (English):European cells & materials
Subtitle (English):how intervertebral disc cells respond to altered osmolarity
Publisher:Ao research institute davos-Ari
Place of publishing:Davos
Publication type:Article
Language:English
Date of first publication:2018/11/19
Publication year:2018
Release date:2021/11/08
Tag:Intervertebral disc degeneration; aquaporin; degenerative disc disease; hyper-osmolarity; hypo-osmolarity; inflammatory; osmolarity; osmotic; tonicity-responsive enhancer binding protein; transient receptor potential channel
Volume:36
Number of pages:20
First page:231
Last Page:250
Organizational units:Humanwissenschaftliche Fakultät / Strukturbereich Kognitionswissenschaften / Department Sport- und Gesundheitswissenschaften
DDC classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Peer review:Referiert
Publishing method:Open Access / Green Open-Access
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