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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.zeige mehrzeige weniger

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Metadaten
Verfasserangaben: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
Titel des übergeordneten Werks (Englisch):European cells & materials
Untertitel (Englisch):how intervertebral disc cells respond to altered osmolarity
Verlag:Ao research institute davos-Ari
Verlagsort:Davos
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:19.11.2018
Erscheinungsjahr:2018
Datum der Freischaltung:08.11.2021
Freies Schlagwort / Tag:Intervertebral disc degeneration; aquaporin; degenerative disc disease; hyper-osmolarity; hypo-osmolarity; inflammatory; osmolarity; osmotic; tonicity-responsive enhancer binding protein; transient receptor potential channel
Band:36
Seitenanzahl:20
Erste Seite:231
Letzte Seite:250
Organisationseinheiten:Humanwissenschaftliche Fakultät / Strukturbereich Kognitionswissenschaften / Department Sport- und Gesundheitswissenschaften
DDC-Klassifikation:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Peer Review:Referiert
Publikationsweg:Open Access / Green Open-Access
DOAJ gelistet
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