The aggressiveness of succinate dehydrogenase subunit B-deficient chromaffin cells is reduced when their bioelectrical properties are restored by glibenclamide
Jazyk angličtina Země Anglie, Velká Británie Médium electronic-print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
37493200
DOI
10.1530/erc-23-0167
PII: e230167
Knihovny.cz E-zdroje
- Klíčová slova
- ATP-sensitive potassium channels, bioelectrical properties, glibenclamide, pheochromocytoma/paraganglioma, succinate dehydrogenase,
- MeSH
- adenosintrifosfát MeSH
- chromafinní buňky * metabolismus patologie MeSH
- feochromocytom * genetika MeSH
- glibenklamid farmakologie MeSH
- lidé MeSH
- nádory nadledvin * genetika MeSH
- paragangliom * genetika MeSH
- sukcinátdehydrogenasa genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adenosintrifosfát MeSH
- glibenklamid MeSH
- sukcinátdehydrogenasa MeSH
Pheochromocytomas/paragangliomas (PPGLs) are neuroendocrine tumours, mostly resulting from mutations in predisposing genes. Mutations of succinate dehydrogenase (SDH) subunit B (SDHB) are associated with high probability of metastatic disease. Since bioelectrical properties and signalling in cancer are an emerging field, we investigated the metabolic, functional and electrophysiological characteristics in human succinate dehydrogenase subunit B (SDHB)-deficient pheochromocytoma cells. These cells exhibited reduced SDH function with elevated succinate-to-fumarate ratio and reduced intracellular ATP levels. The analysis of membrane passive properties revealed a more hyperpolarized membrane potential and a lower cell capacitance of SDHB-deficient cells compared to the parental ones. These bioelectrical changes were associated with reduced proliferation and adhesion capacity of SDHB-deficient cells. Only in SDHB-deficient cells, we also observed an increased amplitude of potassium currents suggesting an activation of ATP-sensitive potassium channels (KATP). Indeed, exposure of the SDHB-deficient cells to glibenclamide, a specific KATP inhibitor, or to ATP caused normalization of potassium current features and altered proliferation and adhesion. In this work, we show for the first time that reduced intracellular ATP levels in SDHB-deficient chromaffin cells impaired cell bioelectrical properties, which, in turn, are associated with an increased cell aggressiveness. Moreover, we first ever demonstrated that glibenclamide not only reduced the outward potassium currents in SDHB-deficient cells but increased their growth capacity, reduced their ability to migrate and shifted their phenotype towards one more similar to that of parental one.
Center of Excellence Florence Italy
Centro di Ricerca e Innovazione sulle Patologie Surrenaliche AOU Careggi Florence Italy
Department Experimental and Clinical Biomedical Sciences University of Florence Florence Italy
Department Experimental and Clinical Medicine University of Florence Florence Italy
Department of Experimental and Clinical Medicine Imaging Platform University of Florence Italy
Faculty of Science and 1st Medical Faculty Charles University Prague Czech Republic
Institute of Biotechnology Czech Academy of Sciences Prague West Czech Republic
School of Pharmacy and Medical Science Griffith University Southport Queensland Australia
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