An innovative intermittent hypoxia model for cell cultures allowing fast Po2 oscillations with minimal gas consumption
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28747336
DOI
10.1152/ajpcell.00098.2017
PII: ajpcell.00098.2017
Knihovny.cz E-zdroje
- Klíčová slova
- cell hypertrophy, diabetic nephropathy, fibrosis, mTOR complex 1, microRNAs,
- MeSH
- buněčné kultury * přístrojové vybavení MeSH
- časové faktory MeSH
- design vybavení MeSH
- endoteliální buňky metabolismus MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa metabolismus MeSH
- hematoencefalická bariéra metabolismus MeSH
- hypoxie buňky MeSH
- hypoxie metabolismus MeSH
- kultivační média metabolismus MeSH
- kyslík metabolismus MeSH
- lidé MeSH
- nádorová hypoxie MeSH
- nádorové buněčné linie MeSH
- nádory prsu metabolismus MeSH
- obstrukční spánková apnoe metabolismus MeSH
- plyny MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- faktor 1 indukovatelný hypoxií - podjednotka alfa MeSH
- HIF1A protein, human MeSH Prohlížeč
- kultivační média MeSH
- kyslík MeSH
- plyny MeSH
Performing hypoxia-reoxygenation cycles in cell culture with a cycle duration accurately reflecting what occurs in obstructive sleep apnea (OSA) patients is a difficult but crucial technical challenge. Our goal was to develop a novel device to expose multiple cell culture dishes to intermittent hypoxia (IH) cycles relevant to OSA with limited gas consumption. With gas flows as low as 200 ml/min, our combination of plate holders with gas-permeable cultureware generates rapid normoxia-hypoxia cycles. Cycles alternating 1 min at 20% O2 followed by 1 min at 2% O2 resulted in Po2 values ranging from 124 to 44 mmHg. Extending hypoxic and normoxic phases to 10 min allowed Po2 variations from 120 to 25 mmHg. The volume of culture medium or the presence of cells only modestly affected the Po2 variations. In contrast, the nadir of the hypoxia phase increased when measured at different heights above the membrane. We validated the physiological relevance of this model by showing that hypoxia inducible factor-1α expression was significantly increased by IH exposure in human aortic endothelial cells, murine breast carcinoma (4T1) cells as well as in a blood-brain barrier model (2.5-, 1.5-, and 6-fold increases, respectively). In conclusion, we have established a new device to perform rapid intermittent hypoxia cycles in cell cultures, with minimal gas consumption and the possibility to expose several culture dishes simultaneously. This device will allow functional studies of the consequences of IH and deciphering of the molecular biology of IH at the cellular level using oxygen cycles that are clinically relevant to OSA.
Centre Hospitalier Universitaire Grenoble France
HP2 Laboratory Université Grenoble Alpes Grenoble France
HP2 Laboratory Université Grenoble Alpes Grenoble France;
SMTEC Chemin des Vignes Nyon Switzerland
Université de Lyon and Université Jean Monnet Saint Etienne France
Citace poskytuje Crossref.org
Technical Feasibility and Physiological Relevance of Hypoxic Cell Culture Models