2017-06-14T14:48:33Z
2017-06-14T14:48:33Z
2016-07-29
2017-06-14T14:48:33Z
Intermittent hypoxia (IH), a hallmark of obstructive sleep apnea (OSA), plays a critical role in the pathogenesis of OSA-associated morbidities, especially in the cardiovascular and respiratory systems. Oxidative stress and inflammation induced by IH are suggested as main contributors of end-organ dysfunction in OSA patients and animal models. Since the molecular mechanisms underlying these in vivo pathological responses remain poorly understood, implementation of experimental in vitro cell-based systems capable of inducing high-frequency IH would be highly desirable. Here, we describe the design, fabrication, and validation of a versatile chip for subjecting cultured cells to fast changes in gas partial pressure and to cyclic stretch. The chip is fabricated with polydimethylsiloxane (PDMS) and consists of a cylindrical well-covered by a thin membrane. Cells cultured on top of the membrane can be subjected to fast changes in oxygen concentration (equilibrium time similar to 6 s). Moreover, cells can be subjected to cyclic stretch at cardiac or respiratory frequencies independently or simultaneously. Rat bone marrow-derived mesenchymal stem cells (MSCs) exposed to IH mimicking OSA and cyclic stretch at cardiac frequencies revealed that hypoxia-inducible factor 1 alpha (HIF-1 alpha) expression was increased in response to both stimuli. Thus, the chip provides a versatile tool for the study of cellular responses to cyclical hypoxia and stretch.
Article
Published version
English
Síndromes d'apnea del son; Oxigen en l'organisme; Respiració; Sleep apnea syndromes; Oxygen in the body; Respiration
Frontiers Media
Reproducció del document publicat a: https://doi.org/10.3339/fphys.2016.00319
Frontiers in Physiology, 2016, vol. 7, num. 319
https://doi.org/10.3339/fphys.2016.00319
cc-by (c) Campillo, Noelia et al., 2016
http://creativecommons.org/licenses/by/3.0/es