dc.contributor.author
Farré Ventura, Ramon
dc.contributor.author
Almendros López, Isaac
dc.contributor.author
Montserrat Canal, José Ma.
dc.contributor.author
Gozal, David
dc.contributor.author
Navajas Navarro, Daniel
dc.date.issued
2019-12-09T16:58:41Z
dc.date.issued
2019-12-09T16:58:41Z
dc.date.issued
2018-12-13
dc.date.issued
2019-12-09T16:58:42Z
dc.identifier
https://hdl.handle.net/2445/146317
dc.description.abstract
Gas partial pressures within the cell microenvironment are one of the key modulators of cell pathophysiology. Indeed, respiratory gases (O2 and CO2) are usually altered in respiratory diseases and gasotransmitters (CO, NO, H2S) have been proposed as potential therapeutic agents. Investigating the pathophysiology of respiratory diseases in vitro mandates that cultured cells are subjected to gas partial pressures similar to those experienced by each cell type in its native microenvironment. For instance, O2 partial pressures range from ∼13% in the arterial endothelium to values as low as 2-5% in cells of other healthy tissues and to less than 1% in solid tumor cells, clearly much lower values than those used in conventional cell culture research settings (∼19%). Moreover, actual cell O2 partial pressure in vivo changes with time, at considerably different timescales as illustrated by tumors, sleep apnea, or mechanical ventilation. Unfortunately, the conventional approach to modify gas concentrations at the above culture medium precludes the tight and exact control of intra-cellular gas levels to realistically mimic the natural cell microenvironment. Interestingly, well-controlled cellular application of gas partial pressures is currently possible through commercially available silicone-like material (PDMS) membranes, which are biocompatible and have a high permeability to gases. Cells are seeded on one side of the membrane and tailored gas concentrations are circulated on the other side of the membrane. Using thin membranes (50-100 μm) the value of gas concentration is instantaneously (<0.5 s) transmitted to the cell microenvironment. As PDMS is transparent, cells can be concurrently observed by conventional or advanced microscopy. This procedure can be implemented in specific-purpose microfluidic devices and in settings that do not require expensive or complex technologies, thus making the procedure readily implementable in any cell biology laboratory. This review describes the gas composition requirements for a cell culture in respiratory research, the limitations of current experimental settings, and also suggests new approaches to better control gas partial pressures in a cell culture.
dc.format
application/pdf
dc.publisher
Frontiers Media
dc.relation
Reproducció del document publicat a: https://doi.org/10.3389/fphys.2018.01803
dc.relation
Frontiers in Physiology, 2018, vol. 9, p. 1803
dc.relation
https://doi.org/10.3389/fphys.2018.01803
dc.rights
cc-by (c) Farré Ventura, Ramon et al., 2018
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biomedicina)
dc.subject
Síndromes d'apnea del son
dc.subject
Malalties pulmonars obstructives cròniques
dc.subject
Respiració artificial
dc.subject
Sleep apnea syndromes
dc.subject
Chronic obstructive pulmonary diseases
dc.subject
Artificial respiration
dc.title
Gas partial pressure in cultured cells: patho-physiological importance and methodological approaches
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion