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Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()

In the majority of studies using primary cultures of myoblasts, the cells are maintained at ambient oxygen tension (21% O(2)), despite the fact that physiological O(2) at the tissue level in vivo is much lower (~1–5% O(2)). We hypothesized that the cellular response in presence of high oxygen concen...

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Autores principales: Konigsberg, M., Pérez, V.I., Ríos, C., Liu, Y., Lee, S., Shi, Y., Van Remmen, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814963/
https://www.ncbi.nlm.nih.gov/pubmed/24191243
http://dx.doi.org/10.1016/j.redox.2013.09.004
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author Konigsberg, M.
Pérez, V.I.
Ríos, C.
Liu, Y.
Lee, S.
Shi, Y.
Van Remmen, H.
author_facet Konigsberg, M.
Pérez, V.I.
Ríos, C.
Liu, Y.
Lee, S.
Shi, Y.
Van Remmen, H.
author_sort Konigsberg, M.
collection PubMed
description In the majority of studies using primary cultures of myoblasts, the cells are maintained at ambient oxygen tension (21% O(2)), despite the fact that physiological O(2) at the tissue level in vivo is much lower (~1–5% O(2)). We hypothesized that the cellular response in presence of high oxygen concentration might be particularly important in studies comparing energetic function or oxidative stress in cells isolated from young versus old animals. To test this, we asked whether oxygen tension plays a role in mitochondrial bioenergetics (oxygen consumption, glycolysis and fatty acid oxidation) or oxidative damage to proteins (protein disulfides, carbonyls and aggregates) in myoblast precursor cells (MPCs) isolated from young (3–4 m) and old (29–30 m) C57BL/6 mice. MPCs were grown under physiological (3%) or ambient (21%) O(2) for two weeks prior to exposure to an acute oxidative insult (H(2)O(2)). Our results show significantly higher basal mitochondrial respiration in young versus old MPCs, an increase in basal respiration in young MPCs maintained at 3% O(2) compared to cells maintained at 21% O(2), and a shift toward glycolytic metabolism in old MPCs grown at 21% O(2). H(2)O(2) treatment significantly reduced respiration in old MPCs grown at 3% O(2) but did not further repress respiration at 21% O(2) in old MPCs. Oxidative damage to protein was higher in cells maintained at 21% O(2) and increased in response to H(2)O(2) in old MPCs. These data underscore the importance of understanding the effect of ambient oxygen tension in cell culture studies, in particular studies measuring oxidative damage and mitochondrial function.
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spelling pubmed-38149632013-11-04 Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells() Konigsberg, M. Pérez, V.I. Ríos, C. Liu, Y. Lee, S. Shi, Y. Van Remmen, H. Redox Biol Research Paper In the majority of studies using primary cultures of myoblasts, the cells are maintained at ambient oxygen tension (21% O(2)), despite the fact that physiological O(2) at the tissue level in vivo is much lower (~1–5% O(2)). We hypothesized that the cellular response in presence of high oxygen concentration might be particularly important in studies comparing energetic function or oxidative stress in cells isolated from young versus old animals. To test this, we asked whether oxygen tension plays a role in mitochondrial bioenergetics (oxygen consumption, glycolysis and fatty acid oxidation) or oxidative damage to proteins (protein disulfides, carbonyls and aggregates) in myoblast precursor cells (MPCs) isolated from young (3–4 m) and old (29–30 m) C57BL/6 mice. MPCs were grown under physiological (3%) or ambient (21%) O(2) for two weeks prior to exposure to an acute oxidative insult (H(2)O(2)). Our results show significantly higher basal mitochondrial respiration in young versus old MPCs, an increase in basal respiration in young MPCs maintained at 3% O(2) compared to cells maintained at 21% O(2), and a shift toward glycolytic metabolism in old MPCs grown at 21% O(2). H(2)O(2) treatment significantly reduced respiration in old MPCs grown at 3% O(2) but did not further repress respiration at 21% O(2) in old MPCs. Oxidative damage to protein was higher in cells maintained at 21% O(2) and increased in response to H(2)O(2) in old MPCs. These data underscore the importance of understanding the effect of ambient oxygen tension in cell culture studies, in particular studies measuring oxidative damage and mitochondrial function. Elsevier 2013-09-27 /pmc/articles/PMC3814963/ /pubmed/24191243 http://dx.doi.org/10.1016/j.redox.2013.09.004 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Konigsberg, M.
Pérez, V.I.
Ríos, C.
Liu, Y.
Lee, S.
Shi, Y.
Van Remmen, H.
Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
title Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
title_full Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
title_fullStr Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
title_full_unstemmed Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
title_short Effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
title_sort effect of oxygen tension on bioenergetics and proteostasis in young and old myoblast precursor cells()
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814963/
https://www.ncbi.nlm.nih.gov/pubmed/24191243
http://dx.doi.org/10.1016/j.redox.2013.09.004
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