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The Effects of Cholera Toxin on Cellular Energy Metabolism

Multianalyte microphysiometry, a real-time instrument for simultaneous measurement of metabolic analytes in a microfluidic environment, was used to explore the effects of cholera toxin (CTx). Upon exposure of CTx to PC-12 cells, anaerobic respiration was triggered, measured as increases in acid and...

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Autores principales: Snider, Rachel M., McKenzie, Jennifer R., Kraft, Lewis, Kozlov, Eugene, Wikswo, John P., Cliffel, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153216/
https://www.ncbi.nlm.nih.gov/pubmed/22069603
http://dx.doi.org/10.3390/toxins2040632
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author Snider, Rachel M.
McKenzie, Jennifer R.
Kraft, Lewis
Kozlov, Eugene
Wikswo, John P.
Cliffel, David E.
author_facet Snider, Rachel M.
McKenzie, Jennifer R.
Kraft, Lewis
Kozlov, Eugene
Wikswo, John P.
Cliffel, David E.
author_sort Snider, Rachel M.
collection PubMed
description Multianalyte microphysiometry, a real-time instrument for simultaneous measurement of metabolic analytes in a microfluidic environment, was used to explore the effects of cholera toxin (CTx). Upon exposure of CTx to PC-12 cells, anaerobic respiration was triggered, measured as increases in acid and lactate production and a decrease in the oxygen uptake. We believe the responses observed are due to a CTx-induced activation of adenylate cyclase, increasing cAMP production and resulting in a switch to anaerobic respiration. Inhibitors (H-89, brefeldin A) and stimulators (forskolin) of cAMP were employed to modulate the CTx-induced cAMP responses. The results of this study show the utility of multianalyte microphysiometry to quantitatively determine the dynamic metabolic effects of toxins and affected pathways.
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spelling pubmed-31532162011-11-08 The Effects of Cholera Toxin on Cellular Energy Metabolism Snider, Rachel M. McKenzie, Jennifer R. Kraft, Lewis Kozlov, Eugene Wikswo, John P. Cliffel, David E. Toxins (Basel) Article Multianalyte microphysiometry, a real-time instrument for simultaneous measurement of metabolic analytes in a microfluidic environment, was used to explore the effects of cholera toxin (CTx). Upon exposure of CTx to PC-12 cells, anaerobic respiration was triggered, measured as increases in acid and lactate production and a decrease in the oxygen uptake. We believe the responses observed are due to a CTx-induced activation of adenylate cyclase, increasing cAMP production and resulting in a switch to anaerobic respiration. Inhibitors (H-89, brefeldin A) and stimulators (forskolin) of cAMP were employed to modulate the CTx-induced cAMP responses. The results of this study show the utility of multianalyte microphysiometry to quantitatively determine the dynamic metabolic effects of toxins and affected pathways. Molecular Diversity Preservation International 2010-04-08 /pmc/articles/PMC3153216/ /pubmed/22069603 http://dx.doi.org/10.3390/toxins2040632 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Snider, Rachel M.
McKenzie, Jennifer R.
Kraft, Lewis
Kozlov, Eugene
Wikswo, John P.
Cliffel, David E.
The Effects of Cholera Toxin on Cellular Energy Metabolism
title The Effects of Cholera Toxin on Cellular Energy Metabolism
title_full The Effects of Cholera Toxin on Cellular Energy Metabolism
title_fullStr The Effects of Cholera Toxin on Cellular Energy Metabolism
title_full_unstemmed The Effects of Cholera Toxin on Cellular Energy Metabolism
title_short The Effects of Cholera Toxin on Cellular Energy Metabolism
title_sort effects of cholera toxin on cellular energy metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3153216/
https://www.ncbi.nlm.nih.gov/pubmed/22069603
http://dx.doi.org/10.3390/toxins2040632
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