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Difference between revisions of "Boada 2004 Free Radical Biol Med"

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{{Publication
{{Publication
|title=Boada J, Cuesta E, Perales JC, Roig T, Bermudez J (2004) Glutathione content and adaptation to endogenously induced energy depletion in Mv1Lu cells. Free Radic Biol Med 15: 1555-1565.
|title=Boada J, Cuesta E, Perales JC, Roig T, Bermudez J (2004) Glutathione content and adaptation to endogenously induced energy depletion in Mv1Lu cells. Free Radic Biol Med 15:1555-65.
|info=[http://www.ncbi.nlm.nih.gov/pubmed/15182857 PMID: 15182857]
|info=[http://www.ncbi.nlm.nih.gov/pubmed/15182857 PMID: 15182857]
|authors=Boada J, Cuesta E, Perales JC, Roig T, Bermudez J
|authors=Boada J, Cuesta E, Perales JC, Roig T, Bermudez J
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|abstract=Transfection of genes that code for enzymes of energy metabolism provides alternative models to study the adaptive response to energy restriction induced by endogenous changes instead of by unfavorable environmental conditions. Overexpression of the glycolytic enzyme fructose-2,6-bisphosphatase reduced the content of fructose 2,6-bisphosphate, inducing energy limitation in the mink lung epithelial cell line Mv1Lu. This metabolic stress reduced the ATP available in transfected cells by 20%, which downregulated active ion transport and protein turnover. Ion homeostasis and cell function require concomitant reductions in cell membrane ion permeability and protein damage. Our results indicate that glutathione content linked these features of the adaptive response to the endogenously induced metabolic downregulation.
|abstract=Transfection of genes that code for enzymes of energy metabolism provides alternative models to study the adaptive response to energy restriction induced by endogenous changes instead of by unfavorable environmental conditions. Overexpression of the glycolytic enzyme fructose-2,6-bisphosphatase reduced the content of fructose 2,6-bisphosphate, inducing energy limitation in the mink lung epithelial cell line Mv1Lu. This metabolic stress reduced the ATP available in transfected cells by 20%, which downregulated active ion transport and protein turnover. Ion homeostasis and cell function require concomitant reductions in cell membrane ion permeability and protein damage. Our results indicate that glutathione content linked these features of the adaptive response to the endogenously induced metabolic downregulation.
|keywords=Metabolic stress, 6-Phosphofructo-2-kinase/fructose-2,6-bisphosphatase, Fructose 2,6-bisphosphate, Glutathione, Na+–K+ pump, Potassium channels, Protein synthesis, Free radicals
|keywords=Metabolic stress, 6-Phosphofructo-2-kinase/fructose-2,6-bisphosphatase, Fructose 2,6-bisphosphate, Glutathione, Na+–K+ pump, Potassium channels, Protein synthesis, Free radicals
|mipnetlab=ES_Barcelona_Bermudez MJ
|mipnetlab=ES L'Hospitalet Bermudez MJ, ES Lleida Boada J
}}
}}
{{Labeling
{{Labeling
|injuries=Oxidative stress;RONS
|organism=Rat
|tissues=Liver, Other cell lines
|preparations=Intact cells
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|injuries=RONS; Oxidative Stress
|organism=Rat
|tissues=Liver
|model cell lines=Other cell lines
|preparations=Intact Cell; Cultured; Primary
}}
}}

Latest revision as of 17:12, 19 February 2018

Publications in the MiPMap
Boada J, Cuesta E, Perales JC, Roig T, Bermudez J (2004) Glutathione content and adaptation to endogenously induced energy depletion in Mv1Lu cells. Free Radic Biol Med 15:1555-65.

Β» PMID: 15182857

Boada J, Cuesta E, Perales JC, Roig T, Bermudez J (2004) Free Radic Biol Med

Abstract: Transfection of genes that code for enzymes of energy metabolism provides alternative models to study the adaptive response to energy restriction induced by endogenous changes instead of by unfavorable environmental conditions. Overexpression of the glycolytic enzyme fructose-2,6-bisphosphatase reduced the content of fructose 2,6-bisphosphate, inducing energy limitation in the mink lung epithelial cell line Mv1Lu. This metabolic stress reduced the ATP available in transfected cells by 20%, which downregulated active ion transport and protein turnover. Ion homeostasis and cell function require concomitant reductions in cell membrane ion permeability and protein damage. Our results indicate that glutathione content linked these features of the adaptive response to the endogenously induced metabolic downregulation. β€’ Keywords: Metabolic stress, 6-Phosphofructo-2-kinase/fructose-2, 6-bisphosphatase, Fructose 2, 6-bisphosphate, Glutathione, Na+–K+ pump, Potassium channels, Protein synthesis, Free radicals

β€’ O2k-Network Lab: ES L'Hospitalet Bermudez MJ, ES Lleida Boada J


Labels:

Stress:Oxidative stress;RONS  Organism: Rat  Tissue;cell: Liver, Other cell lines  Preparation: Intact cells 



HRR: Oxygraph-2k