Mueller 2012 PLoS One: Difference between revisions
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{{Publication | {{Publication | ||
|title=Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B (2012) Functional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells. PLoS One 7:e52367. | |title=Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B (2012) Functional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells. PLoS One 7:e52367. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/23300652 PMID: 23300652] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/23300652 PMID: 23300652 Open Access] | ||
|authors=Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B | |authors=Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B | ||
|year=2012 | |year=2012 | ||
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The results of this study show that functional differences exist between HEK293 cybrid cells which differ in mitochondrial genomic background. | The results of this study show that functional differences exist between HEK293 cybrid cells which differ in mitochondrial genomic background. | ||
|mipnetlab=AT Salzburg Sperl W | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
|area=Respiration, mtDNA;mt-genetics | |area=Respiration, mtDNA;mt-genetics | ||
|injuries=Oxidative stress;RONS | |||
|organism=Human | |organism=Human | ||
|tissues=Blood cells | |tissues=Blood cells, HEK | ||
|preparations=Intact cells | |preparations=Intact cells | ||
|couplingstates=OXPHOS | |couplingstates=OXPHOS | ||
}} | }} |
Latest revision as of 14:16, 26 March 2018
Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B (2012) Functional differences between mitochondrial haplogroup T and haplogroup H in HEK293 cybrid cells. PLoS One 7:e52367. |
Mueller EE, Brunner SM, Mayr JA, Stanger O, Sperl W, Kofler B (2012) PLoS One
Abstract: Epidemiological case-control studies have revealed associations between mitochondrial haplogroups and the onset and/or progression of various multifactorial diseases. For instance, mitochondrial haplogroup T was previously shown to be associated with vascular diseases, including coronary artery disease and diabetic retinopathy. In contrast, haplogroup H, the most frequent haplogroup in Europe, is often found to be more prevalent in healthy control subjects than in patient study groups. However, justifications for the assumption that haplogroups are functionally distinct are rare. Therefore, we attempted to compare differences in mitochondrial function between haplogroup H and T cybrids.
Mitochondrial haplogroup H and T cybrids were generated by fusion of HEK293 cells devoid of mitochondrial DNA with isolated thrombocytes of individuals with the respective haplogroups. These cybrid cells were analyzed for oxidative phosphorylation (OXPHOS) enzyme activities, mitochondrial DNA (mtDNA) copy number, growth rate and susceptibility to reactive oxygen species (ROS). We observed that haplogroup T cybrids have higher survival rate when challenged with hydrogen peroxide, indicating a higher capability to cope with oxidative stress.
The results of this study show that functional differences exist between HEK293 cybrid cells which differ in mitochondrial genomic background.
โข O2k-Network Lab: AT Salzburg Sperl W
Labels: MiParea: Respiration, mtDNA;mt-genetics
Stress:Oxidative stress;RONS Organism: Human Tissue;cell: Blood cells, HEK Preparation: Intact cells
Coupling state: OXPHOS