Difference between revisions of "Zhang 2012 Nat Protoc"
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{{Publication | {{Publication | ||
|title=Zhang J, Nuebel E, Wisidagama DR, Setoguchi K, Hong JS, Van Horn CM, Imam SS, Vergnes L, Malone CS, Koehler CM, Teitell MA (2012) Measuring energy metabolism in cultured cells, including human pluripotent stem cells and differentiated cells. Nat Protoc 7: 1068- | |title=Zhang J, Nuebel E, Wisidagama DR, Setoguchi K, Hong JS, Van Horn CM, Imam SS, Vergnes L, Malone CS, Koehler CM, Teitell MA (2012) Measuring energy metabolism in cultured cells, including human pluripotent stem cells and differentiated cells. https://doi.org/10.1038/nprot.2012.048 | ||
|info=Nat Protoc 7: 1068-85. [https://pubmed.ncbi.nlm.nih.gov/22576106/ PMID: 22576106 Open Access] | |||
|authors=Zhang J, Nuebel E, Wisidagama DR, Setoguchi K, Hong JS, Van Horn CM, Imam SS, Vergnes L, Malone CS, Koehler CM, Teitell MA | |authors=Zhang J, Nuebel E, Wisidagama DR, Setoguchi K, Hong JS, Van Horn CM, Imam SS, Vergnes L, Malone CS, Koehler CM, Teitell MA | ||
|year=2012 | |year=2012 | ||
|journal=Nat Protoc | |journal=Nat Protoc | ||
|abstract=Measurements of glycolysis and mitochondrial function are required to quantify energy metabolism in a wide variety of cellular contexts. In human pluripotent stem cells (hPSCs) and their differentiated progeny, this analysis can be challenging because of the unique cell properties, growth conditions and expense required to maintain these cell types. Here we provide protocols for analyzing energy metabolism in hPSCs and their early differentiated progenies that are generally applicable to mature cell types as well. Our approach has revealed distinct energy metabolism profiles used by hPSCs, differentiated cells, a variety of cancer cells and Rho-null cells. The protocols measure or estimate glycolysis on the basis of the extracellular acidification rate, and they measure or estimate oxidative phosphorylation on the basis of the oxygen consumption rate. Assays typically require 3 h after overnight sample preparation. Companion methods are also discussed and provided to aid researchers in developing more sophisticated experimental regimens for extended analyses of cellular bioenergetics. | |abstract=Measurements of glycolysis and mitochondrial function are required to quantify energy metabolism in a wide variety of cellular contexts. In human pluripotent stem cells (hPSCs) and their differentiated progeny, this analysis can be challenging because of the unique cell properties, growth conditions and expense required to maintain these cell types. Here we provide protocols for analyzing energy metabolism in hPSCs and their early differentiated progenies that are generally applicable to mature cell types as well. Our approach has revealed distinct energy metabolism profiles used by hPSCs, differentiated cells, a variety of cancer cells and Rho-null cells. The protocols measure or estimate glycolysis on the basis of the extracellular acidification rate, and they measure or estimate oxidative phosphorylation on the basis of the oxygen consumption rate. Assays typically require 3 h after overnight sample preparation. Companion methods are also discussed and provided to aid researchers in developing more sophisticated experimental regimens for extended analyses of cellular bioenergetics. | ||
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::>> [http://www.nature.com/nprot/journal/v7/n6/fig_tab/nprot.2012.048_T1.html Table: Comparison of common bioenergetic analysis methods] | ::>> [http://www.nature.com/nprot/journal/v7/n6/fig_tab/nprot.2012.048_T1.html Table: Comparison of common bioenergetic analysis methods] | ||
Continue the discussion: [[ | Continue the discussion: [[Talk:Zhang 2012 Nat Protoc]] | ||
::* Discussion: [[Talk:Rogers 2011 PLoS One|XFe for isolated mitochondria - high throughput without high output?]] | ::* Discussion: [[Talk:Rogers 2011 PLoS One|XFe for isolated mitochondria - high throughput without high output?]] | ||
::* | |||
:::* '''Further information''' | |||
::::» [[O2k specifications]] | |||
::::» [[Comparison of respirometric methods]] | |||
::::» [[O2k-Publications: Living cells]] | |||
{{Labeling | |||
|area=Respiration | |||
|tissues=Stem cells | |||
|additional=Comparison of respirometric methods, | |||
PLoSONE2022ace-sce, MitoFit2022QC | |||
}} | |||
Latest revision as of 15:52, 4 June 2022
| Zhang J, Nuebel E, Wisidagama DR, Setoguchi K, Hong JS, Van Horn CM, Imam SS, Vergnes L, Malone CS, Koehler CM, Teitell MA (2012) Measuring energy metabolism in cultured cells, including human pluripotent stem cells and differentiated cells. https://doi.org/10.1038/nprot.2012.048 |
» Nat Protoc 7: 1068-85. PMID: 22576106 Open Access
Zhang J, Nuebel E, Wisidagama DR, Setoguchi K, Hong JS, Van Horn CM, Imam SS, Vergnes L, Malone CS, Koehler CM, Teitell MA (2012) Nat Protoc
Abstract: Measurements of glycolysis and mitochondrial function are required to quantify energy metabolism in a wide variety of cellular contexts. In human pluripotent stem cells (hPSCs) and their differentiated progeny, this analysis can be challenging because of the unique cell properties, growth conditions and expense required to maintain these cell types. Here we provide protocols for analyzing energy metabolism in hPSCs and their early differentiated progenies that are generally applicable to mature cell types as well. Our approach has revealed distinct energy metabolism profiles used by hPSCs, differentiated cells, a variety of cancer cells and Rho-null cells. The protocols measure or estimate glycolysis on the basis of the extracellular acidification rate, and they measure or estimate oxidative phosphorylation on the basis of the oxygen consumption rate. Assays typically require 3 h after overnight sample preparation. Companion methods are also discussed and provided to aid researchers in developing more sophisticated experimental regimens for extended analyses of cellular bioenergetics.
Continue the discussion: Talk:Zhang 2012 Nat Protoc
- Further information
Labels: MiParea: Respiration
Tissue;cell: Stem cells
Comparison of respirometric methods, PLoSONE2022ace-sce, MitoFit2022QC
