Gruening 2011 Cell Metab: Difference between revisions
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{{Publication | {{Publication | ||
|title=Grüning NM, Rinnerthaler M, Bluemlein K, Mülleder M, Wamelink MM, Lehrach H, Jakobs C, Breitenbach M, Ralser M | |title=Grüning NM, Rinnerthaler M, Bluemlein K, Mülleder M, Wamelink MM, Lehrach H, Jakobs C, Breitenbach M, Ralser M (2011) Pyruvate kinase triggers a metabolic feedback loop that controls redox metabolism in respiring cells. Cell Metab 14:415-27. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed?term=21907146 PMID: 21907146 | |info=[http://www.ncbi.nlm.nih.gov/pubmed?term=21907146 PMID: 21907146 Open Access] | ||
|authors= | |authors=Gruening NM, Rinnerthaler M, Bluemlein K, Muelleder M, Wamelink MM, Lehrach H, Jakobs C, Breitenbach M, Ralser M | ||
|year=2011 | |year=2011 | ||
|journal=Cell Metab | |journal=Cell Metab | ||
|abstract=In proliferating cells, a transition from aerobic to anaerobic metabolism is known as the Warburg effect, whose reversal inhibits cancer cell proliferation. Studying its regulator pyruvate kinase (PYK) in yeast, we discovered that central metabolism is self-adapting to synchronize redox metabolism when respiration is activated. Low PYK activity activated yeast respiration. However, levels of reactive oxygen species (ROS) did not increase, and cells gained resistance to oxidants. This adaptation was attributable to accumulation of the PYK substrate phosphoenolpyruvate (PEP). PEP acted as feedback inhibitor of the glycolytic enzyme triosephosphate isomerase (TPI). TPI inhibition stimulated the pentose phosphate pathway, increased antioxidative metabolism, and prevented ROS accumulation. Thus, a metabolic feedback loop, initiated by PYK, mediated by its substrate and acting on TPI, stimulates redox metabolism in respiring cells. Originating from a single catalytic step, this autonomous reconfiguration of central carbon metabolism prevents oxidative stress upon shifts between fermentation and respiration. | |abstract=In proliferating cells, a transition from aerobic to anaerobic metabolism is known as the Warburg effect, whose reversal inhibits cancer cell proliferation. Studying its regulator pyruvate kinase (PYK) in yeast, we discovered that central metabolism is self-adapting to synchronize redox metabolism when respiration is activated. Low PYK activity activated yeast respiration. However, levels of reactive oxygen species (ROS) did not increase, and cells gained resistance to oxidants. This adaptation was attributable to accumulation of the PYK substrate phosphoenolpyruvate (PEP). PEP acted as feedback inhibitor of the glycolytic enzyme triosephosphate isomerase (TPI). TPI inhibition stimulated the pentose phosphate pathway, increased antioxidative metabolism, and prevented ROS accumulation. Thus, a metabolic feedback loop, initiated by PYK, mediated by its substrate and acting on TPI, stimulates redox metabolism in respiring cells. Originating from a single catalytic step, this autonomous reconfiguration of central carbon metabolism prevents oxidative stress upon shifts between fermentation and respiration. | ||
|keywords=Warburg effect | |keywords=Warburg effect, Pyruvate kinase, Triosephosphate isomerase, Reactive oxygen species | ||
|mipnetlab=AT Salzburg Breitenbach M | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
|area=Respiration | |||
|injuries=Oxidative stress;RONS | |||
|organism=Saccharomyces cerevisiae, Fungi | |||
|topics=Aerobic glycolysis, Redox state | |||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
}} | }} | ||
Latest revision as of 09:21, 9 November 2016
| Grüning NM, Rinnerthaler M, Bluemlein K, Mülleder M, Wamelink MM, Lehrach H, Jakobs C, Breitenbach M, Ralser M (2011) Pyruvate kinase triggers a metabolic feedback loop that controls redox metabolism in respiring cells. Cell Metab 14:415-27. |
Gruening NM, Rinnerthaler M, Bluemlein K, Muelleder M, Wamelink MM, Lehrach H, Jakobs C, Breitenbach M, Ralser M (2011) Cell Metab
Abstract: In proliferating cells, a transition from aerobic to anaerobic metabolism is known as the Warburg effect, whose reversal inhibits cancer cell proliferation. Studying its regulator pyruvate kinase (PYK) in yeast, we discovered that central metabolism is self-adapting to synchronize redox metabolism when respiration is activated. Low PYK activity activated yeast respiration. However, levels of reactive oxygen species (ROS) did not increase, and cells gained resistance to oxidants. This adaptation was attributable to accumulation of the PYK substrate phosphoenolpyruvate (PEP). PEP acted as feedback inhibitor of the glycolytic enzyme triosephosphate isomerase (TPI). TPI inhibition stimulated the pentose phosphate pathway, increased antioxidative metabolism, and prevented ROS accumulation. Thus, a metabolic feedback loop, initiated by PYK, mediated by its substrate and acting on TPI, stimulates redox metabolism in respiring cells. Originating from a single catalytic step, this autonomous reconfiguration of central carbon metabolism prevents oxidative stress upon shifts between fermentation and respiration. • Keywords: Warburg effect, Pyruvate kinase, Triosephosphate isomerase, Reactive oxygen species
• O2k-Network Lab: AT Salzburg Breitenbach M
Labels: MiParea: Respiration
Stress:Oxidative stress;RONS Organism: Saccharomyces cerevisiae, Fungi
Regulation: Aerobic glycolysis, Redox state
HRR: Oxygraph-2k
