Gregg 2019 J Biol Chem: Difference between revisions
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|keywords=Complex I, RO-3306, Calcium, Cyclin B1, Cyclin-dependent kinase 1 (CDK1), Insulin secretion, Mitochondrial metabolism, ob/ob mice, Obesity, Pancreatic beta cell | |keywords=Complex I, RO-3306, Calcium, Cyclin B1, Cyclin-dependent kinase 1 (CDK1), Insulin secretion, Mitochondrial metabolism, ob/ob mice, Obesity, Pancreatic beta cell | ||
|editor=[[Plangger M]], | |editor=[[Plangger M]], | ||
|mipnetlab=US WI Madison Denu JM | |||
}} | }} | ||
{{Labeling | {{Labeling | ||
|area=Respiration | |area=Respiration | ||
|diseases=Obesity | |||
|organism=Mouse | |||
|tissues=Islet cell;pancreas;thymus | |||
|preparations=Permeabilized tissue | |||
|couplingstates=OXPHOS, ET | |||
|pathways=N, S, NS, ROX | |||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|additional=Labels, 2019-02, | |additional=Labels, 2019-02, | ||
}} | }} |
Revision as of 16:39, 6 February 2019
Gregg T, Sdao SM, Dhillon RS, Rensvold JW, Lewandowski SL, Pagliarini DJ, Denu JM, Merrins MJ (2019) Obesity-dependent CDK1 signaling stimulates mitochondrial respiration at complex I in pancreatic ฮฒ-cells. J Biol Chem [Epub ahead of print]. |
Gregg T, Sdao SM, Dhillon RS, Rensvold JW, Lewandowski SL, Pagliarini DJ, Denu JM, Merrins MJ (2019) J Biol Chem
Abstract: ฮฒ-cell mitochondria play a central role in coupling glucose metabolism with insulin secretion. Here, we identified a metabolic function of cyclin-dependent kinase 1 (CDK1)/cyclin B1 - the activation of mitochondrial respiratory complex I - that is active in quiescent adult ฮฒ-cells and hyperactive in ฮฒ-cells from obese (ob/ob) mice. In wild-type islets, respirometry revealed that 65% of complex I flux and 49% of state 3 respiration is sensitive to CDK1 inhibition. Islets from ob/ob mice expressed more cyclin B1 and exhibited a higher sensitivity to CDK1 blockade, which reduced complex I flux by 76% and state 3 respiration by 79%. The ensuing reduction in mitochondrial NADH utilization, measured with 2-photon NAD(P)H fluorescence lifetime imaging (FLIM), was matched in the cytosol by a lag in citrate cycling, as shown with a FRET reporter targeted to ฮฒ-cells. Moreover, time-resolved measurements revealed that in ob/ob islets, where complex I flux dominates respiration, CDK1 inhibition is sufficient to restrict the duty cycle of ATP/ADP and calcium oscillations, the parameter that dynamically encodes ฮฒ-cell glucose sensing. Direct complex I inhibition with rotenone mimicked the restrictive effects of CDK1 inhibition on mitochondrial respiration, NADH turnover, ATP/ADP, and calcium influx. These findings identify complex I as a critical mediator of obesity-associated metabolic remodeling in ฮฒ-cells, and implicate CDK1 as a regulator of complex I that enhances ฮฒ-cell glucose sensing.
Published under license by The American Society for Biochemistry and Molecular Biology, Inc. โข Keywords: Complex I, RO-3306, Calcium, Cyclin B1, Cyclin-dependent kinase 1 (CDK1), Insulin secretion, Mitochondrial metabolism, ob/ob mice, Obesity, Pancreatic beta cell โข Bioblast editor: Plangger M โข O2k-Network Lab: US WI Madison Denu JM
Labels: MiParea: Respiration
Pathology: Obesity
Organism: Mouse Tissue;cell: Islet cell;pancreas;thymus Preparation: Permeabilized tissue
Coupling state: OXPHOS, ET
Pathway: N, S, NS, ROX
HRR: Oxygraph-2k
Labels, 2019-02