scholarly journals PGC1α and Exercise Adaptations in Zebrafish

2018 ◽  
Author(s):  
Alice Parisi ◽  
Peter Blattmann ◽  
Giulia Lizzo ◽  
Vivienne Stutz ◽  
Laura Strohm ◽  
...  

ABSTRACTFish species display huge differences in physical activity ranging from lethargy to migration of thousands of miles, making them an interesting model to identify determinants of physical fitness. Here, we show a remarkable plasticity of zebrafish in response to exercise and induction of PGC1α (encoded by PPARGC1A), a dominant regulator of mitochondrial biogenesis. Forced expression of human PPARGC1A induces mitochondrial biogenesis, an exercise-like gene expression signature, and physical fitness comparable to wild-type animals trained in counter-current swim tunnels. Quantifying transcriptional and proteomic changes in response to exercise or PGC1α, we identify conserved ‘exercise’ adaptations, including a stoichiometric induction of the electron transport chain (ETC) that re-organizes into respiratory supercomplexes in both conditions. We further show that ndufa4/ndufa4l, previously assigned to complex I, associates to free and supramolecular complex IV in vivo. Thus, zebrafish is a useful and experimentally tractable vertebrate model to study exercise biology, including ETC expression and assembly.HIGHLIGHTSPGC1α reprograms zebrafish skeletal muscle to a ‘red fiber’ phenotype and increases exercise performanceZebrafish show a high molecular plasticity in response to PGC1α and exerciseSWATH-MS proteomics show a stoichiometric induction of the electron transport chain that organizes as supercomplexes in response to PGC1α and exercisendufa4/ndufa4l associate to free and supramolecular complex IV in vivo

2021 ◽  
Author(s):  
Jong Hyun Kim ◽  
Samuel Ofori ◽  
Sean Parkin ◽  
Hemendra Vekaria ◽  
Patrick G. Sullivan ◽  
...  

Expanding the chemical diversity of metal complexes provides a robust platform to generate functional bioactive reagents.


1976 ◽  
Vol 3 (6) ◽  
pp. 771
Author(s):  
K.C Woo ◽  
C.B Osmond

Mitochondria isolated from spinach leaves contain at least two glycine decarboxylating systems. One system is stimulated by ADP and evidently couples to the electron transport chain. The other system, three times as active, is stimulated by NAD+ and oxaloacetate and is not coupled directly to electron transport; however, comparative studies with uncouplers and inhibitors indicate it may depend on a membrane potential generated by electron transport. In this system, the role of oxaloacetate appears to be the regeneration of NAD+, via mitochondrial malate dehydrogenase, as an electron acceptor during glycine decarboxylation. Mitochondria isolated from spinach leaves also catalyse a rapid glycine-dependent exchange of bicarbonate into acid-stable products. This reaction is stimulated by the addition of lipoamide dehydrogenase. The activity of the glycine decarboxylation and exchange reactions are irreversibly lost when mitochondria are broken. When corrections are applied to account for mitochondrial breakage, the rates of glycine decarboxylation and the exchange reaction are comparable to the rates of CO*2 evolution from leaves of C*3 plants in air. The role of these processes in vivo and relationship to other sources of CO*2 in the glycollate pathway are discussed.


2011 ◽  
Vol 22 (13) ◽  
pp. 2235-2245 ◽  
Author(s):  
Zhongyan Zhang ◽  
Nobunao Wakabayashi ◽  
Junko Wakabayashi ◽  
Yasushi Tamura ◽  
Woo-Jin Song ◽  
...  

Previous studies using in vitro cell culture systems have shown the role of the dynamin-related GTPase Opa1 in apoptosis prevention and mitochondrial DNA (mtDNA) maintenance. However, it remains to be tested whether these functions of Opa1 are physiologically important in vivo in mammals. Here, using the Cre-loxP system, we deleted mouse Opa1 in pancreatic beta cells, in which glucose-stimulated ATP production in mitochondria plays a key role in insulin secretion. Beta cells lacking Opa1 maintained normal copy numbers of mtDNA; however, the amount and activity of electron transport chain complex IV were significantly decreased, leading to impaired glucose-stimulated ATP production and insulin secretion. In addition, in Opa1-null beta cells, cell proliferation was impaired, whereas apoptosis was not promoted. Consequently, mice lacking Opa1 in beta cells develop hyperglycemia. The data suggest that the function of Opa1 in the maintenance of the electron transport chain is physiologically relevant in beta cells.


PLoS ONE ◽  
2010 ◽  
Vol 5 (9) ◽  
pp. e12733 ◽  
Author(s):  
Amy V. Pointon ◽  
Tracy M. Walker ◽  
Kate M. Phillips ◽  
Jinli Luo ◽  
Joan Riley ◽  
...  

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