The energy supplies of modern society seem to be necessarily associated with risks. In this paper, we address the question as to whether the efficient utilisation of energy in biological systems is also coupled to hazards. Most organisms oxidise highly reduced substrates with molecular oxygen in order to gain energy. In eukaryotes, this process takes place at the inner membrane of specialised organelles, the mitochondria. Interestingly, about 1% of the consumed oxygen molecules are reduced not to water, but to ROS (reactive oxygen species), which are deleterious to many macromolecules, including mitochondrial DNA. As a result, mitochondrial DNA mutations accumulate, in turn affecting the energy supply and inducing degeneration and ageing. / Nach dem heutigen Stand der Technik scheint eine ausreichende Energieversorgung der Gesellschaft stets mit Risiken verbunden zu sein. Wir gehen in dem Artikel der Frage nach, ob auch biologische Systeme bei der Nutzung von Energie Risiken in Kauf nehmen. Zur effizienten Energiegewinnung nutzen Organismen meist Sauerstoff zur Oxidation energiereicher Substrate. In Eukaryonten erfolgt die Energiegewinnung vor allem an der inneren Membran von Mitochondrien. Etwa 1 % des verbrauchten Sauerstoffs wird dabei nicht zu Wasser, sondern zu ROS (reactive oxygen species, reaktive Sauerstoffspezies) reduziert, die unter anderem die mitochondriale DNA schädigen und Mutationen hervorrufen. Diese akkumulieren auf Dauer und führen zu einer Störung der Energiegewinnung, in deren Folge Degenerations- und Alterungsphänomene auftreten.

Thesis (Ph. D.)--Ohio State University, 2007. / Title from first page of PDF file. Includes bibliographical references (p. 128-141).

Thesis (Ph. D.)--Illinois State University, 1974. / Title from title page screen, viewed Oct. 28, 2004. Dissertation Committee: H.E. Brockman, A.G. Richardson (co-chairs), A.E. Liberta, H.W. Huizinga, D. McCracken, F. Schwalm. Includes bibliographical references (leaves 119-140) and abstract. Also available in print.

No description available.

A velocidade específica de respiração (QO2) é um parâmetro fundamental para entender-se o metabolismo e o estado fisiológico celular, fornecendo informações úteis para o processo e controle em biorreatores. Neste trabalho, cultivou-se diferentes células de insetos em ambiente controlado medindo-se o QO2 e concentração crítica de oxigênio (Ccrít). Foram utilizadas nos ensaios células de insetos Spodoptera frugiperda (Sf9) não infectadas e células de Drosophila melanogaster (S2) selvagem e recombinantes, utilizadas na expressão de diferentes proteínas. Todas as experiências foram realizadas em biorreator Inceltech com volume de trabalho de 1L, mantido a temperatura de 28ºC, agitação de 100 rpm e oxigênio dissolvido (OD) a 40% da saturação de ar, com difusão por membrana de silicone com mistura gasosa (O2 e N2) e vazão gasosa constante. Foi utilizado meio de cultura Sf900II sem soro fetal bovino. O QO2 foi medido pelo método dinâmico e pelo balanço de oxigênio na fase líquida. Neste trabalho foi implementado um novo processo durante o método dinâmico para interromper completamente a transferência gasosa durante a execução deste método. Implementou-se também uma metodologia para medição de Ccrít. Chegou-se a concentrações máximas celulares (Xm), velocidades máximas específicas de respiração (QO2) na fase exponencial e Ccrít, conforme segue: 1) Sf9 (ATCC 1711): Xm - 10,7.106 cel/mL; QO2 - 74,7.10-18 molO2/(cel.s); 2) S2 (Invitrogen): Xm - 51,2.106 cel/mL; QO2 - 3,4.10-18 molO2/(cel.s); Ccrít - 10%; 3) S2AcGPV2 (transfectadas para expressão de GPV): Xm - 26,6.106 cel/mL; QO2 -16,0.10-18 molO2/(cel.s); Ccrít - 10%; 4) S2MtEGFP (transfectadas para expressão de EGFP): Xm - 17,8.106 cel/mL; QO2 - 25,8.10-18 molO2/(cel.s); Ccrít - 5%; 5) S2AcHBsAgHy (transfectadas para expressão de HBsAg): Xm - 16,6.106 cel/mL; QO2 -33,6.10-18 molO2/(cel.s); Ccrít - 12%. Conclui-se que as linhagens selvagens e transfectadas de S2 possuem entre si uma atividade respiratória diferente e também que as novas metodologias implantadas verificaram-se satisfatoriamente. / Specific respiration rate (QO2) is a key parameter to understand cell metabolism and physiological state, providing useful information for process supervision and control. In this work, we cultivated different insect cells in a very controlled environment, being able to measure QO2 and critical oxygen concentration (Ccrit). Wild Spodoptera frugiperda (Sf9) and wild and transfected Drosophila melanogaster S2 cells (able to produce different proteins) were used. All experiments were performed in 1-liter working volume Inceltech bioreactor, maintaining temperature controlled at 28ºC, agitation rate at 100 rpm, and dissolved oxygen (DO) at 40% of air saturation, through membrane diffusion of mixed gases (O2 and N2) at constant total flow rate. SF900II serum free medium was used. QO2 was measured through dynamic method and oxygen mass balance in the liquid phase. In this work a new process was implemented during the dynamic method to interrupt completely the oxygen transfer during the execution of this method. It was also implemented a methodology for measurement of Ccrít (determined when DO reduces its decay rate, without oxygen transfer). Maximum cell concentration (Xm), maximum specific respiration rate (QO2) in the exponential phase and Ccrít were reached, as follows: 1) Sf9 (ATCC 1711): Xm - 10,7.106 cel/mL; QO2 - 74,7.10-18 molO2/(cel.s); 2) S2 (Invitrogen): Xm - 51,2.106 cel/mL; QO2 - 3,4.10-18 molO2/(cel.s); Ccrít - 10%; 3) S2AcGPV2 (transfected for GPV expression): Xm - 26,6.106 cel/mL; QO2 -16,0.10-18 molO2/(cel.s); Ccrít - 10%; 4) S2MtEGFP (transfected for EGFP expression): Xm - 17,8.106 cel/mL; QO2 - 25,8.10-18 molO2/(cel.s); Ccrít - 5%; 5) S2AcHBsAgHy (transfected for HbsAg expression): Xm - 16,6.106 cel/mL; QO2 -33,6.10-18 molO2/(cel.s); Ccrít - 12%. From these results, it can be concluded that the studied cell lines have different respiration activity and the new developed methodologies behave satisfactorily.

A velocidade específica de respiração (QO2) é um parâmetro fundamental para entender-se o metabolismo e o estado fisiológico celular, fornecendo informações úteis para o processo e controle em biorreatores. Neste trabalho, cultivou-se diferentes células de insetos em ambiente controlado medindo-se o QO2 e concentração crítica de oxigênio (Ccrít). Foram utilizadas nos ensaios células de insetos Spodoptera frugiperda (Sf9) não infectadas e células de Drosophila melanogaster (S2) selvagem e recombinantes, utilizadas na expressão de diferentes proteínas. Todas as experiências foram realizadas em biorreator Inceltech com volume de trabalho de 1L, mantido a temperatura de 28ºC, agitação de 100 rpm e oxigênio dissolvido (OD) a 40% da saturação de ar, com difusão por membrana de silicone com mistura gasosa (O2 e N2) e vazão gasosa constante. Foi utilizado meio de cultura Sf900II sem soro fetal bovino. O QO2 foi medido pelo método dinâmico e pelo balanço de oxigênio na fase líquida. Neste trabalho foi implementado um novo processo durante o método dinâmico para interromper completamente a transferência gasosa durante a execução deste método. Implementou-se também uma metodologia para medição de Ccrít. Chegou-se a concentrações máximas celulares (Xm), velocidades máximas específicas de respiração (QO2) na fase exponencial e Ccrít, conforme segue: 1) Sf9 (ATCC 1711): Xm - 10,7.106 cel/mL; QO2 - 74,7.10-18 molO2/(cel.s); 2) S2 (Invitrogen): Xm - 51,2.106 cel/mL; QO2 - 3,4.10-18 molO2/(cel.s); Ccrít - 10%; 3) S2AcGPV2 (transfectadas para expressão de GPV): Xm - 26,6.106 cel/mL; QO2 -16,0.10-18 molO2/(cel.s); Ccrít - 10%; 4) S2MtEGFP (transfectadas para expressão de EGFP): Xm - 17,8.106 cel/mL; QO2 - 25,8.10-18 molO2/(cel.s); Ccrít - 5%; 5) S2AcHBsAgHy (transfectadas para expressão de HBsAg): Xm - 16,6.106 cel/mL; QO2 -33,6.10-18 molO2/(cel.s); Ccrít - 12%. Conclui-se que as linhagens selvagens e transfectadas de S2 possuem entre si uma atividade respiratória diferente e também que as novas metodologias implantadas verificaram-se satisfatoriamente. / Specific respiration rate (QO2) is a key parameter to understand cell metabolism and physiological state, providing useful information for process supervision and control. In this work, we cultivated different insect cells in a very controlled environment, being able to measure QO2 and critical oxygen concentration (Ccrit). Wild Spodoptera frugiperda (Sf9) and wild and transfected Drosophila melanogaster S2 cells (able to produce different proteins) were used. All experiments were performed in 1-liter working volume Inceltech bioreactor, maintaining temperature controlled at 28ºC, agitation rate at 100 rpm, and dissolved oxygen (DO) at 40% of air saturation, through membrane diffusion of mixed gases (O2 and N2) at constant total flow rate. SF900II serum free medium was used. QO2 was measured through dynamic method and oxygen mass balance in the liquid phase. In this work a new process was implemented during the dynamic method to interrupt completely the oxygen transfer during the execution of this method. It was also implemented a methodology for measurement of Ccrít (determined when DO reduces its decay rate, without oxygen transfer). Maximum cell concentration (Xm), maximum specific respiration rate (QO2) in the exponential phase and Ccrít were reached, as follows: 1) Sf9 (ATCC 1711): Xm - 10,7.106 cel/mL; QO2 - 74,7.10-18 molO2/(cel.s); 2) S2 (Invitrogen): Xm - 51,2.106 cel/mL; QO2 - 3,4.10-18 molO2/(cel.s); Ccrít - 10%; 3) S2AcGPV2 (transfected for GPV expression): Xm - 26,6.106 cel/mL; QO2 -16,0.10-18 molO2/(cel.s); Ccrít - 10%; 4) S2MtEGFP (transfected for EGFP expression): Xm - 17,8.106 cel/mL; QO2 - 25,8.10-18 molO2/(cel.s); Ccrít - 5%; 5) S2AcHBsAgHy (transfected for HbsAg expression): Xm - 16,6.106 cel/mL; QO2 -33,6.10-18 molO2/(cel.s); Ccrít - 12%. From these results, it can be concluded that the studied cell lines have different respiration activity and the new developed methodologies behave satisfactorily.

Mitochondria are multifunctional organelles playing a key role in energy metabolism and cell death induction. Mitochondria, and specifically their respiratory chain, are also the main producers of reactive oxygen species (ROS) in cells. Metabolism can be affected by the state of cellular proliferation and certain ROS-inducing agents have an antiangiogenic effect based on the preferential elimination of proliferating endothelial cells (EC). Therefore, in this work we investigated, whether mitochondria could be responsible for different sensitivity of proliferation and confluent EC to cell death. We mainly focused on systems that regulate ROS level and apoptosis: respiratory chain (ROS production), antioxidant defense (ROS detoxification) and Bcl-2 family of proteins (apoptosis regulation). First, we treated EC with functional and nonfunctional respiratory chain with various oxidative stress- and apoptosis-inducing agents and determined ROS production and susceptibility to apoptosis in proliferating and confluent cells. Our results show that functional respiratory chain greatly increases the susceptibility of proliferating cells to ROS induction and apoptosis, whereas in qiescent cells it protects against cell death. Given these findings, we assessed the activity of respiratory chain in proliferating...

The energy supplies of modern society seem to be necessarily associated with risks. In this paper, we address the question as to whether the efficient utilisation of energy in biological systems is also coupled to hazards. Most organisms oxidise highly reduced substrates with molecular oxygen in order to gain energy. In eukaryotes, this process takes place at the inner membrane of specialised organelles, the mitochondria. Interestingly, about 1% of the consumed oxygen molecules are reduced not to water, but to ROS (reactive oxygen species), which are deleterious to many macromolecules, including mitochondrial DNA. As a result, mitochondrial DNA mutations accumulate, in turn affecting the energy supply and inducing degeneration and ageing. / Nach dem heutigen Stand der Technik scheint eine ausreichende Energieversorgung der Gesellschaft stets mit Risiken verbunden zu sein. Wir gehen in dem Artikel der Frage nach, ob auch biologische Systeme bei der Nutzung von Energie Risiken in Kauf nehmen. Zur effizienten Energiegewinnung nutzen Organismen meist Sauerstoff zur Oxidation energiereicher Substrate. In Eukaryonten erfolgt die Energiegewinnung vor allem an der inneren Membran von Mitochondrien. Etwa 1 % des verbrauchten Sauerstoffs wird dabei nicht zu Wasser, sondern zu ROS (reactive oxygen species, reaktive Sauerstoffspezies) reduziert, die unter anderem die mitochondriale DNA schädigen und Mutationen hervorrufen. Diese akkumulieren auf Dauer und führen zu einer Störung der Energiegewinnung, in deren Folge Degenerations- und Alterungsphänomene auftreten.

Oxidative stress represents a complex and intensely studied phenomenon tightly linked to a range of human diseases, and to aging in many organisms. A plethora of key cellular regulators, including the Notch signaling pathway, have been recently described to respond to the cellular redox status. We have characterized the role of CSL (CBF1/Su(H)/LAG-1) proteins, the effectors of Notch signaling pathway in metazoa, in oxidative stress response in fission yeast. Schizosaccharomyces pombe contains two CSL paralogs, Cbf11 and Cbf12, that have antagonistic functions in the regulation of cell cycle and cellular adhesion. Both proteins are able to bind the canonical CSL motif and activate transcription and, thus, function as genuine CSL transcription factors. We have determined that the strain lacking cbf11 is resistant to hydrogen peroxide but not to menadione, a source of superoxide anion radical. Using double knock-outs to assess genetic interactions we have revealed that the resistance of cbf11 knock-out is dependent on the antioxidants catalase and sulfiredoxin. Genes encoding these antioxidants are under transcriptional control of the Sty1 MAP kinase pathway and the Pap1 transcription factor which are also required for the resistance of Δcbf11 cells. Cbf12 is believed to play only a minor role in...

Abstract Heart muscle has to work constantly throughout the life and its energy metabolism is heavily dependent on a continuous supply of oxygen. Energy metabolism must be effectively regulated to meet the demands of changing workloads in different circumstances. If the oxygen supply is interrupted, the function of the heart is easily disturbed and cells injured. Calcium metabolism is of great importance in these pathological conditions. In this thesis respiratory regulation was studied by non-destructive optical methods in mouse heart. The myoglobin-deficient mouse was used as an experimental model to avoid the artefact caused by intracellular myoglobin. Results show that increased consumption of energy and oxygen lead to concomitant reduction of cytochrome aa3 and oxidation of flavoproteins. This finding supports the view that cell respiration in intact myocardium is dominantly regulated at the level of the respiratory chain. The intracellular Ca2+ accumulation during ischemia is one of the major causes of irreversible ischemia-reperfusion injury. Ischemic preconditioning (IPC) has been shown to protect the heart muscle significantly from ischemic damage. In this thesis Ca2+ accumulation during ischemia and reperfusion was studied in perfused rat heart using Fura-2 as a fluorescent Ca2+ indicator. As there is a significant decrease in intracellular pH during prolonged ischemia, the pH-dependency of Fura-2 signal was taken into account. It was found that IPC attenuates Ca2+accumulation during ischemia and this was connected to a decrease in mitochondrial membrane potential. Both IPC and the pharmacologically induced preconditioning with the mitoKATP opener diaxozide were shown to be associated with increased production of superoxide monitored by means of lucigenin chemiluminescence. The superoxide production correlated with the oxidation-reduction state of flavoproteins. We also describe here a method for measuring of intracellular free Ca2+ in mouse heart during ischemia by simultaneous monitoring of Fura-2 and the pH probe BCECF fluorescence by means of dual wavelength excitation of both probes. The paradoxical decrease of Fura-2 fluorescence during ischemia indicating decreasing intracellular Ca2+ concentration was due to the pH effect on the dissociation constant of the Fura-2-Ca2+ complex. When the pH-dependency of Fura-2 was compensated, an extensive Ca2+ accumulation during ischemia was detected. Much of the previous literature on this subject must be re-evaluated because the pH-dependency of intracellular Ca2+ probes has been largely overlooked.