RESUMO
BACKGROUND: The catalytic subunit of telomerase, telomerase reverse transcriptase (TERT), has protective functions in the cardiovascular system. TERT is not only present in the nucleus but also in mitochondria. However, it is unclear whether nuclear or mitochondrial TERT is responsible for the observed protection, and the appropriate tools are missing to dissect this. METHODS: We generated new mouse models containing TERT exclusively in the mitochondria (mitoTERT mice) or the nucleus (nucTERT mice) to finally distinguish between the functions of nuclear and mitochondrial TERT. Outcome after ischemia/reperfusion, mitochondrial respiration in the heart, and cellular functions of cardiomyocytes, fibroblasts, and endothelial cells, as well, were determined. RESULTS: All mice were phenotypically normal. Although respiration was reduced in cardiac mitochondria from TERT-deficient and nucTERT mice, it was increased in mitoTERT animals. The latter also had smaller infarcts than wild-type mice, whereas nucTERT animals had larger infarcts. The decrease in ejection fraction after 1, 2, and 4 weeks of reperfusion was attenuated in mitoTERT mice. Scar size was also reduced and vascularization increased. Mitochondrial TERT protected a cardiomyocyte cell line from apoptosis. Myofibroblast differentiation, which depends on complex I activity, was abrogated in TERT-deficient and nucTERT cardiac fibroblasts and completely restored in mitoTERT cells. In endothelial cells, mitochondrial TERT enhanced migratory capacity and activation of endothelial nitric oxide synthase. Mechanistically, mitochondrial TERT improved the ratio between complex I matrix arm and membrane subunits, explaining the enhanced complex I activity. In human right atrial appendages, TERT was localized in mitochondria and there increased by remote ischemic preconditioning. The telomerase activator TA-65 evoked a similar effect in endothelial cells, thereby increasing their migratory capacity, and enhanced myofibroblast differentiation. CONCLUSIONS: Mitochondrial, but not nuclear TERT, is critical for mitochondrial respiration and during ischemia/reperfusion injury. Mitochondrial TERT improves complex I subunit composition. TERT is present in human heart mitochondria, and remote ischemic preconditioning increases its level in those organelles. TA-65 has comparable effects ex vivo and improves the migratory capacity of endothelial cells and myofibroblast differentiation. We conclude that mitochondrial TERT is responsible for cardioprotection, and its increase could serve as a therapeutic strategy.
Assuntos
Complexo I de Transporte de Elétrons/metabolismo , Mitocôndrias Cardíacas/enzimologia , Proteínas Mitocondriais/metabolismo , Traumatismo por Reperfusão Miocárdica/enzimologia , Telomerase/metabolismo , Animais , Complexo I de Transporte de Elétrons/genética , Feminino , Humanos , Masculino , Camundongos , Camundongos Transgênicos , Mitocôndrias Cardíacas/genética , Proteínas Mitocondriais/genética , Traumatismo por Reperfusão Miocárdica/genética , Telomerase/genéticaRESUMO
Global climate and the concentration of atmospheric carbon dioxide (CO2) are correlated over recent glacial cycles. The combination of processes responsible for a rise in atmospheric CO2 at the last glacial termination (23,000 to 9,000 years ago), however, remains uncertain. Establishing the timing and rate of CO2 changes in the past provides critical insight into the mechanisms that influence the carbon cycle and helps put present and future anthropogenic emissions in context. Here we present CO2 and methane (CH4) records of the last deglaciation from a new high-accumulation West Antarctic ice core with unprecedented temporal resolution and precise chronology. We show that although low-frequency CO2 variations parallel changes in Antarctic temperature, abrupt CO2 changes occur that have a clear relationship with abrupt climate changes in the Northern Hemisphere. A significant proportion of the direct radiative forcing associated with the rise in atmospheric CO2 occurred in three sudden steps, each of 10 to 15 parts per million. Every step took place in less than two centuries and was followed by no notable change in atmospheric CO2 for about 1,000 to 1,500 years. Slow, millennial-scale ventilation of Southern Ocean CO2-rich, deep-ocean water masses is thought to have been fundamental to the rise in atmospheric CO2 associated with the glacial termination, given the strong covariance of CO2 levels and Antarctic temperatures. Our data establish a contribution from an abrupt, centennial-scale mode of CO2 variability that is not directly related to Antarctic temperature. We suggest that processes operating on centennial timescales, probably involving the Atlantic meridional overturning circulation, seem to be influencing global carbon-cycle dynamics and are at present not widely considered in Earth system models.
Assuntos
Ciclo do Carbono , Regiões Antárticas , Atmosfera/química , Dióxido de Carbono/análise , Efeito Estufa , Groenlândia , História Antiga , Camada de Gelo , Isótopos , Metano/análise , Oceanos e Mares , Água/análise , Água/químicaAssuntos
Conservação dos Recursos Naturais/métodos , Conservação dos Recursos Naturais/tendências , Ecossistema , Aquecimento Global/estatística & dados numéricos , Camada de Gelo , Animais , Regiões Árticas , Canadá , Aquecimento Global/prevenção & controle , Groenlândia , Plâncton/metabolismo , Estações do Ano , Ursidae , MorsasAssuntos
Modelos Teóricos , Preconceito/prevenção & controle , Projetos de Pesquisa/normas , Pesquisadores/psicologia , Animais , Teorema de Bayes , Interpretação Estatística de Dados , Feminino , Previsões , Masculino , Preconceito/psicologia , Reprodutibilidade dos Testes , Projetos de Pesquisa/tendênciasRESUMO
Fearing supply disruptions, industry calls for delay to unloading of federal reserve.
RESUMO
Telomerase consists of the catalytic subunit Telomerase Reverse Transcriptase (TERT) and the Telomerase RNA Component. Its canonical function is the prevention of telomere erosion. Over the last years it became evident that TERT is also present in tissues with low replicative potential. Important non-canonical functions of TERT are protection against apoptosis and maintenance of the cellular redox homeostasis in cancer as well as in somatic tissues. Intriguingly, TERT and reactive oxygen species (ROS) are interdependent on each other, with TERT being regulated by changes in the redox balance and itself controlling ROS levels in the cytosol and in the mitochondria. The latter is achieved because TERT is present in the mitochondria, where it protects mitochondrial DNA and maintains levels of anti-oxidative enzymes. Since numerous diseases are associated with oxidative stress, increasing the mitochondrial TERT level could be of therapeutic value.
Assuntos
Telomerase , Homeostase , Mitocôndrias/genética , Mitocôndrias/metabolismo , Oxirredução , Telomerase/genética , Telomerase/metabolismo , Telômero/genética , Telômero/metabolismoRESUMO
Nutritional and metabolic exposure during critical periods of early human development can have a long-term programming effect on health in adulthood. This is supported by evidence from epidemiological studies, numerous animal models and clinical intervention trials. An improved understanding of the mechanisms and effects of metabolic programming has the potential to contribute significantly to the prevention of some major health risks. Obesity and the metabolic syndrome, whose prevalences increase in almost all countries of the world, may have partly developmental origins. Collaboration of clinicians, epidemiologists and basic scientists in an EU funded research project on the relationship between early nutrition and later health (The EU Early Nutrition Programming Project, www.metabolic-programming.org) should provide further insights into metabolic programming and help to transfer scientific progress into clinical practice.