850 research outputs found

    The Baleares 2013 Calibration Campaign of Jason-2 and Saral Altimeters

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    The 2013 Balearic campaign GNSS position analysis of the 2013 will be performed with different softwares by different groups (similarly as it is being done in the International GNSS Service for their different products), in order improve the high demanded accuracy for JASON2 and SARAL altimeters precise calibration. In particular JPL GIPSY-OASIS software will be used, with the undifferenced PPP ambiguity fixing strategy. In order to improve the results accuracy, two similar networks are being processed. The first network includes the deployed GNSS receivers and the reference stations. The second one is a control network, defined by using the permanent receivers in the California dense network with a similar distribution as the main altimeter campaign network. In this case, the position of the receivers plying the role of buoys are being processed in the same kinematic way than the actual buoys, in order to compare them with the very accurate positions obtained with GIPSY-OASIS static processing.Postprint (published version

    Inventory of Geological Sites of Interest in the Canary Islands

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    En el marco de proyecto de investigación LIGCANARIAS (2018-2021) se ha realizado el Inventario de Lugares de Interés Geológico de las Islas Canarias, que forma parte del Inventario Español de Lugares de Interés Geológico (IELIG) para el dominio de este archipiélago. El inventario ha empleado la metodología del IELIG adaptada a un dominio geológico eminentemente volcánico, partiendo de los contextos geológicos regionales. Consta de 300 LIG: 53 en Gran Canaria, 47 en Tenerife, 54 en Lanzarote y Archipiélago Chinijo, 40 en Fuerteventura, 29 en La Palma, 23 en La Gomera y 21 en El Hierro. La principal novedad con respecto a los inventarios en otros dominios geológicos es la identificación de 33 LIG submarinos.Within the framework of the LIGCANARIAS research project (2018-2021), the Inventory of Geological Sites of Interest of the Canary Islands has been carried out, which is part of the Spanish Inventory of Places of Geological Interest (IELIG) for the domain of this archipelago. The inventory has used the IELIG methodology adapted to an eminently volcanic geological domain, based on regional geological frameworks. It consists of 300 geosites: 53 in Gran Canaria, 47 in Tenerife, 54 in Lanzarote and Chinijo Archipelago, 40 in Fuerteventura, 29 in La Palma, 23 in La Gomera and 21 in El Hierro. The main novelty with respect to the inventories in other geological domains is the identification of 33 submarine geosites.Depto. de Mineralogía y PetrologíaFac. de Ciencias GeológicasTRUEAgencia Canaria de Investigación, Innovación y Sociedad de la Informaciónpu

    Enhanced mitochondrial activity reshapes a gut microbiota profile that delays NASH progression

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    [EN] Background and Aims: Recent studies suggest that mitochondrial dysfunction promotes progression to NASH by aggravating the gut-liver status. However, the underlying mechanism remains unclear. Herein, we hypothesized that enhanced mitochondrial activity might reshape a specific microbiota signature that, when transferred to germ-free (GF) mice, could delay NASH progression. Approach and Results: Wild-type and methylation-controlled J protein knockout (MCJ-KO) mice were fed for 6 weeks with either control or a choline-deficient, L-amino acid–defined, high-fat diet (CDA-HFD). One mouse of each group acted as a donor of cecal microbiota to GF mice, who also underwent the CDA-HFD model for 3 weeks. Hepatic injury, intestinal barrier, gut microbiome, and the associated fecal metabolome were then studied. Following 6 weeks of CDA-HFD, the absence of methylation-controlled J protein, an inhibitor of mitochondrial complex I activity, reduced hepatic injury and improved gut-liver axis in an aggressive NASH dietary model. This effect was transferred to GF mice through cecal microbiota transplantation. We suggest that the specific microbiota profile of MCJ-KO, characterized by an increase in the fecal relative abundance of Dorea and Oscillospira genera and a reduction in AF12, Allboaculum, and [Ruminococcus], exerted protective actions through enhancing short-chain fatty acids, nicotinamide adenine dinucleotide (NAD+) metabolism, and sirtuin activity, subsequently increasing fatty acid oxidation in GF mice. Importantly, we identified Dorea genus as one of the main modulators of this microbiota-dependent protective phenotype. Conclusions: Overall, we provide evidence for the relevance of mitochondria–microbiota interplay during NASH and that targeting it could be a valuable therapeutic approach.S

    Near barrier scattering of 8He on 208Pb

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    The exotic nucleus 8He is investigated by means of the measurement of the angular distributions of the elastic channel and the 6He and 4He fragment yields produced in the collision with a 208Pb target at two energies around the Coulomb barrier, 16 and 22 MeV. The experiment was performed at the GANIL-SPIRAL facility, with the aim of extracting information about the structure of 8He and the relevant reaction mechanisms. In this contribution, details of the experimental setup and preliminary data on elastic cross sections are reporte

    Mitochondrial bioenergetics boost macrophage activation, promoting liver regeneration in metabolically compromised animals

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    Background and aims: Hepatic ischemia-reperfusion injury (IRI) is the leading cause of early posttransplantation organ failure as mitochondrial respiration and ATP production are affected. A shortage of donors has extended liver donor criteria, including aged or steatotic livers, which are more susceptible to IRI. Given the lack of an effective treatment and the extensive transplantation waitlist, we aimed at characterizing the effects of an accelerated mitochondrial activity by silencing methylation-controlled J protein (MCJ) in three preclinical models of IRI and liver regeneration, focusing on metabolically compromised animal models. Approach and results: Wild-type (WT), MCJ knockout (KO), and Mcj silenced WT mice were subjected to 70% partial hepatectomy (Phx), prolonged IRI, and 70% Phx with IRI. Old and young mice with metabolic syndrome were also subjected to these procedures. Expression of MCJ, an endogenous negative regulator of mitochondrial respiration, increases in preclinical models of Phx with or without vascular occlusion and in donor livers. Mice lacking MCJ initiate liver regeneration 12 h faster than WT and show reduced ischemic injury and increased survival. MCJ knockdown enables a mitochondrial adaptation that restores the bioenergetic supply for enhanced regeneration and prevents cell death after IRI. Mechanistically, increased ATP secretion facilitates the early activation of Kupffer cells and production of TNF, IL-6, and heparin-binding EGF, accelerating the priming phase and the progression through G1 /S transition during liver regeneration. Therapeutic silencing of MCJ in 15-month-old mice and in mice fed a high-fat/high-fructose diet for 12 weeks improves mitochondrial respiration, reduces steatosis, and overcomes regenerative limitations. Conclusions: Boosting mitochondrial activity by silencing MCJ could pave the way for a protective approach after major liver resection or IRI, especially in metabolically compromised, IRI-susceptible organs.Funding information: Supported by grants from Ministerio de Ciencia, Innovación y Universidades MICINN (PID2020-117116RB-100, RTI2018-096759-A-100, RTI2018-095114-B-I00, PID2019-108977RB-100 and RTI2018-095700-B100, integrado en el Plan Estatal de Investigación Científica y Técnica y Innovación, cofinanciado con Fondos FEDER, to M.L.M.-C., T.C.D., C.P., P.M.-S., and N.G.A.A., respectively), Subprograma Retos Colaboración RTC2019-007125-1; Fundación Científica de la Asociación Española Contra el Cáncer (AECC Scientific Foundation) Rare Tumor Calls 2017 (to M.L.M.-C.); Asociación Española contra el Cáncer (to T.C.D. and M.S.-M); La Caixa Foundation Program (HR17-00601, to M.L.M.-C.), Proyectos Investigación en Salud DTS20/00138 (to M.L.M.-C.); Departamento de Industria del Gobierno Vasco (to M.L.M.-C.); Departamento de Educación del Gobierno Vasco (to N.G.-U. and J.S.); Acción Estratégica Ciber Emergentes 2018 (Ciberehd-ISCIII) and Gilead Sciences International Research Scholars Program in Liver Disease (to M.V.-R.); Ciberehd_ISCIII_MINECO is funded by the Instituto de Salud Carlos IIIAcknowledgments: We thank MINECO for the Severo Ochoa Excellence Accreditation to CIC bioGUNE (SEV-2016-0644). We acknowledge Begoña Rodríguez Iruretagoyena for the technical support provided

    p38γ is essential for cell cycle progression and liver tumorigenesis

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    The cell cycle is a tightly regulated process that is controlled by the conserved cyclin-dependent kinase (CDK)–cyclin protein complex1. However, control of the G0-to-G1 transition is not completely understood. Here we demonstrate that p38 MAPK gamma (p38γ) acts as a CDK-like kinase and thus cooperates with CDKs, regulating entry into the cell cycle. p38γ shares high sequence homology, inhibition sensitivity and substrate specificity with CDK family members. In mouse hepatocytes, p38γ induces proliferation after partial hepatectomy by promoting the phosphorylation of retinoblastoma tumour suppressor protein at known CDK target residues. Lack of p38γ or treatment with the p38γ inhibitor pirfenidone protects against the chemically induced formation of liver tumours. Furthermore, biopsies of human hepatocellular carcinoma show high expression of p38γ, suggesting that p38γ could be a therapeutic target in the treatment of this disease
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