排序方式: 共有63条查询结果,搜索用时 15 毫秒
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Renata Barsacchi Mariagrazia Coassin Matilde Maiorino Gualtiero Pelosi Cinzia Simonelli Fulvio Ursini 《Free radical biology & medicine》1989,6(6):573-579
Aim of this study was to confirm an increased free radical generation rate during ischemia-reoxygenation, by ultra-weak chemiluminescence detection at the surface of perfused rat heart. We observed that reoxygenation following 30 min global ischemia, induces an increase of ultraweak chemiluminescence emission in isolated perfused heart only if partial depletion of vitamin E is induced by dietary manipulation. Moreover, in normal diet fed rats, vitamin E is partially consumed during global ischemia, but not during reoxygenation. Since chemiluminescence increases during post-ischemic reperfusion, when vitamin E myocardial content is lowered, the most probable free radicals involved are the hydroperoxyl radical derivatives of lipids. These radicals, indeed, are known both to produce photoemission by disproportion and to react with vitamin E. On the other hand, the nature of the reaction that consumes vitamin E during ischemia is still obscure. Accordingly, the basal level of vitamin E myocardial content seems to be a key factor for protecting the heart against reoxygenation injury and its consumption during ischemia could be a determinant of myocardial sensitivity to oxidative stress during reperfusion. 相似文献
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Francesco Scavello Filippo Zeni Giuseppina Milano Federica Macrì Stefania Castiglione Estella Zuccolo Alessandro Scopece Giovanni Pezone Calogero C. Tedesco Patrizia Nigro Genny Degani Elisa Gambini Fabrizio Veglia Laura Popolo Giulio Pompilio Gualtiero I. Colombo Marco E. Bianchi Angela Raucci 《International journal of biological sciences》2021,17(10):2399
Myocardial aging increases the cardiovascular risk in the elderly. The Receptor for Advanced Glycation End-products (RAGE) is involved in age-related disorders. The soluble isoform (sRAGE) acts as a scavenger blocking the membrane-bound receptor activation. This study aims at investigating RAGE contribution to age-related cardiac remodeling.We analyzed the cardiac function of three different age groups of female Rage-/- and C57BL/6N (WT) mice: 2.5- (Young), 12- (Middle-age, MA) and 21-months (Old) old. While aging, Rage-/- mice displayed an increase in left ventricle (LV) dimensions compared to age-matched WT animals, with the main differences observed in the MA groups. Rage-/- mice showed higher fibrosis and a larger number of α-Smooth Muscle Actin (SMA)+ cells with age, along with increased expression of pro-fibrotic Transforming Growth Factor (TGF)-β1 pathway components. RAGE isoforms were undetectable in LV of WT mice, nevertheless, circulating sRAGE declined with aging and inversely associated with LV diastolic dimensions. Human cardiac fibroblasts stimulated with sRAGE exhibited a reduction in proliferation, pro-fibrotic proteins and TGF-beta Receptor 1 (TGFbR1) expression and Smad2-3 activation. Finally, sRAGE administration to MA WT animals reduced cardiac fibrosis.Hence, our work shows that RAGE associates with age-dependent myocardial changes and indicates sRAGE as an inhibitor of cardiac fibroblasts differentiation and age-dependent cardiac fibrosis. 相似文献
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Ilaria Naldi Monia Taranta Lisa Gherardini Gualtiero Pelosi Federica Viglione Settimio Grimaldi Luca Pani Caterina Cinti 《PloS one》2014,9(5)
Epigenetic events are critical contributors to the pathogenesis of cancer, and targeting epigenetic mechanisms represents a novel strategy in anticancer therapy. Classic demethylating agents, such as 5-Aza-2′-deoxycytidine (Decitabine), hold the potential for reprograming somatic cancer cells demonstrating high therapeutic efficacy in haematological malignancies. On the other hand, epigenetic treatment of solid tumours often gives rise to undesired cytotoxic side effects. Appropriate delivery systems able to enrich Decitabine at the site of action and improve its bioavailability would reduce the incidence of toxicity on healthy tissues. In this work we provide preclinical evidences of a safe, versatile and efficient targeted epigenetic therapy to treat hormone sensitive (LNCap) and hormone refractory (DU145) prostate cancers. A novel Decitabine formulation, based on the use of engineered erythrocyte (Erythro-Magneto-Hemagglutinin Virosomes, EMHVs) drug delivery system (DDS) carrying this drug, has been refined. Inside the EMHVs, the drug was shielded from the environment and phosphorylated in its active form. The novel magnetic EMHV DDS, endowed with fusogenic protein, improved the stability of the carried drug and exhibited a high efficiency in confining its delivery at the site of action in vivo by applying an external static magnetic field. Here we show that Decitabine loaded into EMHVs induces a significant tumour mass reduction in prostate cancer xenograft models at a concentration, which is seven hundred times lower than the therapeutic dose, suggesting an improved pharmacokinetics/pharmacodynamics of drug. These results are relevant for and discussed in light of developing personalised autologous therapies and innovative clinical approach for the treatment of solid tumours. 相似文献
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Elisa Sinigalia Gualtiero Alvisi Chiara V. Segré Beatrice Mercorelli Giulia Muratore Michael Winkler He-Hsuan Hsiao Henning Urlaub Alessandro Ripalti Susanna Chiocca Giorgio Palù Arianna Loregian 《PloS one》2012,7(11)
During the replication of human cytomegalovirus (HCMV) genome, the viral DNA polymerase subunit UL44 plays a key role, as by binding both DNA and the polymerase catalytic subunit it confers processivity to the holoenzyme. However, several lines of evidence suggest that UL44 might have additional roles during virus life cycle. To shed light on this, we searched for cellular partners of UL44 by yeast two-hybrid screenings. Intriguingly, we discovered the interaction of UL44 with Ubc9, an enzyme involved in the covalent conjugation of SUMO (Small Ubiquitin-related MOdifier) to cellular and viral proteins. We found that UL44 can be extensively sumoylated not only in a cell-free system and in transfected cells, but also in HCMV-infected cells, in which about 50% of the protein resulted to be modified at late times post-infection, when viral genome replication is accomplished. Mass spectrometry studies revealed that UL44 possesses multiple SUMO target sites, located throughout the protein. Remarkably, we observed that binding of UL44 to DNA greatly stimulates its sumoylation both in vitro and in vivo. In addition, we showed that overexpression of SUMO alters the intranuclear distribution of UL44 in HCMV-infected cells, and enhances both virus production and DNA replication, arguing for an important role for sumoylation in HCMV life cycle and UL44 function(s). These data report for the first time the sumoylation of a viral processivity factor and show that there is a functional interplay between the HCMV UL44 protein and the cellular sumoylation system. 相似文献
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Dynamic oscillation of translation and stress granule formation mark the cellular response to virus infection 总被引:1,自引:0,他引:1
A Ruggieri E Dazert P Metz S Hofmann JP Bergeest J Mazur P Bankhead MS Hiet S Kallis G Alvisi CE Samuel V Lohmann L Kaderali K Rohr M Frese G Stoecklin R Bartenschlager 《Cell host & microbe》2012,12(1):71-85
Virus infection-induced global protein synthesis suppression is linked to assembly of stress granules (SGs), cytosolic aggregates of stalled translation preinitiation complexes. To study long-term stress responses, we developed an imaging approach for extended observation and analysis of SG dynamics during persistent hepatitis C virus (HCV) infection. In combination with type 1 interferon, HCV infection induces highly dynamic assembly/disassembly of cytoplasmic SGs, concomitant with phases of active and stalled translation, delayed cell division, and prolonged cell survival. Double-stranded RNA (dsRNA), independent of viral replication, is sufficient to trigger these oscillations. Translation initiation factor eIF2α phosphorylation by protein kinase R mediates SG formation and translation arrest. This is antagonized by the upregulation of GADD34, the regulatory subunit of protein phosphatase 1 dephosphorylating eIF2α. Stress response oscillation is a general mechanism to prevent long-lasting translation repression and a conserved host cell reaction to multiple RNA viruses, which HCV may exploit to establish persistence. 相似文献
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Gualtiero Piccinini 《Biology & philosophy》1989,4(2):229-234
References to discussion 相似文献
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In this study a pilot-scale membrane bioreactor (MBR) and a conventional activated sludge plant (CASP), treating the same tannery wastewaters and in the same operating conditions, have been compared in order to evaluate the overall treatment efficiency, the presence and distribution of Gram negative bacteria and the kinetics of nitrifying bacteria. Process efficiency was evaluated in terms of organic and nitrogen compounds: the MBR showed a higher COD removal (+4%) and a more stable and complete nitrification. The Gram negative bacteria were detected by fluorescent in situ hybridization (FISH) with phylogenetic probes monitoring of alpha-, beta- and gamma-Proteobacteria, of the main ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria of the Nitrobacter and Nitrospira genera. The results showed that the main differences between the two sludges were: the higher abundance of alpha- and gamma-Proteobacteria in the MBR bioreactor and the presence of AOB aggregates only on the surfaces of MBR flocs. Finally, the titrimetric (pH-stat, DO-stat) tests showed similar values of the kinetic parameters of the nitrifiers both in MBR and CASP sludge. 相似文献
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Laura Castiglioni Francesca Colazzo Lucia Fontana Gualtiero I. Colombo Luca Piacentini Elisa Bono Giuseppina Milano Serena Paleari Annamaria Palermo Uliano Guerrini Elena Tremoli Luigi Sironi 《PloS one》2015,10(8)