MicroRNA Regulation of Oxidative Stress-Induced Cellular Senescence

Aging is a time-related process of functional deterioration at cellular, tissue, organelle, and organismal level that ultimately brings life to end. Cellular senescence, a state of permanent cell growth arrest in response to cellular stress, is believed to be the driver of the aging process and age-related disorders. The free radical theory of aging, referred to as oxidative stress (OS) theory below, is one of the most studied aging promoting mechanisms. In addition, genetics and epigenetics also play large roles in accelerating and/or delaying the onset of aging and aging-related diseases. Among various epigenetic events, microRNAs (miRNAs) turned out to be important players in controlling OS, aging, and cellular senescence. miRNAs can generate rapid and reversible responses and, therefore, are ideal players for mediating an adaptive response against stress through their capacity to fine-tune gene expression. However, the importance of miRNAs in regulating OS in the context of aging and cellular senescence is largely unknown. The purpose of our article is to highlight recent advancements in the regulatory role of miRNAs in OS-induced cellular senescence

Beyond milk : framing milk and oat-drink campaigns in Sweden

The growing demand for products that cause minimal environment impact and follow a sustainable production system allow new brands and marketing concepts to compete with traditional companies and well established products on the market. Through Facebook and Instagram, companies are able to connect with their consumers and present their own point of view on many different subjects. By analyzing 50 online publications from two Swedish companies, Oatly producing oat-drink and Arla producing milk, it was possible to identify the different frames used in their social-media campaigns when referring to environmental issues caused by especially, the milk production system. Besides, which frames they use when communicating social and cultural values in relation to milk production and consumption in Sweden. Through a content analysis and by applying the framing theory, it was possible to outline and interpret the standpoint Oatly and Arla shared with their online viewers and potential customers on their social media campaigns. The findings suggest that, milk in Sweden is culturally accepted and play an important role in the Swedish diet, especially considering its health benefits. While oat-drink challenge the conventional frames presented by the milk industry, being set as a sustainable option and an alternative to animal milk, focusing its marketing towards a newer generation that is interested in creating new habits and changing social patterns

Assembly and functional analysis of an S/MAR based episome with the cystic fibrosis transmembrane conductance regulator gene

Improving the efficacy of gene therapy vectors is still an important goal toward the development of safe and efficient gene therapy treatments. S/MAR (scaffold/matrix attached region)-based vectors are maintained extra-chromosomally in numerous cell types, which is similar to viral-based vectors. Additionally, when established as an episome, they show a very high mitotic stability. In the present study we tested the idea that addition of an S/MAR element to a CFTR (cystic fibrosis transmembrane conductance regulator) expression vector, may allow the establishment of a CFTR episome in bronchial epithelial cells. Starting from the observation that the S/MAR vector pEPI-EGFP (enhanced green fluorescence protein) is maintained as an episome in human bronchial epithelial cells, we assembled the CFTR vector pBQ-S/MAR. This vector, transfected in bronchial epithelial cells with mutated CFTR, supported long term wt CFTR expression and activity, which in turn positively impacted on the assembly of tight junctions in polarized epithelial cells. Additionally, the recovery of intact pBQ-S/MAR, but not the parental vector lacking the S/MAR element, from transfected cells after extensive proliferation, strongly suggested that pBQ-S/MAR was established as an episome. These results add a new element, the S/MAR, that can be considered to improve the persistence and safety of gene therapy vectors for cystic fibrosis pulmonary disease

Radiomic Gradient in Peritumoural Tissue of Liver Metastases: A Biomarker for Clinical Practice? Analysing Density, Entropy, and Uniformity Variations with Distance from the Tumour

The radiomic analysis of the tissue surrounding colorectal liver metastases (CRLM) enhances the prediction accuracy of pathology data and survival. We explored the variation of the textural features in the peritumoural tissue as the distance from CRLM increases. We considered patients with hypodense CRLMs >10 mm and high-quality computed tomography (CT). In the portal phase, we segmented (1) the tumour, (2) a series of concentric rims at a progressively increasing distance from CRLM (from one to ten millimetres), and (3) a cylinder of normal parenchyma (Liver-VOI). Sixty-three CRLMs in 51 patients were analysed. Median peritumoural HU values were similar to Liver-VOI, except for the first millimetre around the CRLM. Entropy progressively decreased (from 3.11 of CRLM to 2.54 of Liver-VOI), while uniformity increased (from 0.135 to 0.199, p < 0.001). At 10 mm from CRLM, entropy was similar to the Liver-VOI in 62% of cases and uniformity in 46%. In small CRLMs (≤30 mm) and responders to chemotherapy, normalisation of entropy and uniformity values occurred in a higher proportion of cases and at a shorter distance. The radiomic analysis of the parenchyma surrounding CRLMs unveiled a wide halo of progressively decreasing entropy and increasing uniformity despite a normal radiological aspect. Underlying pathology data should be investigated

Identification of microRNA-mRNA functional interactions in UVB-induced senescence of human diploid fibroblasts

BACKGROUND: Cellular senescence can be induced by a variety of extrinsic stimuli, and sustained exposure to sunlight is a key factor in photoaging of the skin. Accordingly, irradiation of skin fibroblasts by UVB light triggers cellular senescence, which is thought to contribute to extrinsic skin aging, although molecular mechanisms are incompletely understood. Here, we addressed molecular mechanisms underlying UVB induced senescence of human diploid fibroblasts. RESULTS: We observed a parallel activation of the p53/p21(WAF1) and p16(INK4a)/pRb pathways. Using genome-wide transcriptome analysis, we identified a transcriptional signature of UVB-induced senescence that was conserved in three independent strains of human diploid fibroblasts (HDF) from skin. In parallel, a comprehensive screen for microRNAs regulated during UVB-induced senescence was performed which identified five microRNAs that are significantly regulated during the process. Bioinformatic analysis of miRNA-mRNA networks was performed to identify new functional mRNA targets with high confidence for miR-15a, miR-20a, miR-20b, miR-93, and miR-101. Already known targets of these miRNAs were identified in each case, validating the approach. Several new targets were identified for all of these miRNAs, with the potential to provide new insight in the process of UVB-induced senescence at a genome-wide level. Subsequent analysis was focused on miR-101 and its putative target gene Ezh2. We confirmed that Ezh2 is regulated by miR-101 in human fibroblasts, and found that both overexpression of miR-101 and downregulation of Ezh2 independently induce senescence in the absence of UVB irradiation. However, the downregulation of miR-101 was not sufficient to block the phenotype of UVB-induced senescence, suggesting that other UVB-induced processes induce the senescence response in a pathway redundant with upregulation of miR-101. CONCLUSION: We performed a comprehensive screen for UVB-regulated microRNAs in human diploid fibroblasts, and identified a network of miRNA-mRNA interactions mediating UVB-induced senescence. In addition, miR-101 and Ezh2 were identified as key players in UVB-induced senescence of HDF

Daclatasvir plasma level and resistance selection in HIV patients with hepatitis C virus cirrhosis treated with daclatasvir, sofosbuvir, and ribavirin

ObjectivesEffective treatment with direct-acting antiviral drugs against hepatitis C virus (HCV) is a medical need in cirrhotic HIV–HCV co-infected patients.MethodsThis study investigated the plasma levels of daclatasvir (DCV) and ribavirin (RBV) in HIV–HCV co-infected subjects treated with DCV, sofosbuvir, and RBV. Drug concentrations were quantified using validated high-performance liquid chromatography methods with ultraviolet detection. The HCV non-structural protein 5A and non-structural protein 5B coding regions were analyzed by population-based sequencing.ResultsDCV was dosed at week 4 and at week 8 of treatment, and RBV at week 8. One patient had the lowest DCV level, corresponding to 32.7% of the overall median value of the other patients at week 4 and about 40% at week 8. The Y93H variant was detected in this subject at weeks 8, 16, and 20 of treatment, but not before treatment or at day 2, and the patient experienced virological failure. Another subject with the Y93H variant at baseline and appropriate DCV levels had HCV RNA <12 IU/ml at week 12 and undetectable at week 16.ConclusionsSub-optimal DCV drug levels allow the selection of resistance-associated variants and fail to contribute to antiviral activity. No definite reason for the low DCV level was found. Quantifying the drug is suggested in difficult-to-treat patients

RETRACE-3D PROJECT, a multidisciplinary approach for the construction of a 3D crustal model: first results and seismotectonic implications

The RETRACE-3D (centRal italy EarThquakes integRAted Crustal modEl) Project has been launched with the ambitious goal to build, as first result, a new, robust, 3D geological model of broad consensus of the area struck by the 2016-2018 Central Italy seismic sequencePublishedBologna3T. Sorgente sismica4T. Sismicità dell'Itali

Immunolocalization of galectin-3 in mouse public symphysis during pregnancy and post-partum

Orientador: Paulo Pinto JoazeiroDissertação (mestrado) - Universidade Estadual de Campinas, Instituto de BiologiaResumo: É reconhecido que a sínfise púbica de algumas espécies de mamíferos, incluindo camundongos, passa por transformações estruturais durante a prenhez e no período pós-parto. Estas transformações incluem o surgimento de um ligamento interpúbico e o amolecimento deste tecido nos dois últimos dias antes do parto. Este ligamento permite a separação dos ossos púbicos, garantindo a passagem segura do feto pelo canal de parto. Após o parto ocorre a involução deste ligamento. Ambos os períodos de remodelação tecidual envolvem grandes modificações da matriz extracelular e de seus componentes, bem como um balanço entre proliferação e morte celular programada. A galectina-3, uma lectina animal com especificidade de ligação por ß-galactosídeos, é uma proteína amplamente distribuída entre diferentes tipos de células e tecidos, podendo ser encontrada dentro das células tanto no núcleo quanto no citoplasma, ou ainda na superfície celular ou no espaço extracelular. Através de interações específicas com diversos ligantes intra e extracelulares, a galectina-3 participa de numerosos processos fisiológicos e patológicos, como por exemplo, desenvolvimento, reações imunes, controle do ciclo celular, apoptose e metástase. Este estudo teve como objetivo localizar a expressão de galectina-3 nas populações celulares que compõem esta articulação durante o período de prenhez, a fim de investigar seu possível envolvimento nos processos de remodelação da sínfise. Foi observado que a galectina-3 está presente em todas as populações celulares que compõem a sínfise púbica e o ligamento interpúbico de todos os grupos estudados. Além disso, a galectina-3 é co-localizada com a a-actina de músculo liso em alguns tipos celulares. A quantificação da detecção de galectina-3 nos permitiu observar que ela é expressa em diferentes concentrações durante o período estudado. Esses resultados nos permitiram concluir que a galectina-3 parece estar envolvida na remodelação da sínfise púbica, através de sua participação na ativação de células semelhantes a fibroblastos, no ciclo celular, na diferenciação e nos processos de morte celular programada.Abstract: It is recognized that the pubic symphysis of some mammal species, including mice, undergoes structural transformations during pregnancy and post-partum. These transformations include the emerging of an interpubic ligament and softening of this tissue in the two last days of pregnancy. This ligament allows the pelvic bones separation, warranting fetus self passage through the birth channel. After delivery this ligament involutes. Both periods of tissue remodeling involve changes in extracellular matrix and its components, as so a balance between cell proliferation and death. Galectin-3, an animal lectin with specificity for ß-galactosídes, is widely spread among different types of cells and tissues, thus being found inside the cells in the cytoplasm and in the nucleus, on cell surface or in the extracellular space. Through specific interactions with a variety of intra and extracellular ligands galectin-3 participates of numerous physiological and pathological processes, like for example, development, immune reactions, cell cycle control, apoptosis and metastasis. This research had the objective to localize galectin-3's expression in mouse pubic symphysis cells during pregnancy, and to investigate its involvement in the pubic remodeling process. It was observed that galectin-3 is present in all pubic cells populations of all of the studied groups. Besides that, galectin-3 is colocalized with a-smooth muscle actin in some cell types. Quantifying of galectin-3 detection revealed that this protein is expressed in different concentrations during the studied period. These results allowed us to conclude that galectin-3 seems to be involved in mouse pubic symphysis remodeling, probably working in the activation of fibroblast like cells, on cell cycle, on differentiation and in the processes of programmed cell death.MestradoBiologia CelularMestre em Biologia Celular e Estrutura

Effects of Air Pollution on Cellular Senescence and Skin Aging

The human skin is exposed daily to different environmental factors such as air pollutants and ultraviolet (UV) light. Air pollution is considered a harmful environmental risk to human skin and is known to promote aging and inflammation of this tissue, leading to the onset of skin disorders and to the appearance of wrinkles and pigmentation issues. Besides this, components of air pollution can interact synergistically with ultraviolet light and increase the impact of damage to the skin. However, little is known about the modulation of air pollution on cellular senescence in skin cells and how this can contribute to skin aging. In this review, we are summarizing the current state of knowledge about air pollution components, their involvement in the processes of cellular senescence and skin aging, as well as the current therapeutic and cosmetic interventions proposed to prevent or mitigate the effects of air pollution in the skin