100 research outputs found

    Touch of chemokines

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    Chemoattractant cytokines or chemokines constitute a family of structurally related proteins found in vertebrates, bacteria, or viruses. So far, 48 chemokine genes have been identified in humans, which bind to around 20 chemokine receptors These receptors belong to the seven transmembrane G-protein-coupled receptor family. Chemokines and their receptors were originally studied for their role in cellular trafficking of leukocytes during inflammation and immune surveillance. It is now known that they exert different functions under physiological conditions such as homeostasis, development, tissue repair, and angiogenesis but also under pathological disorders including tumorigenesis, cancer metastasis, inflammatory, and autoimmune diseases. Physicochemical properties of chemokines and chernokine receptors confer the ability to homo- and hetero-oligornerize. Many efforts are currently performed in establishing new therapeutically compounds able to target the chemokine/chemokine receptor system. In this review, we are interested in the role of chemokines in inflammatory disease and leukocyte trafficking with a focus on vascular inflammatory diseases, the operating synergism, and the emerging therapeutic approaches of chemokines

    Translational opportunities of single-cell biology in atherosclerosis

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    The advent of single-cell biology opens a new chapter for understanding human biological processes and for diagnosing, monitoring, and treating disease. This revolution now reaches the field of cardiovascular disease (CVD). New technologies to interrogate CVD samples at single-cell resolution are allowing the identification of novel cell communities that are important in shaping disease development and direct towards new therapeutic strategies. These approaches have begun to revolutionize atherosclerosis pathology and redraw our understanding of disease development. This review discusses the state-of-the-art of single-cell analysis of atherosclerotic plaques, with a particular focus on human lesions, and presents the current resolution of cellular subpopulations and their heterogeneity and plasticity in relation to clinically relevant features. Opportunities and pitfalls of current technologies as well as the clinical impact of single-cell technologies in CVD patient care are highlighted, advocating for multidisciplinary and international collaborative efforts to join the cellular dots of CVD

    Vibrational-rotational structure of the silane molecule in the band of v2+v4 (F2)

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    In recent years, extensive theoretical studies have been carried out on the silane molecule, namely their vibrational-rotational structure. In this work, we continue our research series and focus on the 28SiD4 isotopologue. The IR-spectrum of the silane molecule was recorded in the range 1250-1450 cm-1 (pentad region) on Bruker IFS 120HR Fourier interferometer. The P, Q, and R branches with Jmax up to 17 were assigned, and spectroscopic constants of the v2+v4 (F2) band were derived for 28SiD4. As a result, a set of spectroscopic parameters was obtained which describe the vibrational-rotational structure of the silane molecule close to the experimental uncertainties

    Сравнительная характеристика армированных пластиков, применительно к космической отрасли

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    Extracellular Vesicles as Biomarkers in Cardiovascular Disease; Chances and Risks

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    The field of extracellular vesicles (EV) is rapidly expanding, also within cardiovascular diseases. Besides their exciting roles in cell-to-cell communication, EV have the potential to serve as excellent biomarkers, since their counts, content, and origin might provide useful information about the pathophysiology of cardiovascular disorders. Various studies have already indicated associations of EV counts and content with cardiovascular diseases. However, EV research is complicated by several factors, most notably the small size of EV. In this review, the advantages and drawbacks of EV-related methods and applications as biomarkers are highlighted
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