2,479 research outputs found
Inhibition of platelet aggregation by olive oil phenols via cAMP-phosphodiesterase
The aim of the present study was to confirm that olive oil phenols reduce human platelet aggregability and to verify the hypothesis that cAMP- and cGMP- phosphodiesterases (PDE) could be one of the targets of the biological effect. Four extracts from oils characterized by a high phenol content (HPE), and low phenol levels (LPE) were prepared and analyzed quali- and quantitatively by HPLC-UV and electrospray ionization–MS/MS. Human washed platelets stimulated with thrombin were used for the aggregation assay. Human platelet cAMP-PDE and recombinant PDE5A1 were used as enzyme source. Platelet aggregation and enzyme activity were assayed in the presence of HPE, LPE and individual phenols. The phenol content of HPE ranged between 250 and 500 mg/kg, whereas the LPE content was 46 mg/kg. The compounds identified were hydroxytyrosol (HT), tyrosol (TY), oleuropein aglycone (OleA) and the flavonoids quercetin (QU), luteolin (LU) and apigenin (AP). OleA was the most abundant phenol (range 23·3 to 37·7 %) and LU was the most abundant flavonoid in the extracts. Oil extracts inhibited platelet aggregation with an 50% inhibitory concentration interval of 1·23–11·2 μg/ml. The inhibitory effect of individual compounds (10 μm) including homovanillyl alcohol (HVA) followed this order: OleA>LU>HT = TY = QU = HVA, while AP was inactive. All the extracts inhibited cAMP-PDE, while no significant inhibition of PDE5A1 (50μg/ml) was observed. All the flavonoids and OleA inhibited cAMP-PDE, whereas HT, TY, HVA (100 μm) were inactive. Olive oil extracts and part of its phenolic constituents inhibit platelet aggregation; cAMP-PDE inhibition is one mechanism through which olive oil phenols inhibit platelet aggregation
Nanoscale phase-engineering of thermal transport with a Josephson heat modulator
Macroscopic quantum phase coherence has one of its pivotal expressions in the
Josephson effect [1], which manifests itself both in charge [2] and energy
transport [3-5]. The ability to master the amount of heat transferred through
two tunnel-coupled superconductors by tuning their phase difference is the core
of coherent caloritronics [4-6], and is expected to be a key tool in a number
of nanoscience fields, including solid state cooling [7], thermal isolation [8,
9], radiation detection [7], quantum information [10, 11] and thermal logic
[12]. Here we show the realization of the first balanced Josephson heat
modulator [13] designed to offer full control at the nanoscale over the
phase-coherent component of thermal currents. Our device provides
magnetic-flux-dependent temperature modulations up to 40 mK in amplitude with a
maximum of the flux-to-temperature transfer coefficient reaching 200 mK per
flux quantum at a bath temperature of 25 mK. Foremost, it demonstrates the
exact correspondence in the phase-engineering of charge and heat currents,
breaking ground for advanced caloritronic nanodevices such as thermal splitters
[14], heat pumps [15] and time-dependent electronic engines [16-19].Comment: 6+ pages, 4 color figure
The RIG-I agonist M8 triggers cell death and natural killer cell activation in human papillomavirus-associated cancer and potentiates cisplatin cytotoxicity
Although the activation of innate immunity to treat a wide variety of cancers is gaining increasing attention, it has been poorly investigated in human papillomavirus (HPV)-associated malignancies. Because these tumors harbor a severely impaired cGAS-STING axis, but they still retain a largely functional RIG-I pathway, another critical mediator of adaptive and innate immune responses, we asked whether RIG-I activation by the 5'ppp-RNA RIG-I agonist M8 would represent a therapeutically viable option to treat HPV+ cancers. Here, we show that M8 transfection of two cervical carcinoma-derived cell lines, CaSki and HeLa, both expressing a functional RIG-I, triggers intrinsic apoptotic cell death, which is significantly reduced in RIG-I KO cells. We also demonstrate that M8 stimulation potentiates cisplatin-mediated cell killing of HPV+ cells in a RIG-I dependent manner. This combination treatment is equally effective in reducing tumor growth in a syngeneic pre-clinical mouse model of HPV16-driven cancer, where enhanced expression of lymphocyte-recruiting chemokines and cytokines correlated with an increased number of activated natural killer (NK) cells in the tumor microenvironment. Consistent with a role of RIG-I signaling in immunogenic cell killing, stimulation of NK cells with conditioned medium from M8-transfected CaSki boosted NK cell proliferation, activation, and migration in a RIG-I-dependent tumor cell-intrinsic manner. Given the highly conserved molecular mechanisms of carcinogenesis and genomic features of HPV-driven cancers and the remarkably improved prognosis for HPV+ oropharyngeal cancer, targeting RIG-I may represent an effective immunotherapeutic strategy in this setting, favoring the development of de-escalating strategies
IRST SiPM characterizations and application studies
This paper reports on work undertaken, in collaboration with ITC-IRST at Trento, to characterize and test the silicon photomultiplers produced by them, with a view to their future application in high energy and astrophysics experiments. Results of static and dynamic measurents with various IRST devices under controlled climatic conditions, together with measurements with SiPMs from other distributors are reported and discussed with emphasis on progress in the understanding of operational principles and the reduction of noise. Results from the test beam application of the SiPMs are also reported and future plans are discusse
Development of technique for testing the long-term stability of silicon microstrip detectors
An automatic multi-channel set-up prototype for simultaneous testing of the Long-Term Stability (LTS)
*
of more
than ten detectors is described. The Inner Tracking System of the ALICE experiment will include about two thousand
Double-Sided Microstrip Detectors (DSMD). Efficient automatic measurement techniques are crucial for the
LTS test, because the corresponding test procedure should be performed on each detector and requires long times, at
least two days. By using special adapters for supporting and connecting the bare DSMDs, failing detectors can be
screened out before module assembly, thus minimizing the cost. Automated probe stations developed for a special
purpose or for microelectronics industry are used for measuring physical static DSMD characteristics and check
good-to-bad element ratio for DSMD. However, automated (or semi-automatic) test benches for studying LTS or
testing DSMD long-term stability before developing a detecting module are absent.Важная часть тестирования детектора и процедура определения гарантии качества состоит в изучении долговременной стабильности основных характеристик (ДСХ) детекторов, включая исследование эффектов влияния окружающей среды, таких как влажность или температура. В данной работе описаны метод тестирования и автоматический многоканальный стенд, специально разработанный для одновременного тестирования ДСХ более чем десяти детекторовВажлива частина тестування детектора і процедури визначення гарантії якості складається у вивченні
довгострокової стабільності основних характеристик (ДСХ) детекторів, включаючи дослідження ефектів
впливу навколишнього середовища, таких як вологість або температура. У даній роботі описані метод
тестування та автоматичний стенд, спеціально розроблений для одночасного тестування ДСХ більш ніж
десяти детекторів
CCRL2 Expression by Specialized Lung Capillary Endothelial Cells Controls NK-cell Homing in Lung Cancer
Patterns of receptors for chemotactic factors regulate the homing of leukocytes to tissues. Here we report that the CCRL2/chemerin/CMKLR1 axis represents a selective pathway for the homing of natural killer (NK) cells to the lung. C-C motif chemokine receptor-like 2 (CCRL2) is a nonsignaling seven-transmembrane domain receptor able to control lung tumor growth. CCRL2 constitutive or conditional endothelial cell targeted ablation, or deletion of its ligand chemerin, were found to promote tumor progression in a Kras/p53Flox lung cancer cell model. This phenotype was dependent on the reduced recruitment of CD27- CD11b+ mature NK cells. Other chemotactic receptors identified in lung-infiltrating NK cells by single-cell RNA sequencing (scRNA-seq), such as Cxcr3, Cx3cr1, and S1pr5, were found to be dispensable in the regulation of NK-cell infiltration of the lung and lung tumor growth. scRNA-seq identified CCRL2 as the hallmark of general alveolar lung capillary endothelial cells. CCRL2 expression was epigenetically regulated in lung endothelium and it was upregulated by the demethylating agent 5-aza-2'-deoxycytidine (5-Aza). In vivo administration of low doses of 5-Aza induced CCRL2 upregulation, increased recruitment of NK cells, and reduced lung tumor growth. These results identify CCRL2 as an NK-cell lung homing molecule that has the potential to be exploited to promote NK cell-mediated lung immune surveillance
A Temporal Threshold for Formaldehyde Crosslinking and Fixation
Formaldehyde crosslinking is in widespread use as a biological fixative for microscopy and molecular biology. An assumption behind its use is that most biologically meaningful interactions are preserved by crosslinking, but the minimum length of time required for an interaction to become fixed has not been determined.Using a unique series of mutations in the DNA binding protein MeCP2, we show that in vivo interactions lasting less than 5 seconds are invisible in the microscope after formaldehyde fixation, though they are obvious in live cells. The stark contrast between live cell and fixed cell images illustrates hitherto unsuspected limitations to the fixation process. We show that chromatin immunoprecipitation, a technique in widespread use that depends on formaldehyde crosslinking, also fails to capture these transient interactions.Our findings for the first time establish a minimum temporal limitation to crosslink chemistry that has implications for many fields of research
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