The alternatively spliced fibronectin CS1 isoform regulates IL-17A levels and mechanical allodynia after peripheral nerve injury.

BackgroundMechanical pain hypersensitivity associated with physical trauma to peripheral nerve depends on T-helper (Th) cells expressing the algesic cytokine, interleukin (IL)-17A. Fibronectin (FN) isoform alternatively spliced within the IIICS region encoding the 25-residue-long connecting segment 1 (CS1) regulates T cell recruitment to the sites of inflammation. Herein, we analyzed the role of CS1-containing FN (FN-CS1) in IL-17A expression and pain after peripheral nerve damage.MethodsMass spectrometry, immunoblotting, and FN-CS1-specific immunofluorescence analyses were employed to examine FN expression after chronic constriction injury (CCI) in rat sciatic nerves. The acute intra-sciatic nerve injection of the synthetic CS1 peptide (a competitive inhibitor of the FN-CS1/α4 integrin binding) was used to elucidate the functional significance of FN-CS1 in mechanical and thermal pain hypersensitivity and IL-17A expression (by quantitative Taqman RT-PCR) after CCI. The CS1 peptide effects were analyzed in cultured primary Schwann cells, the major source of FN-CS1 in CCI nerves.ResultsFollowing CCI, FN expression in sciatic nerve increased with the dominant FN-CS1 deposition in endothelial cells, Schwann cells, and macrophages. Acute CS1 therapy attenuated mechanical allodynia (pain from innocuous stimulation) but not thermal hyperalgesia and reduced the levels of IL-17A expression in the injured nerve. CS1 peptide inhibited the LPS- or starvation-stimulated activation of the stress ERK/MAPK pathway in cultured Schwann cells.ConclusionsAfter physical trauma to the peripheral nerve, FN-CS1 contributes to mechanical pain hypersensitivity by increasing the number of IL-17A-expressing (presumably, Th17) cells. CS1 peptide therapy can be developed for pharmacological control of neuropathic pain

To quantum mechanics through random fluctuations at the Planck time scale

We show that (in contrast to a rather common opinion) QM is not a complete theory. This is a statistical approximation of classical statistical mechanics on the {\it infinite dimensional phase space.} Such an approximation is based on the asymptotic expansion of classical statistical averages with respect to a small parameter $\alpha.$ Therefore statistical predictions of QM are only approximative and a better precision of measurements would induce deviations of experimental averages from quantum mechanical ones. In this note we present a natural physical interpretation of $\alpha$ as the time scaling parameter (between quantum and prequantum times). By considering the Planck time $t_P$ as the unit of the prequantum time scale we couple our prequantum model with studies on the structure of space-time on the Planck scale performed in general relativity, string theory and cosmology. In our model the Planck time $t_P$ is not at all the {\it "ultimate limit to our laws of physics"} (in the sense of laws of classical physics). We study random (Gaussian) infinite-dimensional fluctuations for prequantum times $s\leq t_P$ and show that quantum mechanical averages can be considered as an approximative description of such fluctuations.Comment: Discussion on the possibility to go beyond Q

Local redox buffering by carbon at low pressures and the formation of moissanite - natural SiC

International audienceGrains of natural SiC, moissanite, are encountered in various geological settings. According to thermodynamic calculations and high-pressure experiments, SiC formation requires very reducing conditions, approx. 6-10 orders of magnitude in fO2 more reducing than the present-day mantle redox state. SiC occurrences have motivated several studies but the required extremely reducing conditions remain a major inconsistency that has not been solved. It is shown here that such reducing conditions can be achieved during the ultimate steps of ascent of carbon-saturated melts, when pressure is lower than 100 bars. At these conditions, the redox buffering by carbon can impose fO2 similar to IW-6. Conditions favorable to SiC growth can therefore be reached around carbonaceous grains during the shallow emplacement of silicate melts or kimberlites and do not necessarily imply extremely localized oxygen-depleted regions in the mantle. Such reduced conditions can also explain the presence of elemental Si and iron-carbide inclusions in association with moissanite grains

Investigation of activated carbons by HRTEM, X-ray scattering and Raman spectra

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Microporosity and nanostructure in activated carbons: characterization by X-ray scattering, Raman spectrometry and HRTEM.

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Photoelectrocatalytic Properties of a Ti-Modified Nanocrystalline Hematite Film Photoanode

Photoelectrocatalytic oxidation of methanol, ethylene glycol, glycerol, and 5,6,7,8-tetrahydro-2-naphthol on thin-film nanocrystalline hematite electrodes fabricated by electrochemical deposition and promoted with spin-coated titanium has been studied. It is shown that the modification of hematite transforms it into material exhibiting high activity in the photoelectrochemical process of substrate oxidation upon illumination with light in the visible region of the spectrum. The highest activity is observed in the reaction of photoelectrocatalytic oxidation of glycerol. Results of intensity-modulated photocurrent spectroscopy (IMPS) suggest that the effect is due to an increased rate of charge transfer in the process of photoelectro-oxidation and efficient suppression of the recombination of generated electron-hole pairs. Therefore, thin-film photoanodes based on modified hematite are promising for practical application in the photooxidation of glycerol, a by-product of biofuel production, as well as in the photoelectrochemical degradation of other organic pollutants, including those formed during the production of pharmaceuticals

Photoelectrocatalytic Properties of a Ti-Modified Nanocrystalline Hematite Film Photoanode

Photoelectrocatalytic oxidation of methanol, ethylene glycol, glycerol, and 5,6,7,8-tetrahydro-2-naphthol on thin-film nanocrystalline hematite electrodes fabricated by electrochemical deposition and promoted with spin-coated titanium has been studied. It is shown that the modification of hematite transforms it into material exhibiting high activity in the photoelectrochemical process of substrate oxidation upon illumination with light in the visible region of the spectrum. The highest activity is observed in the reaction of photoelectrocatalytic oxidation of glycerol. Results of intensity-modulated photocurrent spectroscopy (IMPS) suggest that the effect is due to an increased rate of charge transfer in the process of photoelectro-oxidation and efficient suppression of the recombination of generated electron-hole pairs. Therefore, thin-film photoanodes based on modified hematite are promising for practical application in the photooxidation of glycerol, a by-product of biofuel production, as well as in the photoelectrochemical degradation of other organic pollutants, including those formed during the production of pharmaceuticals

Photoelectrocatalytic Activity of ZnO-Modified Hematite Films in the Reaction of Alcohol Degradation

Thin-film nanocrystalline hematite electrodes were fabricated by electrochemical deposition and loaded with electrodeposited zinc oxide in various amounts. Under visible light illumination, these electrodes demonstrate high activity in the photoelectrochemical degradation of methanol, ethylene glycol and, in particular, glycerol. Results of intensity-modulated photocurrent spectroscopy show that the photoelectrocatalysis efficiency is explained by the suppression of the electron–hole pair recombination and an increase in the rate of photo-induced charge transfer. Thus, zinc oxide can be considered an effective modifying additive for hematite photoanodes