Caldesmon regulates the motility of vascular smooth muscle cells by modulating the actin cytoskeleton stability

<p>Abstract</p> <p>Background</p> <p>Migration of vascular smooth muscle cells (SMCs) from the media to intima constitutes a critical step in the development of proliferative vascular diseases. To elucidate the regulatory mechanism of vacular SMC motility, the roles of caldesmon (CaD) and its phosphorylation were investigated.</p> <p>Methods</p> <p>We have performed Transwell migration assays, immunofluorescence microscopy, traction microscopy and cell rounding assays using A7r5 cells transfected with EGFP (control), EGFP-wtCaD or phosphomimetic CaD mutants, including EGFP-A1A2 (the two PAK sites Ser452 and Ser482 converted to Ala), EGFP-A3A4 (the two Erk sites Ser497 and Ser527 converted to Ala), EGFP-A1234 (both PAK- and Erk-sites converted to Ala) and EGFP-D1234 (both PAK- and Erk-sites converted to Asp).</p> <p>Results</p> <p>We found that cells transfected with wtCaD, A1A2 or A3A4 mutants of CaD migrated at a rate approximately 50% more slowly than those EGFP-transfected cells. The migration activity for A1234 cells was only about 13% of control cells. Thus it seems both MAPK and PAK contribute to the motility of A7r5 cells and the effects are comparable and additive. The A1234 mutant also gave rise to highest strain energy and lowest rate of cell rounding. The migratory and contractile properties of these cells are consistent with stabilized actin cytoskeletal structures. Indeed, the A1234 mutant cells exhibited most robust stress fibers, whereas cells transfected with wtCaD or A3A4 (and A1A2) had moderately reinforced actin cytoskeleton. The control cells (transfected with EGFP alone) exhibited actin cytoskeleton that was similar to that in untransfected cells, and also migrated at about the same speed as the untransfected cells.</p> <p>Conclusions</p> <p>These results suggest that both the expression level and the level of MAPK- and/or PAK-mediated phosphorylation of CaD play key roles in regulating the cell motility by modulating the actin cytoskeleton stability in dedifferentiated vascular SMCs such as A7r5.</p

A critical review of resistance and oxidation mechanisms of Sb-oxidizing bacteria for the bioremediation of Sb(Ⅲ) pollution

Antimony (Sb) is a priority pollutant in many countries and regions due to its chronic toxicity and potential carcinogenicity. Elevated concentrations of Sb in the environmental originating from mining and other anthropogenic sources are of particular global concern, so the prevention and control of the source of pollution and environment remediation are urgent. It is widely accepted that indigenous microbes play an important role in Sb speciation, mobility, bioavailability, and fate in the natural environment. Especially, antimony-oxidizing bacteria can promote the release of antimony from ore deposits to the wider environment. However, it can also oxidize the more toxic antimonite [Sb(III)] to the less-toxic antimonate [Sb(V)], which is considered as a potentially environmentally friendly and efficient remediation technology for Sb pollution. Therefore, understanding its biological oxidation mechanism has great practical significance to protect environment and human health. This paper reviews studies of the isolation, identification, diversity, Sb(III) resistance mechanisms, Sb(III) oxidation characteristics and mechanism and potential application of Sb-oxidizing bacteria. The aim is to provide a theoretical basis and reference for the diversity and metabolic mechanism of Sb-oxidizing bacteria, the prevention and control of Sb pollution sources, and the application of environment treatment for Sb pollution

Impact of primary and secondary air supply intensity in stove on emissions of size-segregated particulate matter and carbonaceous aerosols from apple tree wood burning

In order to assess emission factors (EF) more accurately from household biomass burning, a series of laboratory controlled apple tree wood burning tests were conducted to measure the EFs of size-segregated particulate matter (PM) and carbonaceous aerosols. The controlled burning experiments were conducted with designed primary air (PA) and secondary air (SA) supply intensity. An optimum value of 7 m(3).h(-1) was found for SA, resulting the highest modified combustion efficiency (92.4 +/- 2.5%) as well as the lowest EFs of PM2.5 (0.13 +/- 0.01 g.MJ(-1)), OC (0.04 +/- 0.03 g.MJ(-1)) and EC (0.03 +/- 0.01 g.MJ(-1)). SA values of 7 and 10 m(3).h(-1) resulted the lowest EFs for all the different PM sizes. In a test with PA of 6 m(3.)h(-1) and SA of 7 m(3).h(-1), very low EFs were observed for 0C1 (8.2%), 0C2 (11.2%) and especially OP (Pyrolyzed OC) (0%, not detected), indicating nearly complete combustion under this air supply condition. Besides SA, higher PA was proved to have positive effects on PM and carbonaceous fraction emission reduction. For example, with a fixed SA of 1.5 m(3).h(-1), EFs of PM2.5 decreased from 0.64 to 0.27 g.MJ(-1) when PA increased from 6 to 15 m(3).h(-1) (P &lt; 0.05). Similar reductions were also observed in EFs of OC, EC and size segregated PM

analysis and visualization of natural threats against the security of electricity transmission system

Abstract Electricity is one of the crucial energies of modern society, but it is greatly threatened by various kinds of menaces, especially natural hazards. Although they rarely happen, their occurrence may hugely affect the operation of power system. In this paper, we firstly, according the impact on power systems, classify natural threats into two categories (natural disasters and extreme weather conditions) and several subcategories (geological, hydrological, meteorological and climatological). Then the changes in natural threats to power systems and their trends during recent decades are discussed, along with a review of events that pose natural threats to the power system. Finally, the georeferenced model based on the Italy transmission system for natural threats analysis is presented

Exploring the inorganic and organic nitrate aerosol formation regimes at a suburban site on the North China Plain

Nitrate-driven aerosol pollution frequently occurs during winter over the North China Plain (NCP). Extensive studies have focused on inorganic nitrate formation, but few have focused on organic nitrates in China, preduding a thorough understanding of the nitrogen cycle and nitrate aerosol formation. Here, the inorganic (NO3,inorg) and organic nitrate (NO3,org) formation regimes under aerosol liquid water (ALW) and aerosol acidity (pH) influences were investigated during winter over the NCP based on data derived from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). The campaign-averaged concentration of the total nitrate was 53 mu g m(3), with a 13% contribution from NO3,org, which exhibited a significantly decreased contribution with increasing haze episode evolution. The diurnal cycles of NO3,inorg and NO3,org were similar, with high concentrations during the nighttime at a high ALW level, revealing the important role of aqueous-phase processes. However, the correlations between the aerosol pH and NO3,inorg (R-2 = 0.13, P <0.01) and NO3,org (R-2 = 0.63, P <0.01) during polluted periods indicated a contrasting effect of aerosol pH on inorganic and organic nitrate formation. Our results provide a useful reference for smog chamber studies and promote a better understanding of organic nitrate formation via a nthropogenic emissions. (C) 2021 Elsevier B.V. All rights reserved.Peer reviewe

Atmospheric reactivity and oxidation capacity during summer at a suburban site between Beijing and Tianjin

Hydroxyl (OH) radicals, nitrate (NO3) radicals and ozone (O-3) play central roles in the troposphere because they control the lifetimes of many trace gases that result from anthropogenic and biogenic origins. To estimate the air chemistry, the atmospheric reactivity and oxidation capacity were comprehensively analyzed based on a parameterization method at a suburban site in Xianghe in the North China Plain from 6 July 2018 to 6 August 2018. The total OH, NO3 and O-3 reactivities at the site varied from 9.2 to 69.6, 0.7 to 27.5 and 3.3 x 10(-4 )to 1.8 x 10(-2) s(-1) with campaign-averaged values of 27.5 +/- 9.7, 2.2 +/- 2.6 and 1.2 +/- 1.7 x 10(-3) s(-1) (+/- standard deviation), respectively. NOx (NO + NO2) was by far the main contributor to the reactivities of the three oxidants, with average values of 43 %-99 %. Alkenes dominated the OH, NO3 and O-3 reactivities towards total nonmethane volatile organic compounds (NMVOCs), accounting for 42.9 %, 77.8 % and 94.0 %, respectively. The total OH, NO3 and O-3 reactivi- ties displayed similar diurnal variations with the lowest values during the afternoon but the highest values during rush hours, and the diurnal profile of NOx appears to be the major driver for the diurnal profiles of the reactivities of the three oxidants. A box model (a model to Simulate the concentrations of Organic vapors, Sulfuric Acid and Aerosols; SOSAA) derived from a column chemical transport model was used to simulate OH and NO3 concentrations during the observation period. The calculated atmospheric oxidation capacity (AOC) reached 4.5 x 10(8) molecules cm(-3) s(-1), with a campaign-averaged value of 7.8 x 10 7 molecules cm(-3) s(-1) dominated by OH (7.7 x 10(7) molecules cm(-3) s(-1), 98.2 %), 0 3 (1.2 x 10(6) molecules cm(-3) s(-1), 1.5 %) and NO3 (1.8 x 10(5) molecules cm(-3) s(-1), 0.3 %). Overall, the integration of OH, NO3 and O-3 reactivities analysis could provide useful insights for NMVOC pollution control in the North China Plain. We suggest that further studies, especially direct observations of OH and NO3 radical concentrations and their reactivities, are required to better understand trace gas reactivity and AOC.Peer reviewe

Brown Carbon Aerosol in Urban Xi’an, Northwest China: TheComposition and Light Absorption Properties

Light-absorbing organic carbon (i.e., brown carbon or BrC) in the atmospheric aerosol has significant contribution to light absorption and radiative forcing. However, the link between BrC optical properties and chemical composition remains poorly constrained. In this study, we combine spectrophotometric measurements and chemical analyses of BrC samples collected from July 2008 to June 2009 in urban Xi&#39;an, Northwest China. Elevated BrC was observed in winter (5 times higher than in summer), largely due to increased emissions from wintertime domestic biomass burning. The light absorption coefficient of methanol-soluble BrC at 365 nm (on average approximately twice that of water-soluble BrC) was found to correlate strongly with both parent polycyclic aromatic hydrocarbons (parent-PAHs, 27 species) and their carbonyl oxygenated derivatives (carbonyl-OPAHs, 15 species) in all seasons (r(2) &gt; 0.61). These measured parent-PAHs and carbonyl-OPAHs account for on average similar to 1.7% of the overall absorption of methanol-soluble BrC, about 5 times higher than their mass fraction in total organic carbon (OC, similar to 0.35%). The fractional solar absorption by BrC relative to element carbon (EC) in the ultraviolet range (300-400 nm) is significant during winter (42 +/- 18% for water-soluble BrC and 76 +/- 29% for methanol-soluble BrC), which may greatly affect the radiative balance and tropospheric photochemistry and therefore the climate and air quality