The \u3ci\u3eAPOA5\u3c/i\u3e rs662799 polymorphism is associated with dyslipidemia and the severity of coronary heart disease in Chinese women

Background: The APOA5 rs662799 polymorphism has been widely reported regarding its associations with the plasma lipid levels and the occurrence of coronary heart disease (CHD), whereas its relationship with the severity of CHD has not yet been explored. Methods: Four hundred and seventy-eight angiografically defined subjects (325 CHD patients and 153 CHD-free controls) were enrolled in this study. The rs662799 polymorphism was genotyped, and the fasting lipid data were collected for all participants. The severity of CHD was evaluated for the CHD patients by using Gensini scores. Results: The variant C allele of the rs662799 polymorphism was associated with lower levels of HDL-C in CHD-free women, and higher levels of TG and TG/HDL-C in women with CHD (P \u3c 0.05 for all). The C allele was associated with higher prevalence of dyslipidemia and higher levels of Gensini scores only in women (P \u3c 0.05 for both), but not in men. Multivariate linear regression analysis showed that the rs662799 polymorphism was independently associated with the Gensini scores in women after adjustment for other potential CHD risk factors (Beta = 0.157, 95 % CI: 0.017–0.298, P = 0.028). Conclusion: Our data indicate that the rs662799 polymorphism is associated with dyslipidemia and the severity of CHD in Chinese women

Glucagon regulates hepatic lipid metabolism via cAMP and Insig-2 signaling: implication for the pathogenesis of hypertriglyceridemia and hepatic steatosis

Insulin induced gene-2 (Insig-2) is an ER-resident protein that inhibits the activation of sterol regulatory element-binding proteins (SREBPs). However, cellular factors that regulate Insig-2 expression have not yet been identified. Here we reported that cyclic AMP-responsive element-binding protein H (CREBH) positively regulates mRNA and protein expression of a liver specific isoform of Insig-2, Insig-2a, which in turn hinders SREBP-1c activation and inhibits hepatic de novo lipogenesis. CREBH binds to the evolutionally conserved CRE-BP binding elements located in the enhancer region of Insig-2a and upregulates its mRNA and protein expression. Metabolic hormone glucagon and nutritional fasting activated CREBH, which upregulated expression of Insig-2a in hepatocytes and inhibited SREBP-1c activation. In contrast, genetic depletion of CREBH decreased Insig-2a expression, leading to the activation of SREBP-1c and its downstream lipogenic target enzymes. Compromising CREBH-Insig-2 signaling by siRNA interference against Insig-2 also disrupted the inhibitory effect of this signaling pathway on hepatic de novo triglyceride synthesis. These actions resulted in the accumulation of lipid droplets in hepatocytes and systemic hyperlipidemia. Our study identified CREBH as the first cellular protein that regulates Insig-2a expression. Glucagon activated the CREBH-Insig-2a signaling pathway to inhibit hepatic de novo lipogenesis and prevent the onset of hepatic steatosis and hypertriglyceridemia

Robust estimation of bacterial cell count from optical density

Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data

Growth and Development Responses of the Rhizome-Root System in <i>Pleioblastus pygmaeus</i> to Light Intensity

Light, as a primary source of energy, directly or indirectly influences virtually all morphological modifications occurring in both shoots and roots. A pot experiment was conducted to assess the growth patterns of one-year-old Pleioblastus pygmaeus plants’ rhizome-root systems and their responses to different light intensities from 11 March to 26 December 2016. The experiment design scheme was 3.87% (L1), 11.25% (L2), 20.25% (L3), 38.76% (L4), 60.70% (L5), and 100% full sunlight (control CK). The results indicated that along the growing period from March to December, eight of the eleven studied parameters of the rhizome-root system showed significant variability and diverse growth patterns. In addition, light intensity is a key factor for determining P. pygmaeus plants’ rhizome and root growth. Specifically, the light intensity had a significant, positive, and linear/or almost linear impact on the number of old and new rhizomes, old rhizome length, new rhizome diameter, as well as the culm root diameter. A nonlinear and positive relationship was found between light intensity and the listed three parameters, i.e., new rhizome length, new rhizome internode length, and rhizome root length. The value of the above-mentioned three parameters significantly increased when affected from 0% to 40–60% of full sunlight and then gradually increased until 100% of full sunlight. The ratio of aboveground dry weight to underground dry weight (A/U ratio) showed a single peak curve with increasing light intensity and presented the highest value under ca. 55% full sunlight. Furthermore, 40% full sunlight (equal to an average light of 2232 lux) might be the threshold for P. pygmaeus rhizome-root system growth. When the light intensity was below 40%, the generalized additive models (GAMs) predicted value of most studied parameters decreased to lower than zero. In conclusion, current study provides a solid basis for understanding the dynamic growth and development of P. pygmaeus rhizome-root system, and its responses to different light conditions, which could be used as inputs to P. pygmaeus plant cultivation

Stress Coupling Analysis and Failure Damage Evaluation of Wind Turbine Blades during Strong Winds

Blades in strong wind conditions are prone to various failures and damage that is due to the action of random variable amplitude loads. In this study, we analyze the failure of 1.5 MW horizontal axis wind turbine blades. The computational fluid dynamics unsteady calculation method is used to simulate the aerodynamic load distribution on the blade. Fluid–structure coupling methods are applied to calculate the blade stress. The results show that the equivalent stress of the blade is the largest when the azimuth angle is 30°, and the maximum equivalent stress is 20.60 MPa. There are obvious stress peaks in six sections, such as r/R = 0.10 (the span length of blade/the full length of the blade = 0.10). The frequency of damage that is caused by the stress in each area of the blade is determined based on the blade damage. The frequency of gel coat cracking in the blade tips and leaves is 77.78% and 22.22%, respectively, and the frequency of crack occurrence is 87.75%, 10.20% and 2.05%, respectively. By combining the stress concentration area and the damage results, the cause of blade damage is determined, which can replace the traditional inspection methods and improve the inspection efficiency

Stress Coupling Analysis and Failure Damage Evaluation of Wind Turbine Blades during Strong Winds

Blades in strong wind conditions are prone to various failures and damage that is due to the action of random variable amplitude loads. In this study, we analyze the failure of 1.5 MW horizontal axis wind turbine blades. The computational fluid dynamics unsteady calculation method is used to simulate the aerodynamic load distribution on the blade. Fluid&ndash;structure coupling methods are applied to calculate the blade stress. The results show that the equivalent stress of the blade is the largest when the azimuth angle is 30&deg;, and the maximum equivalent stress is 20.60 MPa. There are obvious stress peaks in six sections, such as r/R = 0.10 (the span length of blade/the full length of the blade = 0.10). The frequency of damage that is caused by the stress in each area of the blade is determined based on the blade damage. The frequency of gel coat cracking in the blade tips and leaves is 77.78% and 22.22%, respectively, and the frequency of crack occurrence is 87.75%, 10.20% and 2.05%, respectively. By combining the stress concentration area and the damage results, the cause of blade damage is determined, which can replace the traditional inspection methods and improve the inspection efficiency