Implications of C1q/TNF-related protein superfamily in patients with coronary artery disease.

The C1q complement/TNF-related protein superfamily (CTRPs) displays differential effects on the regulation of metabolic homeostasis, governing cardiovascular function. However, whether and how they may serve as predictor/pro-diagnosis factors for assessing the risks of coronary artery disease (CAD) remains controversial. Therefore, we performed a clinical study to elaborate on the implication of CTRPs (CTRP1, CTRP5, CTRP7, and CTRP15) in CAD. CTRP1 were significantly increased, whereas CTRP7 and CTRP15 levels were decreased in CAD patients compared to the non-CAD group. Significant differences in CTRP1 levels were discovered between the single- and triple-vascular-vessel lesion groups. ROC analysis revealed that CTRP7 and CTRP15 may serve as CAD markers, while CTRP1 may serve as a marker for the single-vessel lesion of CAD. CTRP1 and CTRP5 can serve as markers for the triple-vessel lesion. CTRP1 may serve as an independent risk predictor for triple-vessel lesion, whereas CTRP15 alteration may serve for a single-vessel lesion of CAD. CTRP1 may serve as a novel superior biomarker for diagnosis of severity of vessel-lesion of CAD patients. CTRP7, CTRP15 may serve as more suitable biomarker for the diagnosis of CAD patients, whereas CTRP5 may serve as an independent predictor for CAD. These findings suggest CTRPs may be the superior predictive factors for the vascular lesion of CAD and represent novel therapeutic targets against CAD

Low Loss and Magnetic Field-tuned Superconducting THz Metamaterial

Superconducting terahertz (THz) metamaterial (MM) made from superconducting Nb film has been investigated using a continuous-wave THz spectroscopy with a superconducting split-coil magnet. The obtained quality factors of the resonant modes at 132 GHz and 450 GHz are about three times as large as those calculated for a metal THz MM operating at 1 K, which indicates that superconducting THz MM is a very nice candidate to achieve low loss performance. In addition, the magnetic field-tuning on superconducting THz MM is also demonstrated, which offer an alternative tuning method apart from the existed electric, optical and thermal tuning on THz MM

Influence of hole-drilling diameter on aluminum alloy residual stress measurement

A hole-drilling method and finite element (FEM) numerical simulation are used to estimate the residual stress of aluminum alloy welding joints. In order to study the influence of hole diameter on measurement accuracy, a group of experiments are conducted. Experiment results show that the measuring error can be the minimal when the drilling hole diameter is 4 mm. Residual stress of 2219-T87 aluminum alloy welding joints under this optimal hole diameter are obtained. The distribution of the residual stress from the welding seam to the outward is first tensile stress and then compressive stress. And the maximum residual stress is 123.2 MPa

Loss of Asxl1 Alters Self-Renewal and Cell Fate of Bone Marrow Stromal Cell, Leading to Bohring-Opitz-like Syndrome in Mice

De novo ASXL1 mutations are found in patients with Bohring-Opitz syndrome, a disease with severe developmental defects and early childhood mortality. The underlying pathologic mechanisms remain largely unknown. Using Asxl1-targeted murine models, we found that Asxl1 global loss as well as conditional deletion in osteoblasts and their progenitors led to significant bone loss and a markedly decreased number of bone marrow stromal cells (BMSCs) compared with wild-type littermates. Asxl1(-/-) BMSCs displayed impaired self-renewal and skewed differentiation, away from osteoblasts and favoring adipocytes. RNA-sequencing analysis revealed altered expression of genes involved in cell proliferation, skeletal development, and morphogenesis. Furthermore, gene set enrichment analysis showed decreased expression of stem cell self-renewal gene signature, suggesting a role of Asxl1 in regulating the stemness of BMSCs. Importantly, re-introduction of Asxl1 normalized NANOG and OCT4 expression and restored the self-renewal capacity of Asxl1(-/-) BMSCs. Our study unveils a pivotal role of ASXL1 in the maintenance of BMSC functions and skeletal development

Effects of Time Delay and Noise on Asymptotic Stability in Human Quiet Standing Model

A human quiet standing stability is discussed in this paper. The model under consideration is proposed to be a delayed differential equation (DDE) with multiplicative white noise perturbation. The method of the center manifold is generalized to reduce a delayed differential equation to a two-dimensional ordinary differential equation, to study delay-induced instability or Hopf bifurcation. Then, the stochastic average method is employed to obtain the Itô equation. Thus, the top Lyapunov exponent is calculated and the necessary and sufficient condition of the asymptotic stability in views of probability one is obtained. The results show that the exponent is related to not only the strength of noise but also the delay, namely, the reaction speed of brain. The effect of the strength of noise on the human quiet standing losing stability is weak for a small delay. With the delay increasing, such effect becomes stronger and stronger. A small change in the strength of noise may destabilize the quiet standing for a large delay. It implies that a person with slow reaction is easy to lose the stability of his/her quiet standing

6,7,8,14,15,16-Hexaphenyldibenzo[c,gh]naphtho[3,2,1,8-pqra]tetraphene-5,13-dione dichloromethane monosolvate

The main mol­ecule of the title compound, C66H38O2·CH2Cl2, is centrosymmetric, the asymmetric unit is composed of two half-mol­ecules, located on inversion centers, and a mol­ecule of dichloro­methane. The large π-conjugated fused polycyclic system including eight six-membered rings is nearly planar, with r.m.s. deviations of 0.2114 and 0.2081 Å in the two independent mol­ecules

Synthesis of N-(3-(4-[11C]methylpiperazin-1-yl)−1-(5-methylpyridin-2-yl)−1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide as a new potential PET agent for imaging of IRAK4 enzyme in neuroinflammation

The reference standard N-(3-(4-methylpiperazin-1-yl)−1-(5-methylpyridin-2-yl)−1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide (9) and its demethylated precursor N-(1-(5-methylpyridin-2-yl)−3-(piperazin-1-yl)−1H-pyrazol-5-yl)pyrazolo[1,5-α]pyrimidine-3-carboxamide (8) were synthesized from pyrazolo[1,5-a]pyrimidine-3-carboxylic acid and ethyl 2-cyanoacetate with overall chemical yield 13% in nine steps and 14% in eight steps, respectively. The target tracer N-(3-(4-[11C]methylpiperazin-1-yl)−1-(5-methylpyridin-2-yl)−1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide ([11C]9) was prepared from its precursor with [11C]CH3OTf through N-[11C]methylation and isolated by HPLC combined with SPE in 50–60% radiochemical yield, based on [11C]CO2 and decay corrected to EOB. The radiochemical purity was >99%, and the specific activity at EOB was 370–1110 GBq/μmol