Numerical simulation research of vortex-induced vibrations of the long circular cylinders with high mass-ratio

The two-degrees-of-freedom vortex-induced vibrations (VIV) of the long circular cylinders with high mass-ratio are numerically simulated with the software ANSYS/CFX. The VIV characteristic of the cylinder is analyzed in the different conditions (Ur = 3, 5, 6, 8, 10). When Ur is 5, 6, 8 and 10, the conclusion is different from the vortex-induced vibrations of the cylinder with low mass-ratio. When Ur is 3, the frequency of the drag force on the cylinder is twice of that of the lift force and the in-line VIV frequency of the cylinder is twice of that of the cross-flow VIV. The in-line VIV amplitude of the cylinder is much smaller than the cross-flow VIV amplitude. The motion trace is the crescent. When Ur is 5 and 6, the frequency ratio between the drag force and lift force is still 2, but the main in-line VIV frequency of the cylinder is mainly the same as that of the cross-flow VIV and the secondary in-line VIV frequency is equal to the frequency of the drag force. The in-line VIV amplitude is still very small compared with the cross-flow VIV amplitude. When Ur is up to 8 and 10, the in-line VIV frequency of the cylinder is the same as the main frequency of the cross-flow VIV which is close to the inherent frequency of the cylinder and is different from the frequency of the drag force or lift force. But the secondary cross-flow VIV frequency of the cylinder is equal to the frequency of the lift force. The amplitude ratio between in-line VIV and cross-flow VIV is about 0.5. When Ur is 5, 6, 8 and 10, the motion trace is mainly the oval

Statistical delay distribution analysis on high-speed railway trains

Published by SpringerOpen, Heidelber

Fractalkine is expressed in the human ovary and increases progesterone biosynthesis in human luteinised granulosa cells

Background: Recent evidence from rodent ovaries has demonstrated expression of fractalkine and the existence of fractalkine receptor, and showed that there is a significant increase in steroidogenesis in response to fractalkine, yet the role of fractalkine and CX3CR1 in the human ovary is still unknown. This study aimed to determine the expression levels of fractalkine and CX3CR1 in the human ovary and to investigate their roles in sexual hormone biosynthesis by human luteinising granulosa cells. This is the first detailed report of fractalkine and CX3CR1 expression and function in the human ovary. Methods: Fractalkine and CX3CR1 expression levels were measured by immunohistochemistry using ovarian tissue from pathological specimens from five individuals. Granulosa cells were obtained from patients during IVF treatment. They were cultured and treated with increasing doses of hCG with or without fractalkine. Media were collected to detect estradiol and progesterone by chemiluminescence. StAR, 3 beta HSD and CYP11A expression were determined in granulosa cells treated with or without fractalkine by real-time RT-PCR. Results: Fractalkine and CX3CR1 were expressed in the human ovary and in luteinising granulosa cells. However, fractalkine expression was stronger in luteinising granulosa cells. Treatment with fractalkine augmented hCG stimulation of progesterone production in a dose-dependent manner with concomitant increases in transcript levels for key steroidogenic enzymes (StAR, 3-beta HSD and CYP11A) but had no effect on estradiol biosynthesis(P < 0.05). Conclusions: Fractalkine and CX3CR1 were found to express in human ovary and luteinising granulosa cells. Fractalkine can increase the biosynthesis of progesterone in a dose-dependent manner by enhancing transcript levels of key steroidogenic enzymes.http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000292939500001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Endocrinology & MetabolismReproductive BiologySCI(E)PubMed2ARTICLE95

Overexpression of the Tomato Pollen Receptor Kinase LePRK1 Rewires Pollen Tube Growth to a Blebbing Mode

The tubular growth of a pollen tube cell is crucial for the sexual reproduction of flowering plants. LePRK1 is a pollen-specific and plasma membrane–localized receptor-like kinase from tomato (Solanum lycopersicum). LePRK1 interacts with another receptor, LePRK2, and with KINASE PARTNER PROTEIN (KPP), a Rop guanine nucleotide exchange factor. Here, we show that pollen tubes overexpressing LePRK1 or a truncated LePRK1 lacking its extracellular domain (LePRK1ΔECD) have enlarged tips but also extend their leading edges by producing “blebs.” Coexpression of LePRK1 and tomato PLIM2a, an actin bundling protein that interacts with KPP in a Ca2+-responsive manner, suppressed these LePRK1 overexpression phenotypes, whereas pollen tubes coexpressing KPP, LePRK1, and PLIM2a resumed the blebbing growth mode. We conclude that overexpression of LePRK1 or LePRK1ΔECD rewires pollen tube growth to a blebbing mode, through KPP- and PLIM2a-mediated bundling of actin filaments from tip plasma membranes. Arabidopsis thaliana pollen tubes expressing LePRK1ΔECD also grew by blebbing. Our results exposed a hidden capability of the pollen tube cell: upon overexpression of a single membrane-localized molecule, LePRK1 or LePRK1ΔECD, it can switch to an alternative mechanism for extension of the leading edge that is analogous to the blebbing growth mode reported for Dictyostelium and for Drosophila melanogaster stem cells.Fil: Gui, Cai Ping. Chinese Academy of Sciences; República de ChinaFil: Dong, Xin. Chinese Academy of Sciences; República de ChinaFil: Liu, Hai Kuan. Chinese Academy of Sciences; República de ChinaFil: Huang, Wei Jie. Chinese Academy of Sciences; República de ChinaFil: Zhang, Dong. Chinese Academy of Sciences; República de ChinaFil: Wang, Shu Jie. Chinese Academy of Sciences; República de ChinaFil: Barberini, María Laura. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Gao, Xiao Yan. Chinese Academy of Sciences; República de ChinaFil: Muschietti, Jorge Prometeo. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Biodiversidad y Biología Experimental; ArgentinaFil: McCormick, Sheila. University of California at Berkeley; Estados UnidosFil: Tang, Wei Hua. Chinese Academy of Sciences; República de China. University of California at Berkeley; Estados Unido

Disruption of Microtubules Post-Virus Entry Enhances Adeno-Associated Virus Vector Transduction

Perinuclear retention of viral particles is a poorly understood phenomenon observed during many virus infections. In this study, we investigated whether perinuclear accumulation acts as a barrier to limit recombinant adeno-associated virus (rAAV) transduction. After nocodazole treatment to disrupt microtubules at microtubule-organization center (MT-MTOC) after virus entry, we observed higher rAAV transduction. To elucidate the role of MT-MTOC in rAAV infection and study its underlying mechanisms, we demonstrated that rAAV's perinuclear localization was retained by MT-MTOC with fluorescent analysis, and enhanced rAAV transduction from MT-MTOC disruption was dependent on the rAAV capsid's nuclear import signals. Interestingly, after knocking down RhoA or inhibiting its downstream effectors (ROCK and Actin), MT-MTOC disruption failed to increase rAAV transduction or nuclear entry. These data suggest that enhancement of rAAV transduction is the result of increased trafficking to the nucleus via the RhoA-ROCK-Actin pathway. Ten-fold higher rAAV transduction was also observed by disrupting MT-MTOC in brain, liver, and tumor in vivo. In summary, this study indicates that virus perinuclear accumulation at MT-MTOC is a barrier-limiting parameter for effective rAAV transduction and defines a novel defense mechanism by which host cells restrain viral invasion

Statistical delay distribution analysis on high-speed railway trains

The focus of this study is to explore the statistical distribution models of high-speed railway (HSR) train delays. Based on actual HSR operational data, the delay causes and their classification, delay frequency, number of affected trains, and space–time delay distributions are discussed. Eleven types of delay events are classified, and a detailed analysis of delay distribution for each classification is presented. Models of delay probability delay probability distribution for each cause are proposed. Different distribution functions, including the lognormal, exponential, gamma, uniform, logistic, and normal distribution, were selected to estimate and model delay patterns. The most appropriate distribution, which can approximate the delay duration corresponding to each cause, is derived. Subsequently, the Kolmogorov–Smirnov (K–S) test was used to test the goodness of fit of different train delay distribution models and the associated parameter values. The test results show that the distribution of the test data is consistent with that of the selected models. The fitting distribution models show the execution effect of the timetable and help in finding out the potential conflicts in real-time train operations. Document type: Articl