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991.
Josef Mang Nina Korzeniewski Dimo Dietrich Verena Sailer Yanis Tolstov Sam Searcy Jost von Hardenberg Sven Perner Glen Kristiansen Alexander Marx Wilfried Roth Esther Herpel Carsten Grüllich Valentin Popeneciu Sascha Pahernik Boris Hadaschik Markus Hohenfellner Stefan Duensing 《Translational oncology》2015,8(6):487-496
We have recently shown that centrosomal protein 57 (CEP57) is overexpressed in a subset of human prostate cancers. CEP57 is involved in intracellular transport processes, and its overexpression causes mitotic defects as well as abnormal microtubule nucleation and bundling. In the present study, we further characterized the prognostic and functional role of CEP57 in prostate cancer. Unexpectedly, we found that high CEP57 expression is an independent prognostic factor for a more favorable biochemical recurrence-free survival in two large patient cohorts. To reconcile this finding with the ability of CEP57 to cause cell division errors and thus potentially promote malignant progression, we hypothesized that alterations of microtubule-associated transport processes, in particular nuclear translocation of the androgen receptor (AR), may play a role in our finding. However, CEP57 overexpression and microtubule bundling had, surprisingly, no effect on the nuclear translocation of the AR. Instead, we found a significant increase of cells with disarranged microtubules and a cellular morphology suggestive of a cytokinesis defect. Because mitotic dysfunction leads to a reduced daughter cell formation, it can explain the survival benefit of patients with increased CEP57 expression. In contrast, we show that a reduced expression of CEP57 is associated with malignant growth and metastasis. Taken together, our findings underscore that high CEP57 expression is associated with mitotic impairment and less aggressive tumor behavior. Because the CEP57-induced microtubule stabilization had no detectable effect on AR nuclear translocation, our results furthermore suggest that microtubule-targeting therapeutics used in advanced prostate cancer such as docetaxel may have modes of action that are at least in part independent of AR transport inhibition. 相似文献
992.
The visual cortex is able to extract disparity information through the use of binocular cells. This process is reflected by the Disparity Energy Model, which describes the role and functioning of simple and complex binocular neuron populations, and how they are able to extract disparity. This model uses explicit cell parameters to mathematically determine preferred cell disparities, like spatial frequencies, orientations, binocular phases and receptive field positions. However, the brain cannot access such explicit cell parameters; it must rely on cell responses. In this article, we implemented a trained binocular neuronal population, which encodes disparity information implicitly. This allows the population to learn how to decode disparities, in a similar way to how our visual system could have developed this ability during evolution. At the same time, responses of monocular simple and complex cells can also encode line and edge information, which is useful for refining disparities at object borders. The brain should then be able, starting from a low-level disparity draft, to integrate all information, including colour and viewpoint perspective, in order to propagate better estimates to higher cortical areas. 相似文献
993.
994.
Sascha N. Goonewardena Jeremy D. Kratz Hong Zong Ankur M. Desai Shengzhuang Tang Sarah Emery James R. Baker Baohua Huang 《Bioorganic & medicinal chemistry letters》2013,23(10):2872-2875
We have previously shown that methotrexate (MTX) conjugated to a cancer-specific poly amido amine (PAMAM) dendrimer has a higher therapeutic index than MTX alone. Unfortunately, these therapeutics have been difficult to advance because of the complicated syntheses and an incomplete understanding of the dendrimer properties. We wished to address these obstacles by using copper-free click chemistry to functionalize the dendrimer scaffolds and to exploring the effects of two dendrimer properties (the targeting ligand and drug linkage) on cytotoxicity. We conjugated either ester or amide-linker modified MTX to dendrimer scaffolds with or without folic acid (FA). Because of multivalency, the FA and MTX functionalized dendrimers had similar capacities to target the folate receptor on cancer cells. Additionally, we found that the ester- and amide-linker modified MTX compounds had similar cytotoxicity but the dendrimer–ester MTX conjugates were much more cytotoxic than the dendrimer–amide MTX conjugates. These results clarify the impact of these properties on therapeutic efficacy and will allow us to design more effective polymer therapeutics. 相似文献
995.
Nayla Jbeily Iris Suckert Falk A. Gonnert Benedikt Acht Clemens L. Bockmeyer Sascha D. Grossmann Markus F. Blaess Anja Lueth Hans-Peter Deigner Michael Bauer Ralf A. Claus 《Journal of lipid research》2013,54(2):410-424
Plasma secretion of acid sphingomyelinase is a hallmark of cellular stress
response resulting in the formation of membrane embedded ceramide-enriched lipid
rafts and the reorganization of receptor complexes. Consistently,
decompartmentalization of ceramide formation from inert sphingomyelin has been
associated with signaling events and regulation of the cellular phenotype.
Herein, we addressed the question of whether the secretion of acid
sphingomyelinase is involved in host response during sepsis. We found an
exaggerated clinical course in mice genetically deficient in acid
sphingomyelinase characterized by an increased bacterial burden, an increased
phagocytotic activity, and a more pronounced cytokine storm. Moreover, on a
functional level, leukocyte-endothelial interaction was found diminished in
sphingomyelinase-deficient animals corresponding to a distinct leukocytes’
phenotype with respect to rolling and sticking as well as expression of cellular
surface proteins. We conclude that hydrolysis of membrane-embedded
sphingomyelin, triggered by circulating sphingomyelinase, plays a pivotal role
in the first line of defense against invading microorganisms. This function
might be essential during the early phase of infection leading to an adaptive
response of remote cells and tissues. 相似文献
996.
Markus Pauly Sascha Gille Lifeng Liu Nasim Mansoori Amancio de Souza Alex Schultink Guangyan Xiong 《Planta》2013,238(4):627-642
One major component of plant cell walls is a diverse group of polysaccharides, the hemicelluloses. Hemicelluloses constitute roughly one-third of the wall biomass and encompass the heteromannans, xyloglucan, heteroxylans, and mixed-linkage glucan. The fine structure of these polysaccharides, particularly their substitution, varies depending on the plant species and tissue type. The hemicelluloses are used in numerous industrial applications such as food additives as well as in medicinal applications. Their abundance in lignocellulosic feedstocks should not be overlooked, if the utilization of this renewable resource for fuels and other commodity chemicals becomes a reality. Fortunately, our understanding of the biosynthesis of the various hemicelluloses in the plant has increased enormously in recent years mainly through genetic approaches. Taking advantage of this knowledge has led to plant mutants with altered hemicellulosic structures demonstrating the importance of the hemicelluloses in plant growth and development. However, while we are on a solid trajectory in identifying all necessary genes/proteins involved in hemicellulose biosynthesis, future research is required to combine these single components and assemble them to gain a holistic mechanistic understanding of the biosynthesis of this important class of plant cell wall polysaccharides. 相似文献
997.
Since 1993, members of the national wildlife society have undertaken annual surveys of large mammals in the Zambezi alluvial woodlands of Mana Pools National Park, Zimbabwe. Data are collected along 36 systematically‐arranged transects. We provide the first thorough assessment of the data from any survey within this long‐term project. The transect data from 2011 were analysed with DISTANCE software to assess if the data were suitable for determining the densities of large mammals using distance sampling techniques. Successful application of distance sampling depended on observers using printed, large‐scale, georeferenced satellite images onto which they mapped the location of animal groups detected. The assumptions of the distance sampling were well met and thus the 2011 survey provided reliable estimates of the densities of nine species of common large mammals on the Zambezi alluvium during the late dry season. Estimated density in this dry‐season concentration area varied from 3.6 km?2 for kudu, to 204 km?2 for impala. The precision of the estimates ranged from a coefficient of variation of 7.9% for elephant, to 25.5% for buffalo. For elephant, warthog and baboon, the morning and afternoon densities differed significantly. 相似文献
998.
N. Bouchemal-Chibani A. Lebrun C. Hervé du Penhoat M. Ghomi A. Laigle C. Derouet 《Journal of biomolecular structure & dynamics》2013,31(3):695-724
Abstract UV absorption, circular dichroïsm (CD) and 1H NMR, associated with Monte Carlo (MC) molecular structure simulations have been applied to the study of the trinucleoside diphosphate: r(ACC). The MC study which has been conducted as a function of temperature, is based on random variations of the nucleotide conformational angles, i.e. phosphodiester chain torsional angles and sugar pucker pseudorotational angles. All of the chemical bond lengths and valence angles remained fixed during the structural simulation, except those of the sugar pucker. Six different initial structures have been selected in order to explore the molecular conformational space as completely as possible. This simulation procedure led to distinct families of equilibrium conformations at 283,298 and 318 K. The thermodynamical parameters such as variations in entropy, enthalpy and also melting temperature (ΔS0 x, ΔH0 x and Tm) of the stacking (X) equilibrium were obtained from UV absorption and circular dichroïsm (CD) spectra recorded over a 80K temperature range. Chemical shifts (δ), vicinal coupling constants(3J k) and cross-relaxation rates (σk,l) of trimers were measured at 400.13 MHz over a range of concentrations (2–13mM) and temperatures (283–333K). Least-squares fitting of the experimental chemical shifts to simple models of association (A) and stacking equilibria allowed separation of the variations in the δ values (Δδx and ΔδA) due to either phenomenon. The three NMR data sets (Δδx, 3Jk,l and σk.l) were then evaluated for the minima conformers obtained with the MC simulations. Theoretical values of Δδx were estimated using the results of an ab initio study while the coupling constant data were simulated with Karplus-type equations. Finally, the relaxation data were simulated from the distance matrices using treatment for cases of both slow conformational exchange accompanied by rapid small-amplitude fluctuations about the minima structures. A consistent picture of the large amplitude deformations (torsional angle variation) of these trimers has emerged from the present study. Optimized conformational blends at 283, 296 and 318K were obtained by least-squares fitting of the experimental data to the theoretical ones, while considering the populations as adjustable parameters. As it would be expected, the right-handed helical conformation (A-RNA type) is found to be the major stacked species, in the temperature range of 283 to 318K. Limited evidence for bulged structures has been obtained, whereas novel reverse-stacked and half-stacked conformers also presented theoretical data compatible with the NMR observables of aqueous r(ACC). 相似文献
999.
Suzanne Geenen Franco B. du Preez Jacky L. Snoep Alison J. Foster Sunil Sarda J. Gerry Kenna Ian D. Wilson Hans V. Westerhoff 《Biochimica et Biophysica Acta (BBA)/General Subjects》2013
Background
Glutathione metabolism can determine an individual's ability to detoxify drugs. To increase understanding of the dynamics of cellular glutathione homeostasis, we have developed an experiment-based mathematical model of the kinetics of the glutathione network. This model was used to simulate perturbations observed when human liver derived THLE cells, transfected with human cytochrome P452E1 (THLE-2E1 cells), were exposed to paracetamol (acetaminophen).Methods
Human liver derived cells containing extra human cytochrome P4502E1 were treated with paracetamol at various levels of methionine and in the presence and absence of an inhibitor of glutamyl-cysteine synthetase (GCS). GCS activity was also measured in extracts. Intracellular and extracellular concentrations of substances involved in glutathione metabolism were measured as was damage to mitochondria and proteins. A bottom up mathematical model was made of the metabolic pathways around and including glutathione.Results
Our initial model described some, but not all the metabolite-concentration and flux data obtained when THLE-2E1 cells were exposed to paracetamol at concentrations high enough to affect glutathione metabolism. We hypothesized that the lack of correspondence could be due to upregulation of expression of glutamyl cysteine synthetase, one of the enzymes controlling glutathione synthesis, and confirmed this experimentally. A modified model which incorporated this adaptive response adequately described the observed changes in the glutathione pathway. Use of the adaptive model to analyze the functioning of the glutathione network revealed that a threshold input concentration of methionine may be required for effective detoxification of reactive metabolites by glutathione conjugation. The analysis also provided evidence that 5-oxoproline and ophthalmic acid are more useful biomarkers of glutathione status when analyzed together than when analyzed in isolation, especially in a new, model-assisted integrated biomarker strategy.Conclusion
A robust mathematical model of the dynamics of cellular changes in glutathione homeostasis in cells has been developed and tested in vitro.General significance
Mathematical models of the glutathione pathway that help examine mechanisms of cellular protection against xenobiotic toxicity and the monitoring thereof, can now be made. 相似文献1000.
Fan Lixian Xu Weijiang Jia Ting Netherlands Edward C. du Preez Louis H. 《Systematic parasitology》2020,97(6):639-647
Systematic Parasitology - Polystoma chaochiaoensis from the urinary bladder of the chaochiao frog Rana chaochiaoensis Liu was briefly described in a symposium abstract and presented at the Third... 相似文献