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991.
Sonja Rittchen Katharina Jandl Ilse Lanz Bernhard Reiter Nerea Ferreirs Daniel Kratz Jrg Lindenmann Luka Brcic Thomas Brnthaler Reham Atallah Horst Olschewski Eva M. Sturm Akos Heinemann 《International journal of molecular sciences》2021,22(21)
Acute respiratory inflammation, most commonly resulting from bacterial or viral infection, is one of the leading causes of death and disability worldwide. The inflammatory lipid mediator prostaglandin D2 (PGD2) and its rate-limiting enzyme, hematopoietic PGD synthase (hPGDS), are well-known drivers of allergic pulmonary inflammation. Here, we sought to investigate the source and role of hPGDS-derived PGD2 in acute pulmonary inflammation. Murine bronchoalveolar monocytes/macrophages from LPS- but not OVA-induced lung inflammation released significant amounts of PGD2. Accordingly, human monocyte-derived macrophages expressed high basal levels of hPGDS and released significant levels of PGD2 after LPS/IFN-γ, but not IL-4 stimulation. Human peripheral blood monocytes secreted significantly more PGD2 than monocyte-derived macrophages. Using human precision-cut lung slices (PCLS), we observed that LPS/IFN-γ but not IL-4/IL-13 drive PGD2 production in the lung. HPGDS inhibition prevented LPS-induced PGD2 release by human monocyte-derived macrophages and PCLS. As a result of hPGDS inhibition, less TNF-α, IL-6 and IL-10 could be determined in PCLS-conditioned medium. Collectively, this dataset reflects the time-dependent release of PGD2 by human phagocytes, highlights the importance of monocytes and macrophages as PGD2 sources and suggests that hPGDS inhibition might be a potential therapeutic option for acute, non-allergic lung inflammation. 相似文献
992.
993.
Markus M. Knodel Arne Nägel Sebastian Reiter Martin Rupp Andreas Vogel Paul Targett-Adams Eva Herrmann Gabriel Wittum 《Computing and Visualization in Science》2015,17(5):235-253
Viruses are a major challenge to human health and prosperity. This holds true for various viruses which are either threatening Europe (like Dengue and Yellow fever) or which are currently causing big health problems like the hepatitis C virus (HCV). HCV causes chronic liver diseases like cirrhosis and cancer and is the main reason for liver transplantations. Exploring biophysical properties of virus-encoded components and viral life cycle is an exciting new area of current virological research. In this context, spatial resolution is an aspect that has not yet been received much attention despite strong biological evidence suggesting that intracellular spatial dependence is a crucial factor in the viral replication process. We are developing first spatio-temporal resolved models which mimic the behavior of the important components of virus replication within single liver cells. HCV replication is strongly associated to the intracellular Endoplasmatic Reticulum (ER) network. Here, we present the computational basis for the estimation of the diffusion constant of a central component of HCV genome (viral RNA) replication, namely the NS5a protein, on the surface of realistic reconstructed ER geometries. The basic surface partial differential equation (sPDE) evaluations are performed with UG4 using fast massively parallel multigrid solvers. The numerics of the simulations are studied in detail. Integrated concentrations within special subdomains correspond to experimental FRAP time series. In particular, we analyze the refinement stability in time and space for these integrated concentrations based on diffusion sPDEs upon large unstructured surface grids using heuristic values for the NS5a diffusion constant. This builds up a solid basis for future research not included in this presentation. e.g. the presented refinement stability analysis of the single sPDEs allows for parameter estimations for the NS5a diffusion constant. Our advanced Finite Volume/multigrid techniques also could be applied for studying life cycles of other viruses. 相似文献
994.
995.
Zinah N. Alabdali Emanuel Irizarry Mary P. Reiter Ali Ashraf Jennifer K. Lynch-Branzoi Adrian B. Mann 《应用聚合物科学杂志》2021,138(20):50442
In many applications, it is desirable for photocured adhesives to have high-mechanical strength in the cured state, but relatively low viscosity when liquid. This was achieved by adding less than 0.5 wt% hydroxyapatite and graphene to methyl methacrylate with diurethane dimethacrylate (UDMA-MMA). Nanoindentation shows hardness increasing by 30–40% and indentation modulus by >30% compared to UDMA-MMA on its own. Rheometry shows only a small increase in uncured viscosity for the liquid state. The additives affect the optical properties, mobility of free radicals, photocuring, and degree of conversion, the effects of which are seen in Fourier transform infrared and micro-Raman spectra. Thermographic images taken during curing show that the additives impact the photocuring process. In addition, changes in intermolecular bonding are seen in the vibrational spectra when the additives are present. The enhanced mechanical properties are attributed to the observed changes in photocuring and bonding. 相似文献
996.
997.
AS Parsadanian Y Cheng CR Keller-Peck DM Holtzman WD Snider 《Canadian Metallurgical Quarterly》1998,18(3):1009-1019
Bcl-xL is a death-inhibiting member of the Bcl-2/Ced9 family of proteins which either promote or inhibit apoptosis. Gene targeting has revealed that Bcl-xL is required for neuronal survival during brain development; however, Bcl-xL knock-out mice do not survive past embryonic day 13.5, precluding an analysis of Bcl-xL function at later stages of development. Bcl-xL expression is maintained at a high level postnatally in the CNS, suggesting that it may also regulate neuron survival in the postnatal period. To explore functions of Bcl-xL related to neuron survival in postnatal life, we generated transgenic mice overexpressing human Bcl-xL under the control of a pan-neuronal promoter. A line that showed strong overexpression in brainstem and a line that showed overexpression in hippocampus and cortex were chosen for analysis. We asked whether overexpression of Bcl-xL influences neuronal survival in the postnatal period by studying two injury paradigms that result in massive neuronal apoptosis. In the standard neonatal facial axotomy paradigm, Bcl-xL overexpression had substantial effects, with survival of 65% of the motor neurons 7 d after axotomy, as opposed to only 15% in nontransgenic littermates. To investigate whether Bcl-xL regulates survival of CNS neurons in the forebrain, we used a hypoxia-ischemia paradigm in neonatal mice. We show here that hypoxia-ischemia leads to substantial apoptosis in the hippocampus and cortex of wild-type neonatal mice. Furthermore, we show that overexpression of Bcl-xL is neuroprotective in this paradigm. We conclude that levels of Bcl-xL in postnatal neurons may be a critical determinant of their susceptibility to apoptosis. 相似文献
998.
WD Brown TR Oakes OT DeJesus MD Taylor AD Roberts RJ Nickles JE Holden 《Canadian Metallurgical Quarterly》1998,39(11):1884-1891
This article presents dosimetry based on the measurement of fluoro-DOPA activity in major tissues and in the bladder contents in humans after oral pretreatment with 100 mg carbidopa. METHODS: Bladder activity was measured continuously by external probe and calibrated using complete urine collections. Quantitative dynamic PET scans provided time-activity curves for the major organs. Bladder wall dosimetry was calculated using the methods of MIRD Pamphlet No. 14. Effective dose was calculated as described in ICRP Publication 60. RESULTS: Mean absorbed dose to the bladder wall surface per unit administered activity was 0.150 mGy/MBq (0.556 rad/mCi) with the realistic void schedule used in our studies. The dose was 0.027 mGy/MBq (0.101 rad/mCi) to the kidneys, 0.0197 mGy/MBq (0.0728 rad/mCi) to the pancreas, and 0.0186 mGy/MBq (0.0688 rad/mCi) to the uterus. Absorbed doses to other organs were an order of magnitude or more lower than the bladder, 0.009-0.015 mGy/MBq. The effective dose per unit administered activity was 0.0199 mSv/MBq (0.0735 rem/mCi.) CONCLUSION: Urinary excretion of fluoro-DOPA was altered significantly by pretreatment with carbidopa. In general, any manipulation of tracer metabolism in the body should be expected to produce changes in biodistribution and dosimetry. The largest radiation dose was to the bladder wall, for which our estimate was one-fifth of that from the original report. The methods used reflect realistic urinary physiology and typical use of this tracer. The principles of MIRD Pamphlet No. 14 should be used in planning studies using tracers excreted in the urine to minimize the absorbed dose. 相似文献
999.
R Mielke J Kessler B Szelies K Herholz K Wienhard WD Heiss 《Canadian Metallurgical Quarterly》1998,105(8-9):821-837
Normal aging of the brain is predominantly characterized by metabolic changes in the prefrontal cortex. While in middle age there is a trend to hyperfrontality, PET demonstrates in old age a decline of regional cerebral glucose metabolism in frontal areas. In progeric diseases, clinically apparent as premature aging, the metabolic pattern is similar like in normal aging but qualitatively more severe. In patients with the diagnosis of probable Alzheimer's disease (AD) hypometabolism in early dementia is typically present in heteromodal association areas. Hypometabolism then spreads to other cortical and subcortical regions suggesting a characteristic pattern of degeneration that reflects selective vulnerability within limbic-cortical networks. Synaptic plasticity, clinically apparent as cognitive reserve capacity, can be assessed by PET under specific cognitive activation. In AD it is reduced in comparison to age-matched normals and may be influenced by drugs giving trophic support to neurochemical systems. 相似文献
1000.
E Gaertner EH Zeren MV Fleming TV Colby WD Travis 《Canadian Metallurgical Quarterly》1996,20(1):36-45
Trichoderma reesei endoglucanase I (EGI) was used as a reporter enzyme for screening mutagenized yeast strains for increased ability to produce protein. Sixteen haploid Saccharomyces cerevisiae strains, transformed with a yeast multicopy vector pALK222, containing the EGI cDNA under the ADH1 promoter, produced EGI activity of 10(-5)-10(-4) g/l. On the average 93% of the total activity was secreted into the culture medium. Two strains with opposite mating types were mutagenized, and several mutants were isolated possessing up to 45-fold higher EGI activity. The best mutants were remutagenized and a second-generation mutant, strain 2804, with an additional twofold increase in EGI activity was selected. The mutant strain 2804 grew more slowly and reached a lower final cell density than the parental strain. In the selective minimal medium, the 2804 strain produced 40 mg/l immunoreactive EGI protein, but only 2% was active enzyme. In the rich medium the secreted EGI enzyme stayed active, but without selection pressure the EGI production ceased after 2 days of cultivation, when the strain 2804 had produced 10 mg/l of EGI. A sevenfold difference was found between the parental and the 2804 strain in their total EGI production relative to cell density. The difference in favour of the mutant strain was also detected on the mRNA level. The 2804 mutant was found to be more active than the parental strain also in the production of T. reesei cellulases, cellobiohydrolase I, and cellobiohydrolase II. 相似文献