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排序方式: 共有477条查询结果,搜索用时 15 毫秒
151.
Amanda E. Brandon Bing M. Liao Barbara Diakanastasis Benjamin L. Parker Katy Raddatz Sophie A. McManus Liam OReilly Erica Kimber A. Gabrielle van der Kraan Dale Hancock Darren C. Henstridge Peter J. Meikle Gregory J. Cooney David E. James Saskia Reibe Mark A. Febbraio Trevor J. Biden Carsten Schmitz-Peiffer 《Cell metabolism》2019,29(1):183-191.e7
152.
153.
Christopher M. Vickery Richard Lockey Thomas M. Holder Leigh Thorne Katy E. Beck Christina Wilson Margaret Denyer John Sheehan Sarah Marsh Paul R. Webb Ian Dexter Angela Norman Emma Popescu Amanda Schneider Paul Holden Peter C. Griffiths Jane M. Plater Mark P. Dagleish Stuart Martin Glenn C. Telling Marion M. Simmons John Spiropoulos 《Journal of virology》2014,88(3):1830-1833
Several transgenic mouse models have been developed which facilitate the transmission of chronic wasting disease (CWD) of cervids and allow prion strain discrimination. The present study was designed to assess the susceptibility of the prototypic mouse line, Tg(CerPrP)1536+/−, to bovine spongiform encephalopathy (BSE) prions, which have the ability to overcome species barriers. Tg(CerPrP)1536+/− mice challenged with red deer-adapted BSE resulted in 90% to 100% attack rates, and BSE from cattle failed to transmit, indicating agent adaptation in the deer. 相似文献
154.
Emilie A. Rennie Berit Ebert Godfrey P. Miles Rebecca E. Cahoon Katy M. Christiansen Solomon Stonebloom Hoda Khatab David Twell Christopher J. Petzold Paul D. Adams Paul Dupree Joshua L. Heazlewood Edgar B. Cahoon Henrik Vibe Scheller 《The Plant cell》2014,26(8):3314-3325
Glycosyl inositol phosphorylceramide (GIPC) sphingolipids are a major class of lipids in fungi, protozoans, and plants. GIPCs are abundant in the plasma membrane in plants, comprising around a quarter of the total lipids in these membranes. Plant GIPCs contain unique glycan decorations that include a conserved glucuronic acid (GlcA) residue and various additional sugars; however, no proteins responsible for glycosylating GIPCs have been identified to date. Here, we show that the Arabidopsis thaliana protein INOSITOL PHOSPHORYLCERAMIDE GLUCURONOSYLTRANSFERASE1 (IPUT1) transfers GlcA from UDP-GlcA to GIPCs. To demonstrate IPUT1 activity, we introduced the IPUT1 gene together with genes for a UDP-glucose dehydrogenase from Arabidopsis and a human UDP-GlcA transporter into a yeast mutant deficient in the endogenous inositol phosphorylceramide (IPC) mannosyltransferase. In this engineered yeast strain, IPUT1 transferred GlcA to IPC. Overexpression or silencing of IPUT1 in Nicotiana benthamiana resulted in an increase or a decrease, respectively, in IPC glucuronosyltransferase activity in vitro. Plants in which IPUT1 was silenced accumulated IPC, the immediate precursor, as well as ceramides and glucosylceramides. Plants overexpressing IPUT1 showed an increased content of GIPCs. Mutations in IPUT1 are not transmitted through pollen, indicating that these sphingolipids are essential in plants. 相似文献
155.
The larval distribution of herbivorous insects play an important role in their development and hence future fitness. Here we study larval distribution of the critically endangered Sinai Baton Blue butterfly, Pseudophilotes sinaicus, which feeds exclusively on the buds and flowers of a single host plant, also endangered, the near-endemic Sinai thyme, Thymus decussatus. We studied the larval distribution over 131 plants, recording the size, quality and phenological stage of the plants along with the presence of beneficiaries. Larvae were found on plants with a high number of flowers, a relatively advanced flowering phenology and tending ants. This highlights the importance of the vitality and quality of the host plant to the spatial distribution of the Sinai Baton Blue. Future conservation plans might concentrate on improving the quality and quantity of the host plant in order to increase resources for this narrowly endemic species. 相似文献
156.
Marco Sealey‐Cardona Katy Schmidt Lars Demmel Tatjana Hirschmugl Tanja Gesell Gang Dong Graham Warren 《Traffic (Copenhagen, Denmark)》2014,15(6):613-629
The Sec16 homologue in Trypanosoma brucei has been identified and characterized. TbSec16 colocalizes with COPII components at the single endoplasmic reticulum exit site (ERES), which is next to the single Golgi stack in the insect (procyclic) form of this organism. Depletion of TbSec16 reduces the size of the ERES and the Golgi, and slows growth and transport of a secretory marker to the cell surface; conversely, overexpression of TbSec16 increases the size of the ERES and Golgi but has no effect on growth or secretion. Together these data suggest that TbSec16 regulates the size of the ERES and Golgi and this size is set for optimal growth of the organism. 相似文献
157.
Katy M Roach Heike Wulff Carol Feghali-Bostwick Yassine Amrani Peter Bradding 《Respiratory research》2014,15(1)
Background
Idiopathic pulmonary fibrosis is a common and invariably fatal disease with limited therapeutic options. Ca2+-activated KCa3.1 potassium channels play a key role in promoting TGFβ1 and bFGF-dependent profibrotic responses in human lung myofibroblasts (HLMFs). We hypothesised that KCa3.1 channel-dependent cell processes regulate HLMF αSMA expression via Smad2/3 signalling pathways.Methods
In this study we have compared the phenotype of HLMFs derived from non-fibrotic healthy control lungs (NFC) with cells derived from IPF lungs. HLMFs grown in vitro were examined for αSMA expression by immunofluorescence (IF), RT-PCR and flow cytommetry. Basal Smad2/3 signalling was examined by RT-PCR, western blot and immunofluorescence. Two specific and distinct KCa3.1 blockers (TRAM-34 200 nM and ICA-17043 [Senicapoc] 100 nM) were used to determine their effects on HLMF differentiation and the Smad2/3 signalling pathways.Results
IPF-derived HLMFs demonstrated increased constitutive expression of both α-smooth muscle actin (αSMA) and actin stress fibres, indicative of greater myofibroblast differentiation. This was associated with increased constitutive Smad2/3 mRNA and protein expression, and increased Smad2/3 nuclear localisation. The increased Smad2/3 nuclear localisation was inhibited by removing extracellular Ca2+ or blocking KCa3.1 ion channels with selective KCa3.1 blockers (TRAM-34, ICA-17043). This was accompanied by de-differentiation of IPF-derived HLMFs towards a quiescent fibroblast phenotype as demonstrated by reduced αSMA expression and reduced actin stress fibre formation.Conclusions
Taken together, these data suggest that Ca2+- and KCa3.1-dependent processes facilitate “constitutive” Smad2/3 signalling in IPF-derived fibroblasts, and thus promote fibroblast to myofibroblast differentiation. Importantly, inhibiting KCa3.1 channels reverses this process. Targeting KCa3.1 may therefore provide a novel and effective approach for the treatment of IPF and there is the potential for the rapid translation of KCa3.1-directed therapy to the clinic. 相似文献158.
Sebastian M. Lambert David R. Langley James A. Garnett Richard Angell Katy Hedgethorne Nicholas A. Meanwell Steve J. Matthews 《Protein science : a publication of the Protein Society》2014,23(6):723-734
New direct acting antivirals (DAAs) such as daclatasvir (DCV; BMS‐790052), which target NS5A function with picomolar potency, are showing promise in clinical trials. The exact nature of how these compounds have an inhibitory effect on HCV is unknown; however, major resistance mutations appear in the N‐terminal region of NS5A that include the amphipathic helix and domain 1. The dimeric symmetry of these compounds suggests that they act on a dimer of NS5A, which is also consistent with the presence of dimers in crystals of NS5A domain 1 from genotype 1b. Genotype 1a HCV is less potently affected by these compounds and resistance mutations have a greater effect than in the 1b genotypes. We have obtained crystals of domain 1 of the important 1a NS5A homologue and intriguingly, our X‐ray crystal structure reveals two new dimeric forms of this domain. Furthermore, the high solvent content (75%) makes it ideal for ligand‐soaking. Daclatasvir (DCV) shows twofold symmetry suggesting NS5A dimers may be of physiological importance and serve as potential binding sites for DCV. These dimers also allow for new conformations of a NS5A expansive network which could explain its operation on the membranous web. Additionally, sulfates bound in the crystal structure may provide evidence for the previously proposed RNA binding groove, or explain regulation of NS5A domain 2 and 3 function and phosphorylation, by domain 1. 相似文献
159.
Francisco I. Ramirez-Perez Angela L. Schenewerk Katy L. Coffman Christopher Foote Tieming Ji Rocio M. Rivera Luis A. Martinez-Lemus 《PloS one》2014,9(11)
Maternal obesity affects the incidence of cardiovascular disease and diabetes in offspring. Also the use of assisted reproductive technologies (ART) has been associated with cardiovascular deficiencies in offspring. Obese women often suffer from infertility and use ART to achieve a pregnancy, but the combined effects of maternal obesity and ART on cardiovascular health and incidence of diabetes in the offspring is not known. Here, we report the effects of the use of ART within an obesogenic environment, consisting of feeding a western diet (WD) to dams and offspring, on resistance artery function and presence of diabetes biomarkers in juvenile mice offspring. Our results indicate that WD and ART interacted to induce endothelial dysfunction in mesenteric resistance arteries isolated from 7-week-old mice offspring. This was determined by presence of a reduced acetylcholine-induced dilation compared to controls. The arteries from these WD-ART mice also had greater wall cross-sectional areas and wall to lumen ratios indicative of vascular hypertrophic remodeling. Of the diabetes biomarkers measured, only resistin was affected by a WD×ART interaction. Serum resistin was significantly greater in WD-ART offspring compared to controls. Diet and sex effects were observed in other diabetes biomarkers. Our conclusion is that in mice the use of ART within an obesogenic environment interacts to favor the development of endothelial dysfunction in the resistance arteries of juvenile offspring, while having marginal effects on diabetes biomarkers. 相似文献
160.
James Rooney Mark Heverin Alice Vajda Arlene Crampsie Katy Tobin Susan Byrne Anthony Staines Orla Hardiman 《PloS one》2014,9(5)