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Li A Ma Y Yu X Mort RL Lindsay CR Stevenson D Strathdee D Insall RH Chernoff J Snapper SB Jackson IJ Larue L Sansom OJ Machesky LM 《Developmental cell》2011,21(4):722-734
Highlights? Rac1 and the Scar/WAVE complex drive pseudopod-based motility of melanoblasts ? Rac1-depleted melanoblasts move using unique actin-based stubs and not blebs ? Rac1 controls pseudopod frequency but is dispensable for pseudopod formation ? Loss of Rac1 delays melanoblast cell-cycle progression and cytokinesis 相似文献
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Between 1988 and 1997, 72 mouse colonies and 38 rat colonies were examined for the presence of bacteria parasite infections. Among mouse and rat bacteria, high positive rates were observed with Proteus species (sp.), Pasteurella pneumotropica, Mycoplasma sp. and Pseudomonas aeruginosa. Concerning murine colonies, parasites frequently detected were Tritrichomonas sp., Syphacia sp., Aspiculuris tetraptera, Entamoeba muris, Spironucleus muris, Myobia musculi, Chilomastix sp. and Myocoptes musculinus. In rats, high rates were obtained with Syphacia sp., Tritrichomonas sp., Spironucleus muris, Entamoeba muris and Chilomastix sp. During the first part of the last decade, some agents such as Clostridium piliforme, Citrobacter sp., Mycoplasma sp., Pseudomonas aeruginosa, Myobia musculi, Radfordia ensifera, Spironucleus muris and Giardia muris were often found among rodents, and most of them were still present in 1997. At the time of our study, results point out that some agents are still persistent, even increasing during the same period. It is particularly the case for parasites such as Entamoeba muris and the oxyurids, but also for bacteria like Proteus sp. and Klebsiella pneumoniae. We can thus conclude that only very limited success has been achieved in preventing microbial and parasitic infections in mice and rats colonies. 相似文献
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Marc Lavigne Olivier Helynck Pascal Rigolet Rofia Boudria-Souilah Mireille Nowakowski Bruno Baron Sbastien Brül Sylviane Hoos Bertrand Raynal Lionel Guittat Claire Beauvineau Stphane Petres Anton Granzhan Jean Guillon Genevive Pratviel Marie-Paule Teulade-Fichou Patrick England Jean-Louis Mergny Hlne Munier-Lehmann 《Nucleic acids research》2021,49(13):7695
The multidomain non-structural protein 3 (Nsp3) is the largest protein encoded by coronavirus (CoV) genomes and several regions of this protein are essential for viral replication. Of note, SARS-CoV Nsp3 contains a SARS-Unique Domain (SUD), which can bind Guanine-rich non-canonical nucleic acid structures called G-quadruplexes (G4) and is essential for SARS-CoV replication. We show herein that the SARS-CoV-2 Nsp3 protein also contains a SUD domain that interacts with G4s. Indeed, interactions between SUD proteins and both DNA and RNA G4s were evidenced by G4 pull-down, Surface Plasmon Resonance and Homogenous Time Resolved Fluorescence. These interactions can be disrupted by mutations that prevent oligonucleotides from folding into G4 structures and, interestingly, by molecules known as specific ligands of these G4s. Structural models for these interactions are proposed and reveal significant differences with the crystallographic and modeled 3D structures of the SARS-CoV SUD-NM/G4 interaction. Altogether, our results pave the way for further studies on the role of SUD/G4 interactions during SARS-CoV-2 replication and the use of inhibitors of these interactions as potential antiviral compounds. 相似文献
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Bcl-xL is an anti-apoptotic protein that is frequently found to be overexpressed in non-small cell lung cancer leading to an inhibition of apoptosis and poor prognosis. Recently, the role of miRNAs in regulating apoptosis and cell survival during tumorigenesis has become evident, with cancer cells showing perturbed expression of various miRNAs. In this study, we utilized miRNA microarrays to determine if miRNA dysregulation in bcl-xL silenced lung adenocarcinoma cells could be involved in regulating cell death. Short interfering RNA-based transfection of A549 and SK-LU1 lung adenocarcinoma cells was successful in inducing a reduction in bcl-xL expression levels, resulting in a decrease in cell viability. A total of 10 miRNAs were found to be significantly differentially expressed when compared between siRNA-transfected and non-transfected cells including hsa-miR-181a, hsa-miR-769-5p, hsa-miR-361-5p, hsa-miR-1304 and hsa-miR-608. When overexpression studies on hsa-miR-608 was performed via transfection of miRNA mimics, cell death was found to be induced in A549 and SK-LU1 cells in comparison to untreated cells. This effect was reversed when knockdown studies involving anti-sense inhibitors were introduced. Combination of siRNA based silencing of bcl-xL (siBcl-xL) followed by anti-sense inhibitor transfection led to a decrease in the apoptotic population of A549 and SK-LU1 cells in comparison to cells only treated with siBcl-xL, illustrating the connection between bcl-xL, hsa-miR-608 and cell death. Gene target prediction analysis implicated the PI3K/AKT, WNT, TGF-β, and ERK signaling pathways as targets of bcl-xL induced miRNA alterations. We have demonstrated that bcl-xL silencing in A549 and SK-LU1 cells leads to the occurrence of cell death through the dysregulation of specific miRNAs. This study also provides a platform for anti-sense gene therapy whereby miRNA expression can be exploited to increase the apoptotic properties in lung adenocarcinoma cells. 相似文献
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Asma Alinsafi Nouceiba Adouani Fabrice Bline Thomas Lendormi Lionel Limousy Olivier Sire 《Process Biochemistry》2008,43(6):683-689
Laboratory-scale experiments were conducted to examine the N2O emission during the denitrification process. For each of the 6 runs carried out, synthetic effluent was fed in a 10 l batch mixed liquor to investigate the effect of nitrite on N2O emission and Helium was continuously bubbled through the reactor at constant rate (0.12 l/min) to favour N2O transfer and detection. An increasing COD/NO3−-N influent ratio from 3 to 7 was firstly applied (runs 1–3). Secondly, NO2− pulse additions were performed during run 4 and 5 (10 and 20 mg N/l, respectively). Finally, the reactor was fed with influent containing both NO2− and NO3−. We showed that N2O emission was detected shortly after NO2− accumulation, few minutes after the substrate feeding. The highest emission occurred at the lower COD/NO3−-N ratio (=3) and at the higher NO2− addition (20 mg N/l). In addition, the higher nitrogen conversion to N2O gas (14.4%) was obtained with an influent containing initially both NO2− and NO3−. Our results suggest a direct effect of the NO2− concentration on the N2O emission. We have also confirmed the inhibitory effect of NO2− concentration on N2O reduction. 相似文献
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An increased requirement for methionine by transformed rat liver epithelial cells in vitro 总被引:2,自引:0,他引:2
The growth of two normal and four transformed rat liver epithelial cell lines in a methionine-containing medium and a methionine-deficient medium supplemented with homocysteine was examined. The growth rates of the normal cells on the homocysteine-supplemented medium were approximately one-half the growth rates shown by the same cells in the methionine-containing medium. In contrast, three of the four transformed cell lines studied showed virtually no growth on the homocysteine-supplemented medium, although they grew quite rapidly on the methionine-containing medium. The fourth, transformed by N-methyl-N-nitrosourea, was able to grow on the homocysteine-supplemented medium at about one-third the rate as on the methionine-containing medium. Thus, transformed rat liver epithelial cells resemble other malignant cells in their reduced capacity to grow on homocysteine in the absence of methionine. 相似文献