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861.
Zhang Z Zhang ZY Fauser U Schluesener HJ 《Cellular and molecular life sciences : CMLS》2008,65(24):4055-4065
Valproic acid (VPA) is a short-chain branched fatty with anti-inflammatory, neuro-protective and axon-remodeling effects.
We investigated the effects of VPA in rats in which experimental autoimmune neuritis (EAN) had been induced (EAN rats). VPA
(300 mg/kg, intraperitoneally) administration to EAN rats once daily immediately following immunization significantly suppressed
mRNA levels of interferon-γ, tumor necrosis factor-α, interleukin (IL)-1β, IL-4, IL-6 and IL-17 in the lymph nodes of EAN
rats. In peripheral blood and sciatic nerves of EAN rats, Foxp3+ cells were increased but IL-17+ cells were decreased during VPA treatment. Furthermore, suppressive and therapeutic treatment with VPA greatly attenuated
both accumulation of macrophages, T cells and B cells, and demyelination in sciatic nerves, and greatly reduced the severity
and duration of EAN. In summary, our data demonstrated that VPA could effectively suppress inflammation in EAN, suggesting
that VPA could be a potent candidate for treatment of autoimmune neuropathies. 相似文献
862.
McGowan KA Li JZ Park CY Beaudry V Tabor HK Sabnis AJ Zhang W Fuchs H de Angelis MH Myers RM Attardi LD Barsh GS 《Nature genetics》2008,40(8):963-970
Mutations in genes encoding ribosomal proteins cause the Minute phenotype in Drosophila and mice, and Diamond-Blackfan syndrome in humans. Here we report two mouse dark skin (Dsk) loci caused by mutations in Rps19 (ribosomal protein S19) and Rps20 (ribosomal protein S20). We identify a common pathophysiologic program in which p53 stabilization stimulates Kit ligand expression, and, consequently, epidermal melanocytosis via a paracrine mechanism. Accumulation of p53 also causes reduced body size and erythrocyte count. These results provide a mechanistic explanation for the diverse collection of phenotypes that accompany reduced dosage of genes encoding ribosomal proteins, and have implications for understanding normal human variation and human disease. 相似文献
863.
864.
865.
J.S. Chen Z.R. Dong Y.Y. Li B.Z. Li Y. Xing W.Y. Shen G. Chen X.Q. Zhang J.X. Gao 《复旦学报(自然科学版)》2005,44(5):672-673
1 Introduction Optically active secondary alcohols are versatile building blocks for synthesis of unnatural biological active compounds and functional materials. Therefore, study on efficient synthesis of optically active alcohols is becoming an important subject in synthetic organic chemistry. Catalytic asymmetric reduction of carbonyl compounds is a practical method to create chiral alcohols. For the past decades, a large number of catalytic methods have been developed to achieve this goal. … 相似文献
866.
867.
Henao-Mejia J Elinav E Jin C Hao L Mehal WZ Strowig T Thaiss CA Kau AL Eisenbarth SC Jurczak MJ Camporez JP Shulman GI Gordon JI Hoffman HM Flavell RA 《Nature》2012,482(7384):179-185
Non-alcoholic fatty liver disease (NAFLD) is the hepatic manifestation of metabolic syndrome and the leading cause of chronic liver disease in the Western world. Twenty per cent of NAFLD individuals develop chronic hepatic inflammation (non-alcoholic steatohepatitis, NASH) associated with cirrhosis, portal hypertension and hepatocellular carcinoma, yet the causes of progression from NAFLD to NASH remain obscure. Here, we show that the NLRP6 and NLRP3 inflammasomes and the effector protein IL-18 negatively regulate NAFLD/NASH progression, as well as multiple aspects of metabolic syndrome via modulation of the gut microbiota. Different mouse models reveal that inflammasome-deficiency-associated changes in the configuration of the gut microbiota are associated with exacerbated hepatic steatosis and inflammation through influx of TLR4 and TLR9 agonists into the portal circulation, leading to enhanced hepatic tumour-necrosis factor (TNF)-α expression that drives NASH progression. Furthermore, co-housing of inflammasome-deficient mice with wild-type mice results in exacerbation of hepatic steatosis and obesity. Thus, altered interactions between the gut microbiota and the host, produced by defective NLRP3 and NLRP6 inflammasome sensing, may govern the rate of progression of multiple metabolic syndrome-associated abnormalities, highlighting the central role of the microbiota in the pathogenesis of heretofore seemingly unrelated systemic auto-inflammatory and metabolic disorders. 相似文献
868.
IDH1(R132H) mutation increases murine haematopoietic progenitors and alters epigenetics 总被引:1,自引:0,他引:1
M Sasaki CB Knobbe JC Munger EF Lind D Brenner A Brüstle IS Harris R Holmes A Wakeham J Haight A You-Ten WY Li S Schalm SM Su C Virtanen G Reifenberger PS Ohashi DL Barber ME Figueroa A Melnick JC Zúñiga-Pflücker TW Mak 《Nature》2012,488(7413):656-659
Mutations in the IDH1 and IDH2 genes encoding isocitrate dehydrogenases are frequently found in human glioblastomas and cytogenetically normal acute myeloid leukaemias (AML). These alterations are gain-of-function mutations in that they drive the synthesis of the ‘oncometabolite’ R-2-hydroxyglutarate (2HG). It remains unclear how IDH1 and IDH2 mutations modify myeloid cell development and promote leukaemogenesis. Here we report the characterization of conditional knock-in (KI) mice in which the most common IDH1 mutation, IDH1(R132H), is inserted into the endogenous murine Idh1 locus and is expressed in all haematopoietic cells (Vav-KI mice) or specifically in cells of the myeloid lineage (LysM-KI mice). These mutants show increased numbers of early haematopoietic progenitors and develop splenomegaly and anaemia with extramedullary haematopoiesis, suggesting a dysfunctional bone marrow niche. Furthermore, LysM-KI cells have hypermethylated histones and changes to DNA methylation similar to those observed in human IDH1- or IDH2-mutant AML. To our knowledge, our study is the first to describe the generation and characterization of conditional IDH1(R132H)-KI mice, and also the first report to demonstrate the induction of a leukaemic DNA methylation signature in a mouse model. Our report thus sheds light on the mechanistic links between IDH1 mutation and human AML. 相似文献
869.
Fei Z Rodin AS Andreev GO Bao W McLeod AS Wagner M Zhang LM Zhao Z Thiemens M Dominguez G Fogler MM Castro Neto AH Lau CN Keilmann F Basov DN 《Nature》2012,487(7405):82-85
Surface plasmons are collective oscillations of electrons in metals or semiconductors that enable confinement and control of electromagnetic energy at subwavelength scales. Rapid progress in plasmonics has largely relied on advances in device nano-fabrication, whereas less attention has been paid to the tunable properties of plasmonic media. One such medium--graphene--is amenable to convenient tuning of its electronic and optical properties by varying the applied voltage. Here, using infrared nano-imaging, we show that common graphene/SiO(2)/Si back-gated structures support propagating surface plasmons. The wavelength of graphene plasmons is of the order of 200 nanometres at technologically relevant infrared frequencies, and they can propagate several times this distance. We have succeeded in altering both the amplitude and the wavelength of these plasmons by varying the gate voltage. Using plasmon interferometry, we investigated losses in graphene by exploring real-space profiles of plasmon standing waves formed between the tip of our nano-probe and the edges of the samples. Plasmon dissipation quantified through this analysis is linked to the exotic electrodynamics of graphene. Standard plasmonic figures of merit of our tunable graphene devices surpass those of common metal-based structures. 相似文献
870.
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. 总被引:33,自引:0,他引:33
S Rust M Rosier H Funke J Real Z Amoura J C Piette J F Deleuze H B Brewer N Duverger P Denèfle G Assmann 《Nature genetics》1999,22(4):352-355
Tangier disease (TD) was first discovered nearly 40 years ago in two siblings living on Tangier Island. This autosomal co-dominant condition is characterized in the homozygous state by the absence of HDL-cholesterol (HDL-C) from plasma, hepatosplenomegaly, peripheral neuropathy and frequently premature coronary artery disease (CAD). In heterozygotes, HDL-C levels are about one-half those of normal individuals. Impaired cholesterol efflux from macrophages leads to the presence of foam cells throughout the body, which may explain the increased risk of coronary heart disease in some TD families. We report here refining of our previous linkage of the TD gene to a 1-cM region between markers D9S271 and D9S1866 on chromosome 9q31, in which we found the gene encoding human ATP cassette-binding transporter 1 (ABC1). We also found a change in ABC1 expression level on cholesterol loading of phorbol ester-treated THP1 macrophages, substantiating the role of ABC1 in cholesterol efflux. We cloned the full-length cDNA and sequenced the gene in two unrelated families with four TD homozygotes. In the first pedigree, a 1-bp deletion in exon 13, resulting in truncation of the predicted protein to approximately one-fourth of its normal size, co-segregated with the disease phenotype. An in-frame insertion-deletion in exon 12 was found in the second family. Our findings indicate that defects in ABC1, encoding a member of the ABC transporter superfamily, are the cause of TD. 相似文献