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61.
目的:了解神经激肽-2受体(NK-2R)在正常胰腺和慢性胰腺炎组织中的表达, 探讨其表达与慢性胰腺炎疼痛发生的关系。方法:25个慢性胰腺炎标本取自慢性胰腺炎手术, 男性18例, 女性7例, 正常胰腺组织取自20个器官捐献者, 男性11例, 女性9例。应用实时定量逆转录聚合酶链反应技术, 检测正常胰腺和慢性胰腺炎组织NK-2R的mRNA水平, 应用Western blot技术检测NK-2R的蛋白水平, 应用免疫组织化学方法进行NK-2R的组织学定位。将NK-2R mRNA水平与疼痛的程度、发作频率和持续时间进行分析, 寻找其中的相关性。结果:与正常胰腺相比, 慢性胰腺炎组织中NK-2R mRNA和蛋白都过度表达, NK-2R mRNA水平与疼痛的程度(r=0.59, P<0.01)、发作频率(r=0.51, P<0.05)和持续时间(r=0.53, P<0.05)明显相关。免疫组化检查显示, NK-2R的表达主要位于胰腺腺泡、胰腺导管、神经纤维和炎性细胞。结论:慢性胰腺炎组织中NK-2R的mRNA和蛋白表达水平都明显上调, 扰乱了神经激肽的作用环节;NK-2R的过度表达与疼痛发生有关。 相似文献
62.
Enzyme Immunoassay Detecting Teichoic and Lipoteichoic Acids versus Cerebrospinal Fluid Culture and Latex Agglutination for Diagnosis of Streptococcus pneumoniae Meningitis
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Kristin Stuertz Imke Merx Helmut Eiffert Erich Schmutzhard Michael Mder Roland Nau 《Journal of clinical microbiology》1998,36(8):2346-2348
A newly developed enzyme immunoassay (EIA) was used to detect the presence of pneumococcal teichoic and lipoteichoic acids in cerebrospinal fluid (CSF) from patients with Streptococcus pneumoniae meningitis who were being treated with antibiotics. All initial CSF samples, which on culture grew S. pneumoniae, were positive in the EIA. A total of 14 subsequent culture-negative samples gave clear signals in the EIA up to day 15 after the onset of antibiotic treatment. For 11 CSF specimens, culture, microscopy, and latex agglutination were negative while the EIA detected pneumococcal antigens. The EIA did not react either with CSF of patients with meningitis caused by bacteria other than S. pneumoniae or by viral pathogens. In conclusion, this EIA can be a valuable tool for the diagnosis of S. pneumoniae meningitis from CSF samples in cases in which prior antimicrobial therapy minimizes the usefulness of culture or other antigen detection tests. 相似文献
63.
Werner Haas Jacqueline Mathur-Rochat Helmut Pohlit Markus Nabholz Harald Von Boehmer 《European journal of immunology》1980,10(11):828-834
Various procedures were used to derive continuously growing cytotoxic T lymphocyte (CTL) clones from a primary culture containing responder cells from immunized mice and 3-(p-sulfophenyldiazo)-4-hydroxylphenyl acetic acid (SP)-or fluorescein isothiocyanate (FL)-coupled stimulator cells. It seems likely that CTL have to undergo some change, possibly genetic, to be able to grow continuously in T cell growth factor conditioned medium in the absence of any stimulator or filler cells. The most convenient and reliable procedure to generate CTL clones with different specificities was to establish from several aliquots of a primary culture cell populations continuously growing in medium conditioned with T cell growth factor(s). Clones with different specificities segregated in the different populations. SP-and FL-specific CTL clones restricted to H-2Kk, and H-2Dd and two FL-specific CTL clones with no apparent H-2 restriction are described. 相似文献
64.
Ulrike Fuhrmann Karsten Parczyk Michael Klotzbücher Helmut Klocker A. C. B. Cato 《Journal of molecular medicine (Berlin, Germany)》1998,76(7):512-524
Antihormones are by definition antagonists of steroid hormone action. They interact with the ligand binding domains of steroid
hormone receptors and competitively inhibit the action of the receptors by mechanisms that are not quite understood. In certain
cases antihormones also exhibit agonistic activity especially in connection with certain naturally occurring receptor mutants.
These observations together with findings of indiscriminate interaction of antihormones with several classes of steroid receptors
have necessitated a search of more effective and reliable antihormones. Recent advances in the resolution of the crystal structure
of the ligand binding domains of certain members of the steroid receptor family and identification of non-liganded activation
of steroid receptors have produced considerable information that can be harnessed into a fruitful search for a new generation
of antihormones.
Received: 19 June 1997 / Accepted: 10 October 1997 相似文献
65.
11-Methacryloylaminoundecanoic acid ( 1 ) was esterified with the monoalcohols isobutyl alcohol, cyclohexanol, DL -menthol, cholesterol, testosterone and an excess of 12-hydroxylauric acid in the presence of lipase as catalyst. The kinetics of the esterification reactions were followed by 1H NMR spectroscopy and the results were correlated with sterical effects. The monomers were polymerized radically. The monomeric 12-hydroxylauric acid oligoester 11 as well as its homopolymer 12 were characterized by DSC and viscosity measurements. 相似文献
66.
Autoimmunity and inflammation due to a gain-of-function mutation in phospholipase C gamma 2 that specifically increases external Ca2+ entry 总被引:3,自引:0,他引:3
Yu P Constien R Dear N Katan M Hanke P Bunney TD Kunder S Quintanilla-Martinez L Huffstadt U Schröder A Jones NP Peters T Fuchs H de Angelis MH Nehls M Grosse J Wabnitz P Meyer TP Yasuda K Schiemann M Schneider-Fresenius C Jagla W Russ A Popp A Josephs M Marquardt A Laufs J Schmittwolf C Wagner H Pfeffer K Mudde GC 《Immunity》2005,22(4):451-465
The identification of specific genetic loci that contribute to inflammatory and autoimmune diseases has proved difficult due to the contribution of multiple interacting genes, the inherent genetic heterogeneity present in human populations, and a lack of new mouse mutants. By using N-ethyl-N-nitrosourea (ENU) mutagenesis to discover new immune regulators, we identified a point mutation in the murine phospholipase Cg2 (Plcg2) gene that leads to severe spontaneous inflammation and autoimmunity. The disease is composed of an autoimmune component mediated by autoantibody immune complexes and B and T cell independent inflammation. The underlying mechanism is a gain-of-function mutation in Plcg2, which leads to hyperreactive external calcium entry in B cells and expansion of innate inflammatory cells. This mutant identifies Plcg2 as a key regulator in an autoimmune and inflammatory disease mediated by B cells and non-B, non-T haematopoietic cells and emphasizes that by distinct genetic modulation, a single point mutation can lead to a complex immunological phenotype. 相似文献
67.
Zusammenfassung Es wird über einen Fall akuter Erythroleukämie mit G-Trisomie berichtet und die mögliche Bedeutung hereditärer Faktoren für die Manifestation akuter Leukämien diskutiert.
Summary The cytogenetic analyses of direct bone marrow preparations in a 53 years old male with acute erythroleukaemia of 9 months disease history, revealed persistently a G-trisomy in a dominant cell line with 47 chromosomes. The peripheral blood culture preparations with phytohaemagglutinin exhibited normal diploid cell line.The frequent occurrence of akute leukaemia in Down's syndrome tempts to implicate that leukaemia with G-Trisomy having no signs of Down's syndrome is a somatic mutation initiated by some unknown hereditary recessive genes mechanisms.相似文献
68.
2-Bromoethoxycarbonyl modified amino acids were reacted with pyridine, 4-picoline and poly(4-vinylpyridine) to yield the corresponding 2-(N-pyridinio)ethoxycarbonyl derivatives as water-soluble amino-protecting groups. The kinetics and activation energies of basicly induced cleavage of the amino acids were investigated by 1H NMR spectroscopy in a D2O/NaOD medium. The polymeric salts were found to be more reactive than the low molecular weight pyridinium bromides because of electrostatic polymeric effects. Additionally, the kinetic measurements confirmed a E1cB mechanism for the cleavage of the urethane function. The formation of peptide bonds was performed in the case of poly[2-(N-4-vinylpyridinioethoxycarbonyl)]-protected amino acids in aqueous medium by water-soluble carbodiimides. 相似文献
69.
The present study focusses on the effects of ibuprofen and its enantiomers on cytokine production by peripheral blood monocytes and endothelial cells as well as on the potential modulation of ADM-expression by human umbilical vein endothelial cells and the concomitant effects on monocyte transendothelial migration as measured by a cell migration assay system. This consists of an endothelial cell monolayer on a solid collagen substrate, i.e. an artificial vessel wall construct. We observed a significant inhibition by 100 g/ml ibuprofen of VCAM-1 expression by endothelial cells while ELAM-1 and ICAM-1 expression was not influenced. However, we could not see any concomitant inhibitory effects on the spontaneous migration of monocytes after preincubating the endothelial cell monolayer with ibuprofen up to concentrations of 100 g/ml and activating with suboptimal and optimal concentrations of TNF-. Our monocyte transendothelial migration system reflects very sensitively endothelial cell-activation even by very low TNF- concentrations. (S)- and (R)-ibuprofen were equal in their inhibitory/activating effects on cytokine production, with the exception of stronger IL-8 induction in endothelial cells by (R)-ibuprofen as compared to its chiral analogue. 相似文献
70.
Phenotypic and genotypic analyses of enterohemorrhagic Escherichia coli O145 strains from patients in Germany 总被引:5,自引:0,他引:5
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Sonntag AK Prager R Bielaszewska M Zhang W Fruth A Tschäpe H Karch H 《Journal of clinical microbiology》2004,42(3):954-962
Enterohemorrhagic Escherichia coli (EHEC) strains of serogroup O145 are emerging as causes of diarrhea and the hemolytic-uremic syndrome. However, there have been few genetic analyses of this EHEC group. We investigated the serotypes, virulence genes, plasmid profiles, pulsed-field gel electrophoresis (PFGE) patterns, and genetic variability of the fliC and eae genes in 120 EHEC O145 strains isolated from cases of hemolytic-uremic syndrome (n = 24) or diarrhea (n = 96) in Germany between 1996 and 2002. Three isolates belonged to serotype O145:H28, one to serotype O145:H25, and 116 were nonmotile (O145:H(-)). One hundred fourteen of the nonmotile strains shared fliC restriction fragment length polymorphism (RFLP) patterns identical to that of the O145:H28 strains. The remaining two nonmotile strains displayed a fliC-RFLP pattern identical to that of the O145:H25 strain. Each of the 117 strains with the fliC-RFLP(H28) pattern harbored eae gamma, whereas the three strains with the fliC-RFLP(H25) pattern possessed eae beta. Five different stx genotypes, six combinations of plasmid-encoded putative virulence genes, 29 plasmid profiles, and 47 PFGE types were identified. Strains within some of the PFGE types could be further subtyped by means of distinct plasmid profiles. These data demonstrate that the EHEC O145 serogroup is comprised of two different serotypes that possess distinct eae types. The heterogeneity of EHEC O145 strains at the chromosomal and plasmid level, in particular the high diversity in PFGE patterns, provides a basis for molecular subtyping of these pathogens. 相似文献