Effects of Acoustic Context on the Perceptual Differences between Spatial Sound Stimuli

We studied the effects of the acoustic context on active and passive discrimination of moving sound signals. Different contexts were created by reversing the role of standard and deviant stimuli in the oddball blocks, while their acoustical features were kept the same. Three types of sounds were used as standard or deviant stimuli in different blocks: stationary midline noises and two (smooth and abrupt) moving sounds moving to the left or right of the midline. Auditory event-related potentials (ERPs) were recorded during passive listening (the sound stimulation ignored), and mismatch negativity potentials (MMNs) were obtained. Active discrimination of sound movements was measured by the hit rate (percent correct responses) and false alarm rate, as well as the reaction time. The influence of the stimulus context on active and passive discrimination of the moving sound stimuli was reflected in the phenomenon known as the effect of deviance direction. The hit rate and MMN amplitude were higher when the deviant moved faster than the standard. The MMN amplitude was more responsive to the velocity of sound stimuli than the hit rate and false alarm rate. The psychophysical measurements in the reversed contexts suggest that smooth and abrupt sound movements may belong to the same perceptual category (moving sounds), while the stationary stimuli form another perceptual category.     

Demonstration of microtubules in the terminal web of mature absorptive cells from the small intestine of the rat

Summary The terminal web (TW) region of mature absorptive cells in the small intestine of the rat contains an elaborate cytoskeleton which supports the apical microvillus membrane. In studies regarding the structural organization of the cytoskeleton and associated proteins in the small intestine, microtubules have not been mentioned as components of the TW. By transmission electron microscopy of conventional resin-embedded sections of rat small intestine, we observe many microtubule profiles in the TW of mature absorptive cells. These microtubules are found in various orientations, although most course parallel to the long axis of the cell, and many microtubule profiles are seen in close association with smooth-surfaced vesicles.     

Detection of HLA-DR associated PLT determinants by alloreactive lymphocyte clones

This study deals with alloreactive T-cell clones which recognize cellular determinants associated with HLA-DR antigens. Two clones, CB55 and DS56, exhibited a PLT specificity that was perfectly associated with DR5. On the other hand, clones CB7, DS1 and HS1 showed PLT reactivity with approximately one-half of the DR5 positive cells and none of the DR5 negative cells, whereas clone MD4 largely reacted with the other half of DR5 positive cells. Another MLR culture generated two alloreactive clones DS6 and DS9 with PLT specificity for DR2. However, these clones did not respond to DR2 cells, which were also positive for the DR2-associated HLA-B7 and B18 antigens. Monoclonal antibody (mAb) inhibition studies showed heterogenous patterns, whereby monomorphic non-DR mAbs inhibited the DR2-associated PLT clones while the DR5-associated PLT clones were inhibited by different groups of anti-DR and non-DR mAbs. These observations suggest the existence of several lymphocyte-activating determinants associated with HLA-DR antigens. This diversity may be an important consideration in studies of the role of HLA-DR in immune mechanisms and transplant compatibility.     

Host Factors Determine Anti-GM1 Response Following Oral Challenge of Chickens with Guillain-Barré Syndrome Derived Campylobacter jejuni Strain GB11

Background

Anti-ganglioside antibodies with a pathogenic potential are present in C. jejuni-associated Guillain-Barré syndrome (GBS) patients and are probably induced by molecular mimicry. Immunization studies in rabbits and mice have demonstrated that these anti-ganglioside antibodies can be induced using purified lipo-oligosaccharides (LOS) from C. jejuni in a strong adjuvant.

Methodology/Principal Findings

To investigate whether natural colonization of chickens with a ganglioside-mimicking C. jejuni strain induces an anti-ganglioside response, and to investigate the diversity in anti-ganglioside response between and within genetically different chicken lines, we orally challenged chickens with different C. jejuni strains. Oral challenge of chickens with a C. jejuni strain from a GBS patient, containing a LOS that mimics ganglioside GM1, induced specific IgM and IgG anti-LOS and anti-GM1 antibodies. Inoculation of chickens with the Penner HS:3 serostrain, without a GM1-like structure, induced anti-LOS but no anti-ganglioside antibodies. We observed different patterns of anti-LOS/ganglioside response between and within the five strains of chickens.

Conclusions

Natural infection of chickens with C. jejuni induces anti-ganglioside antibodies. The production of antibodies is governed by both microbial and host factors.     

Activation of CMV promoter-controlled glycosyltransferase and β -galactosidase glycogenes by butyrate, tricostatin A, and 5-Aza-2′-deoxycytidine

Cytomegalovirus (CMV) immediate early promoter is a powerful promoter frequently used for driving the expression of transgenes in mammalian cells. However, this promoter gradually becomes silenced in stably transfected cells. We employed Chinese Hamster Ovary (CHO) and human pancreatic cancer (Panc 1) cells stably tansfected with three glycogenes driven by a CMV promoter to study the activation of silenced glycogenes. We found that butyrate, tricostatin A (TSA), and 5-aza-2-deoxycytidine (5-Aza-dC) can activate these CMV-driven glycogenes. The increase in mRNA and protein of a glycogene occurred 8–10 h after butyrate treatment, suggesting an indirect effect of butyrate in the activation of the transgene. The enhanced expression of the trangenes by butyrate and TSA, known inhibitors of histone deacetylase, was independent of the transgene or cell type. However, the transgene can be activated by these two agents in only a fraction of the cells derived from a single clone, suggesting that inactivation of histone deacetylase can only partially explain silencing of the transgenes. Combination treatment of one or both agents with 5-Aza-dC, a known inhibitor of DNA methylase, resulted in a synergistic activation of the transgene, suggesting a cross-talk between histone acetylation and DNA demethylation. Understanding the mechanisms of the inactivation and reactivation of CMV promoter-controlled transgenes should help develop an effective strategy to fully activate the CMV promoter-controlled therapeutic genes silenced by the host cells. Published in 2005.     

Initial experience with treatment of human B cell lymphoma with anti-CD19 monoclonal antibody

Summary Six patients with progressive B cell non-Hodgkin's lymphoma have been treated with an IgG2a mouse monoclonal antibody (mAb) against the B cell differentiation antigen CD19, with total doses varying from 225 mg to 1000 mg. Free mAb was detected in the serum after doses of 15–30 mg. After the mAb infusions the number of circulating tumour cells was temporarily reduced, but in some cases antibody-coated cells remained in the circulation for several days. mAb penetrated to extravascular tumour sites; in general higher doses were required to saturate cells in the lymph nodes than to sensitize tumour cells in the bone marrow. mAb doses of up to 250 mg were given i.v. over 4 h without major toxicity. One patient twice achieved a partial remission after two periods of mAb treatment with an 8-month interval; the second remission lasted for 9 months. One patient showed a minor response. None of the patients made antibodies against the mouse immunoglobulin. Serum immunoglobulin levels were followed as a measure of the function of the normal B cell compartment; no significant changes were seen up to 6 months after mAb treatment.Supported by the Dutch Cancer Society (grant NKI 84-14)     

Cytogenetic analysis of three genetic sexing strains of Ceratitits capitata

Summary Polytene chromosomes of three genetic sexing strains of Ceratitis capitata were analyzed. The genetic sexing mechanism is based on a pupal color dimorphism (white-brown) and is the result of a reciprocal translocation between the Y chromosome and the autosome bearing the w locus (white pupal case). The analyzed polytene chromosomes were derived from two different pupal tissues, the orbital bristle and fat body cells. The Y chromosome is visible in both tissues, while the autosomes present a different banding pattern. Based on these features, the autosome breakpoints in the three Y; autosome translocations were mapped, and the homology of the translocated autosome in both tissues was established. In addition, the location of the break-points was compared to the stability of these three strains.     

Development of a screening relationship to describe migration of contaminant vapors into buildings

The relationship between subsurface contaminant concentrations and indoor air concentrations, arising from the migration of contaminant vapors into buildings, is affected by a number of complex processes and parameters, many of which are subject to uncertainty. A study was undertaken to develop a simplified relationship between subsurface contaminant concentrations and indoor air concentrations. This relationship is intended for use as a screening tool to determine the relative significance of vapor transport and inhalation as an exposure scenario in the establishment of soil quality guidelines. The relationship was developed using a proprietary model to analyze the infiltration of subsurface vapors into buildings. A probabilistic analysis of the relationship, using a form of Monte Carlo simulation, was undertaken to estimate the dilution of contaminant concentrations between the source (soil gas) and point of exposure (indoor air). Using standardized values for certain parameters and generic distributions for key variables, probability distributions were generated for the dilution factor as a function of contaminant depth and soil type.     

An analysis of molecular polymorphism of esterase M produced by motileAeromonas strains

The high levels of electrophoretic polymorphism of esterase M detected in eight distinct hybridization groups of motileAeromonas raise questions of genetic homogeneity of the electromorphs. The 40 electromorphs detected fall in fourM _r classes—75, 80, 90, and 110 kD—and one typical variant belonging to each of these classes was purified. The four purified esterases exhibited the same resistance to heat, topH and to diisopropyl fluorophosphate, the sameK _m values for 1-naphthyl acetate and 1-naphthyl propionate (1mm), and immunological cross-reactions. Within each class, the electromorphs appeared to be related in term of single amino acid substitutions as estimated from their comparative titration patterns. The titration curves of the four purified esterases were strictly parallel suggesting close structural similarities. Thus, despite considerable variation in theirpI,M _F,andM _r values, it seems likely that the variants of esterase M are the products of closely related loci originating from a common ancestral gene.This work was supported by a grant from the Conseil Scientifique de la Faculté Xavier Bichat (Université Paris VII).