Chiral Anomaly Effects and the BaBar Measurements of the γγ∗→π0\gamma\gamma^{*}\to \pi^{0} Transition Form Factor

The recent BaBar measurements of the $\gamma\gamma^{*}\to \pi^{0}$ transition form factor show spectacular deviation from perturbative QCD prediction for large space-like $Q^{2}$ up to $34\,\rm GeV^{2}$. When plotted against $Q^{2}$, $Q^{2}F(Q^{2})$ shows steady increase with $Q^{2}$ in contrast with the flat $Q^{2}$ behavior predicted by perturbative QCD, and at $34\,\rm GeV^{2}$ is more than 50% larger than the QCD prediction. Stimulated by the BaBar measurements, we revisit our previous paper on the cancellation of anomaly effects in high energy processes $Z^{0}\to \pi^{0}\gamma$, $e^{+}e^{-}\to \pi^{0}\gamma$ and apply our results to the $\gamma^{*}\gamma\to \pi^{0}$ transition form factor measured in the $e^{+}e^{-}\to e^{+}e^{-}\pi^{0}$ process with one highly virtual photon. We find that, the transition form factor $F(Q^{2})$ behaves as $(\frac{m^{2}}{Q^{2}})\times (\ln(Q^{2}/m^{2}))^{2}$ and produces a striking agreement with the BaBar data for $Q^{2}F(Q^{2})$ with $m=132\,\rm MeV$ which also reproduces very well the CLEO data at lower $Q^{2}$.Comment: v4, LaTeX, 8 pages, one figure, minor changes(references), to appear in Int. J. Mod. Phys.

Distinct subpopulations of enteric neuronal progenitors defined by time of development, sympathoadrenal lineage markers and Mash-1-dependence

Enteric and sympathetic neurons have previously been proposed to be lineally related. We present independent lines of evidence that suggest that enteric neurons arise from at least two lineages, only one of which expresses markers in common with sympathoadrenal cells. In the rat, sympathoadrenal markers are expressed, in the same order as in sympathetic neurons, by a subset of enteric neuronal precursors, which also transiently express tyrosine hydroxylase. If this precursor pool is eliminated in vitro by complement-mediated lysis, enteric neurons continue to develop; however, none of these are serotonergic. In the mouse, the Mash-1−/− mutation, which eliminates sympathetic neurons, also prevents the development of enteric serotonergic neurons. Other enteric neuronal populations, however, including those that contain calcitonin gene related peptide are present. Enteric tyrosine hydroxylase-containing cells co-express Mash-1 and are eliminated by the Mash-1−/− mutation, consistent with the idea that in the mouse, as in the rat, these precursors generate serotonergic neurons. Serotonergic neurons are generated early in development, while calcitonin gene related peptide-containing enteric neurons are generated much later. These data suggest that enteric neurons are derived from at least two progenitor lineages. One transiently expresses sympathoadrenal markers, is Mash-1-dependent, and generates early-born enteric neurons, some of which are serotonergic. The other is Mash-1-independent, does not express sympathoadrenal markers, and generates late-born enteric neurons, some of which contain calcitonin gene related peptide

Differential Role of “Signal 3” Inflammatory Cytokines in Regulating CD8 T Cell Expansion and Differentiation in vivo

Following an infection, naïve CD8 T cells are stimulated by dendritic cells (DC) displaying pathogen-derived peptides on MHC class I molecules (signal 1) and costimulatory molecules (signal 2). Additionally, pathogen-induced inflammatory cytokines also act directly on the responding CD8 T cells to regulate their expansion and differentiation. In particular, both type I interferons (IFNs) and IL-12 have been described as critical survival signals (signal 3) for optimal CD8 T cell accumulation during the expansion phase. Furthermore, expansion in numbers of antigen-specific CD8 T cells is coupled with their acquisition of effector functions to combat the infection. However, it still remains unclear whether these same cytokines also regulate the effector/memory differentiation program of the CD8 T cell response in vivo. Here, we demonstrate that defective signaling by either type I IFNs or IL-12 to the responding CD8 T cells impairs maximal expansion in response to DC immunization + CpG ODN, but neither of these cytokines is essential to regulate the effector/memory differentiation program. In addition, lack of direct IL-12 signaling to CD8 T cells accelerates the development of central memory phenotype in both primary and secondary antigen-specific memory CD8 T cells

Standardisation of Environmental Enrichment for Laboratory Mice and Rats: Utilisation, Practicality and Variation in Experimental Results

Rats and mice are the most commonly used species as laboratory animal models of diseases in biomedical  research. Environmental factors such as cage size, number of cage mates and cage structure such as environmental  enrichment can affect the physiology and behavioural development of laboratory animals and  their well-being throughout their lives. Therefore compromising the animals’ well-being due to inadequate  environmental conditions would diminish the value of the research models. In order to improve laboratory  animals’ well-being and promote the quality of animal based biomedical research, it is fundamentally  important that the environment of the animals meets the animals’ species typical behavioural needs. Standardisation  of environmental enrichment for laboratory rats and mice therefore should provide possibilities  for the animals to engage in at least the essential behavioural needs such as social contact, nest building,  exploring and foraging. There is a wide variety of environmental enrichment items commercially available  for laboratory mice and rats. However, how these items are used by the animals, their practicality in the  laboratory and whether these enrichments might lead to increased variation in experimental results have  not been widely assessed. In this study, we implemented two standardised enrichment items (shelters, nesting  materials) for rats and mice at different animal units. We instructed the animal care staff in monitoring  the use of enrichment items by the animals by means of a daily score sheet system. The animal staff ’s  viewpoint on practicality of the standardised enrichment program was assessed with a monthly score sheet  survey. Also we assessed whether the enriched environment affected breeding results and contributed to an  increase in variation of experimental data from several participating current studies. Our results show that  the animals readily used the provided enrichment items. A slight increase in workload for the animal staff  was reported. However, the overall judgement was mainly reported as good. Breeding results and variation  in experimental data did not reveal differences as compared to data from previous housing and/or non enriched  housing conditions. Overall, the results indicate that standard environmental enrichment that is species  appropriate may enhance the animal’s well-being without undesirable side effects on the experimental  outcome and daily working routine of the animal care staff.

К проблеме методологического статуса персонализированной медицины как практикоориентарованной учебной дисциплины

МЕДИЦИНСКИЕ УЧЕБНЫЕ ЗАВЕДЕНИЯОБРАЗОВАНИЕ МЕДИЦИНСКОЕСТУДЕНТЫУЧЕБНЫЕ ДИСЦИПЛИНЫПЕРСОНАЛИЗИРОВАННАЯ МЕДИЦИНАПРАКТИКО-ОРИЕНТИРОВАННАЯ ОБРАЗОВАТЕЛЬНАЯ СРЕДАПРАКТИКО-ОРИЕНТИРОВАННОЕ ОБУЧЕНИЕМЕТОДОЛОГИЧЕСКИЕ ПОДХОД

Coherence of Nitrogen-Vacancy Electronic Spin Ensembles in Diamond

We present an experimental and theoretical study of electronic spin decoherence in ensembles of nitrogen-vacancy (NV) color centers in bulk high-purity diamond at room temperature. Under appropriate conditions, we find ensemble NV spin coherence times (T_2) comparable to that of single NVs, with T_2 > 600 microseconds for a sample with natural abundance of 13C and paramagnetic impurity density ~10^15 cm^(-3). We also observe a sharp decrease of the coherence time with misalignment of the static magnetic field relative to the NV electronic spin axis, consistent with theoretical modeling of NV coupling to a 13C nuclear spin bath. The long coherence times and increased signal-to-noise provided by room-temperature NV ensembles will aid many applications of NV centers in precision magnetometry and quantum information.Comment: 5 pages, 3 figures; v2 minor correction