Dipolar spin correlations in classical pyrochlore magnets

We study spin correlations for the highly frustrated classical pyrochlore lattice antiferromagnets with O(N) symmetry in the limit T->0. We conjecture that a local constraint obeyed by the extensively degenerate ground states dictates a dipolar form for the asymptotic spin correlations, at all N $\ne$ 2 for which the system is paramagnetic down to T=0. We verify this conjecture in the cases N=1 and N=3 by simulations and to all orders in the 1/N expansion about the solvable N=infinity limit. Remarkably, the N=infinity formulae are an excellent fit, at all distances, to the correlators at N=3 and even at N=1. Thus we obtain a simple analytical expression also for the correlations of the equivalent models of spin ice and cubic water ice, I_h.Comment: 4 pages revtex

The modular S-matrix as order parameter for topological phase transitions

We study topological phase transitions in discrete gauge theories in two spatial dimensions induced by the formation of a Bose condensate. We analyse a general class of euclidean lattice actions for these theories which contain one coupling constant for each conjugacy class of the gauge group. To probe the phase structure we use a complete set of open and closed anyonic string operators. The open strings allow one to determine the particle content of the condensate, whereas the closed strings enable us to determine the matrix elements of the modular $S$-matrix, also in the broken phase. From the measured broken $S$-matrix we may read off the sectors that split or get identified in the broken phase, as well as the sectors that are confined. In this sense the modular $S$-matrix can be employed as a matrix valued non-local order parameter from which the low-energy effective theories that occur in different regions of parameter space can be fully determined. To verify our predictions we studied a non-abelian anyon model based on the quaternion group $H=\bar{D_2}$ of order eight by Monte Carlo simulation. We probe part of the phase diagram for the pure gauge theory and find a variety of phases with magnetic condensates leading to various forms of (partial) confinement in complete agreement with the algebraic breaking analysis. Also the order of various transitions is established.Comment: 37 page

Peroxisome Proliferator-Activated Receptors and Caloric Restriction-Common Pathways Affecting Metabolism, Health, and Longevity.

Caloric restriction (CR) is a traditional but scientifically verified approach to promoting health and increasing lifespan. CR exerts its effects through multiple molecular pathways that trigger major metabolic adaptations. It influences key nutrient and energy-sensing pathways including mammalian target of rapamycin, Sirtuin 1, AMP-activated protein kinase, and insulin signaling, ultimately resulting in reductions in basic metabolic rate, inflammation, and oxidative stress, as well as increased autophagy and mitochondrial efficiency. CR shares multiple overlapping pathways with peroxisome proliferator-activated receptors (PPARs), particularly in energy metabolism and inflammation. Consequently, several lines of evidence suggest that PPARs might be indispensable for beneficial outcomes related to CR. In this review, we present the available evidence for the interconnection between CR and PPARs, highlighting their shared pathways and analyzing their interaction. We also discuss the possible contributions of PPARs to the effects of CR on whole organism outcomes

Interplay between CCR7 and Notch1 axes promotes stemness in MMTV-PyMT mammary cancer cells

Background: Breast cancer is the major cause of cancer-related mortality in women. It is thought that quiescent stem-like cells within solid tumors are responsible for cancer maintenance, progression and eventual metastasis. We recently reported that the chemokine receptor CCR7, a multi-functional regulator of breast cancer, maintains the stem-like cell population. Methods: This study used a combination of molecular and cellular assays on primary mammary tumor cells from the MMTV-PyMT transgenic mouse with or without CCR7 to examine the signaling crosstalk between CCR7 and Notch pathways. Results: We show for the first time that CCR7 functionally intersects with the Notch signaling pathway to regulate mammary cancer stem-like cells. In this cell subpopulation, CCR7 stimulation activated the Notch signaling pathway, and deletion of CCR7 significantly reduced the levels of activated cleaved Notch1. Moreover, blocking Notch activity prevented specific ligand-induced signaling of CCR7 and augmentation of mammary cancer stem-like cell function. Conclusion: Crosstalk between CCR7 and Notch1 promotes stemness in mammary cancer cells and may ultimately potentiate mammary tumor progression. Therefore, dual targeting of both the CCR7 receptor and Notch1 signaling axes may be a potential therapeutic avenue to specifically inhibit the functions of breast cancer stem cells.Sarah T. Boyle, Krystyna A. Gieniec, Carly E. Gregor, Jessica W. Faulkner, Shaun R. McColl and Marina Kochetkov

Are there approximate relations among transverse momentum dependent distribution functions?

Certain exact relations among transverse momentum dependent parton distribution functions due to QCD equations of motion turn into approximate ones upon the neglect of pure twist-3 terms. On the basis of available data from HERMES we test the practical usefulness of one such ``Wandzura-Wilczek-type approximation'', namely of that connecting h_{1L}^{\perp(1)a}(x) to h_L^a(x), and discuss how it can be further tested by future CLAS and COMPASS data.Comment: 9 pages, 3 figure

Transverse momentum dependent distribution functions in a covariant parton model approach with quark orbital motion

Transverse parton momentum dependent distribution functions (TMDs) of the nucleon are studied in a covariant model, which describes the intrinsic motion of partons in terms of a covariant momentum distribution. The consistency of the approach is demonstrated, and model relations among TMDs are studied. As a byproduct it is shown how the approach allows to formulate the non-relativistic limit.Comment: 16 page

Autonomous bioluminescence imaging of single mammalian cells with the bacterial bioluminescence system.

Bioluminescence-based imaging of living cells has become an important tool in biological and medical research. However, many bioluminescence imaging applications are limited by the requirement of an externally provided luciferin substrate and the low bioluminescence signal which restricts the sensitivity and spatiotemporal resolution. The bacterial bioluminescence system is fully genetically encodable and hence produces autonomous bioluminescence without an external luciferin, but its brightness in cell types other than bacteria has, so far, not been sufficient for imaging single cells. We coexpressed codon-optimized forms of the bacterial luxCDABE and frp genes from multiple plasmids in different mammalian cell lines. Our approach produces high luminescence levels that are comparable to firefly luciferase, thus enabling autonomous bioluminescence microscopy of mammalian cells