40 research outputs found
Superconformal symmetry and maximal supergravity in various dimensions
In this paper we explore the relation between conformal superalgebras with 64
supercharges and maximal supergravity theories in three, four and six
dimensions using twistorial oscillator techniques. The massless fields of N=8
supergravity in four dimensions were shown to fit into a CPT-self-conjugate
doubleton supermultiplet of the conformal superalgebra SU(2,2|8) a long time
ago. We show that the fields of maximal supergravity in three dimensions can
similarly be fitted into the super singleton multiplet of the conformal
superalgebra OSp(16|4,R), which is related to the doubleton supermultiplet of
SU(2,2|8) by dimensional reduction. Moreover, we construct the ultra-short
supermultiplet of the six-dimensional conformal superalgebra OSp(8*|8) and show
that its component fields can be organized in an on-shell superfield. The
ultra-short OSp(8*|8) multiplet reduces to the doubleton supermultiplet of
SU(2,2|8) upon dimensional reduction. We discuss the possibility of a chiral
maximal (4,0) six-dimensional supergravity theory with USp(8) R-symmetry that
reduces to maximal supergravity in four dimensions and is different from
six-dimensional (2,2) maximal supergravity, whose fields cannot be fitted into
a unitary supermultiplet of a simple conformal superalgebra. Such an
interacting theory would be the gravitational analog of the (2,0) theory.Comment: 54 pages, PDFLaTeX, Section 5 and several references added. Version
accepted for publication in JHE
AdS Field Theory from Conformal Field Theory
We provide necessary and sufficient conditions for a Conformal Field Theory
to have a description in terms of a perturbative Effective Field Theory in AdS.
The first two conditions are well-known: the existence of a perturbative `1/N'
expansion and an approximate Fock space of states generated by a finite number
of low-dimension operators. We add a third condition, that the Mellin
amplitudes of the CFT correlators must be well-approximated by functions that
are bounded by a polynomial at infinity in Mellin space, or in other words,
that the Mellin amplitudes have an effective theory-type expansion. We explain
the relationship between our conditions and unitarity, and provide an analogy
with scattering amplitudes that becomes exact in the flat space limit of AdS.
The analysis also yields a simple connection between conformal blocks and AdS
diagrams, providing a new calculational tool very much in the spirit of the
S-Matrix program.
We also begin to explore the potential pathologies associated with higher
spin fields in AdS by generalizing Weinberg's soft theorems to AdS/CFT. The AdS
analog of Weinberg's argument constrains the interactions of conserved currents
in CFTs, but there are potential loopholes that are unavailable to theories of
massless higher spin particles in flat spacetime.Comment: 31+7 pages, 5 figure
Bounds on 4D Conformal and Superconformal Field Theories
We derive general bounds on operator dimensions, central charges, and OPE
coefficients in 4D conformal and N=1 superconformal field theories. In any CFT
containing a scalar primary phi of dimension d we show that crossing symmetry
of implies a completely general lower bound on the central
charge c >= f_c(d). Similarly, in CFTs containing a complex scalar charged
under global symmetries, we bound a combination of symmetry current two-point
function coefficients tau^{IJ} and flavor charges. We extend these bounds to
N=1 superconformal theories by deriving the superconformal block expansions for
four-point functions of a chiral superfield Phi and its conjugate. In this case
we derive bounds on the OPE coefficients of scalar operators appearing in the
Phi x Phi* OPE, and show that there is an upper bound on the dimension of Phi*
Phi when dim(Phi) is close to 1. We also present even more stringent bounds on
c and tau^{IJ}. In supersymmetric gauge theories believed to flow to
superconformal fixed points one can use anomaly matching to explicitly check
whether these bounds are satisfied.Comment: 47 pages, 9 figures; V2: small corrections and clarification
Quantum Symmetries and Marginal Deformations
We study the symmetries of the N=1 exactly marginal deformations of N=4 Super
Yang-Mills theory. For generic values of the parameters, these deformations are
known to break the SU(3) part of the R-symmetry group down to a discrete
subgroup. However, a closer look from the perspective of quantum groups reveals
that the Lagrangian is in fact invariant under a certain Hopf algebra which is
a non-standard quantum deformation of the algebra of functions on SU(3). Our
discussion is motivated by the desire to better understand why these theories
have significant differences from N=4 SYM regarding the planar integrability
(or rather lack thereof) of the spin chains encoding their spectrum. However,
our construction works at the level of the classical Lagrangian, without
relying on the language of spin chains. Our approach might eventually provide a
better understanding of the finiteness properties of these theories as well as
help in the construction of their AdS/CFT duals.Comment: 1+40 pages. v2: minor clarifications and references added. v3: Added
an appendix, fixed minor typo
Successful radiation treatment of anaplastic thyroid carcinoma metastatic to the right cardiac atrium and ventricle in a pacemaker-dependent patient
Anaplastic thyroid carcinoma (ATC) is a rare, aggressive malignancy, which is known to metastasize to the heart. We report a case of a patient with ATC with metastatic involvement of the pacemaker leads within the right atrium and right ventricle. The patient survived external beam radiation treatment to his heart, with a radiographic response to treatment. Cardiac metastases are usually reported on autopsy; to our knowledge, this is the first report of the successful treatment of cardiac metastases encasing the leads of a pacemaker, and of cardiac metastases from ATCs, with a review of the pertinent literature
The Actin Associated Protein Palladin Is Important for the Early Smooth Muscle Cell Differentiation
Palladin, an actin associated protein, plays a significant role in regulating cell adhesion and cell motility. Palladin is important for development, as knockdown in mice is embryonic lethal, yet its role in the development of the vasculature is unknown. We have shown that palladin is essential for the expression of smooth muscle cells (SMC) marker genes and force development in response to agonist stimulation in palladin deficient SMCs. The goal of the study was to determine the molecular mechanisms underlying palladin's ability to regulate the expression of SMC marker genes. Results showed that palladin expression was rapidly induced in an A404 cell line upon retinoic acid (RA) induced differentiation. Suppression of palladin expression with siRNAs inhibited the expression of RA induced SMC differentiation genes, SM α-actin (SMA) and SM22, whereas over-expression of palladin induced SMC gene expression. Chromatin immunoprecipitation assays provided evidence that palladin bound to SMC genes, whereas co-immunoprecipitation assays also showed binding of palladin to myocardin related transcription factors (MRTFs). Endogenous palladin was imaged in the nucleus, increased with leptomycin treatment and the carboxyl-termini of palladin co-localized with MRTFs in the nucleus. Results support a model wherein palladin contributes to SMC differentiation through regulation of CArG-SRF-MRTF dependent transcription of SMC marker genes and as previously published, also through actin dynamics. Finally, in E11.5 palladin null mouse embryos, the expression of SMA and SM22 mRNA and protein is decreased in the vessel wall. Taken together, our findings suggest that palladin plays a key role in the differentiation of SMCs in the developing vasculature
Glucose Transporter 1 and Monocarboxylate Transporters 1, 2, and 4 Localization within the Glial Cells of Shark Blood-Brain-Barriers
Although previous studies showed that glucose is used to support the metabolic activity of the cartilaginous fish brain, the distribution and expression levels of glucose transporter (GLUT) isoforms remained undetermined. Optic/ultrastructural immunohistochemistry approaches were used to determine the expression of GLUT1 in the glial blood-brain barrier (gBBB). GLUT1 was observed solely in glial cells; it was primarily located in end-feet processes of the gBBB. Western blot analysis showed a protein with a molecular mass of 50 kDa, and partial sequencing confirmed GLUT1 identity. Similar approaches were used to demonstrate increased GLUT1 polarization to both apical and basolateral membranes in choroid plexus epithelial cells. To explore monocarboxylate transporter (MCT) involvement in shark brain metabolism, the expression of MCTs was analyzed. MCT1, 2 and 4 were expressed in endothelial cells; however, only MCT1 and MCT4 were present in glial cells. In neurons, MCT2 was localized at the cell membrane whereas MCT1 was detected within mitochondria. Previous studies demonstrated that hypoxia modified GLUT and MCT expression in mammalian brain cells, which was mediated by the transcription factor, hypoxia inducible factor-1. Similarly, we observed that hypoxia modified MCT1 cellular distribution and MCT4 expression in shark telencephalic area and brain stem, confirming the role of these transporters in hypoxia adaptation. Finally, using three-dimensional ultrastructural microscopy, the interaction between glial end-feet and leaky blood vessels of shark brain was assessed in the present study. These data suggested that the brains of shark may take up glucose from blood using a different mechanism than that used by mammalian brains, which may induce astrocyte-neuron lactate shuttling and metabolic coupling as observed in mammalian brain. Our data suggested that the structural conditions and expression patterns of GLUT1, MCT1, MCT2 and MCT4 in shark brain may establish the molecular foundation of metabolic coupling between glia and neurons