107 research outputs found

    Weak Gravity Conjecture in AdS/CFT

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    We study implications of the weak gravity conjecture in the AdS/CFT correspondence. Unlike in Minkowski spacetime, AdS spacetime has a physical length scale, so that the conjecture must be generalized with an additional parameter. We discuss possible generalizations and translate them into the language of dual CFTs, which take the form of inequalities involving the dimension and charge of an operator as well as the current and energy-momentum tensor central charges. We then test these inequalities against various CFTs to see if they are universally obeyed by all the CFTs. We find that certain CFTs, such as supersymmetric QCDs, do not satisfy them even in the large NN limit. This does not contradict the conjecture in AdS spacetime because the theories violating them are either unlikely or unclear to have weakly coupled gravitational descriptions, but it suggests that the CFT inequalities obtained here by naive translations do not apply beyond the regime in which weakly coupled gravitational descriptions are available.Comment: 9 pages, v2: references and comments adde

    Regulatory Role for Complement Receptors (CD21/CD35) in the Recombination Activating Gene Expression in Mouse Peripheral B Cells

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    A population of peripheral B cells have been shown to express recombination activating gene products, RAG-1 and RAG-2, which are considered to be involved in revising the B cell antigen receptor (BCR) in the periphery. BCR engagement has been reported to turn off RAG expression in peripheral B cells, whereas the same treatment has an opposite effect in immature B cells in the bone marrow. In contrast to receptor editing that is involved in the removal of autoreactivity in immature B cells, it has been shown that secondary V(D)J rearrangement in peripheral B cells, termed receptor revision, contributes to affinity maturation of antibodies. Here, we show that RAG-2 expression in murine splenic B cells was abrogated by the coligation of BCR with complement receptors (CD21/CD35) much more efficiently than by the engagement of BCR alone. On the other hand, the same coligation augmented proliferation of anti-CD40-stimulated B cells. Consistent with these observations, RAG-2 expression was lower in the draining lymph nodes of the quasi-monoclonal mice when they were immunized with a high-affinity antigen than with a low-affinity one. These findings suggest a crucial role for CD21/CD35 in directing the conservation or the revision of BCRs in peripheral B cells

    Weak gravity conjecture in the AdS/CFT correspondence

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    We study implications of the weak gravity conjecture in the AdS/CFT correspondence. Unlike in Minkowski spacetime, Anti-de Sitter (AdS) spacetime has a physical length scale, so that the conjecture must be generalized with an additional parameter. We discuss possible generalizations and translate them into the language of dual conformal field theories (CFTs), which take the form of inequalities involving the dimension and charge of an operator as well as the current and energy-momentum tensor central charges. We then test these inequalities against various CFTs to see if they are universally obeyed by all the CFTs. We find that certain CFTs, such as supersymmetric QCDs, do not satisfy them even in the large N limit. This does not contradict the conjecture in AdS spacetime because the theories violating them are either unlikely or unclear to have weakly coupled gravitational descriptions, but it suggests that the CFT inequalities obtained here by naive translations do not apply beyond the regime in which weakly coupled gravitational descriptions are available

    Weak gravity conjecture in the AdS/CFT correspondence

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    Regulatory Role for Complement Receptors (CD21/CD35) in the Recombination Activating Gene Expression in Mouse Peripheral B Cells

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    A population of peripheral B cells have been shown to express recombination activating gene products, RAG-l and RAG-2, which are considered to be involved in revising the B cell antigen receptor (BCR) in the periphery. BCR engagement has been reported to tum off RAG expression in peripheral B cells, whereas the same treatment has an opposite effect in immature B cells in the bone marrow. In contrast to receptor editing that is involved in the removal of autoreactivity in immature B cells, it has been shown that secondary V(D)J rearrangement in peripheral B cells, termed receptor revision, contributes to affinity maturation of antibodies. Here, we show that RAG-2 expression in murine splenic B cells was abrogated by the coligation of BeR with complement receptors (CD211CD35) much more efficiently than by the engagement of BCR alone. On the other hand, the same coligation augmented proliferation of anti-CD40-stimulated B cells. Consistent with these observations, RAG-2 expression was lower in the draining lymph nodes of the quasi-monoclonal mice when they were immunized with a high-affinity antigen than with a low-affinity one. These findings suggest a crucial role for CD211CD35 in directing the conservation or the revision of BCRs in peripheral B cells

    Geometric effects on critical behaviours of the Ising model

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    We investigate the critical behaviour of the two-dimensional Ising model defined on a curved surface with a constant negative curvature. Finite-size scaling analysis reveals that the critical exponents for the zero-field magnetic susceptibility and the correlation length deviate from those for the Ising lattice model on a flat plane. Furthermore, when reducing the effects of boundary spins, the values of the critical exponents tend to those derived from the mean field theory. These findings evidence that the underlying geometric character is responsible for the critical properties the Ising model when the lattice is embedded on negatively curved surfaces.Comment: 16 pages, 6 figures, to appear in J. Phys. A: Math. Ge

    Reconstruction of Insulin Signal Flow from Phosphoproteome and Metabolome Data

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    SummaryCellular homeostasis is regulated by signals through multiple molecular networks that include protein phosphorylation and metabolites. However, where and when the signal flows through a network and regulates homeostasis has not been explored. We have developed a reconstruction method for the signal flow based on time-course phosphoproteome and metabolome data, using multiple databases, and have applied it to acute action of insulin, an important hormone for metabolic homeostasis. An insulin signal flows through a network, through signaling pathways that involve 13 protein kinases, 26 phosphorylated metabolic enzymes, and 35 allosteric effectors, resulting in quantitative changes in 44 metabolites. Analysis of the network reveals that insulin induces phosphorylation and activation of liver-type phosphofructokinase 1, thereby controlling a key reaction in glycolysis. We thus provide a versatile method of reconstruction of signal flow through the network using phosphoproteome and metabolome data

    Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival

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    BACKGROUND: We assessed the nm23-H1 gene product expression and its relationship with lymphatic and blood vessel invasion in patients with esophageal squamous cell carcinoma. METHODS: Formalin-fixed and paraffin-embedded tissue sections from 45 patients who were treated surgically were used in this study. Pathologists graded lymphatic and blood vessel invasion in each of the tissue samples. Expression of nm23-Hl gene product was determined using a specific monoclonal antibody. RESULTS: Expression of nm23-H1 gene product was present in 17 (37.8%) cases. We found an inverse correlation between nm23-H1 gene product expression and lymphatic vessel invasion, whereas no correlation between nm23-H1 gene product expression and blood vessel invasion. Overall survival rate was not different between nm23-H1 gene product positive and negative patients (p = 0.21). However, reduced expression of nm23-H1 gene product was associated with shorter overall survival in patients with involved lymph nodes (p < 0.05), but not in patients without involved lymph nodes (p = 0.87). CONCLUSIONS: In patients with esophageal squamous cell carcinoma, there appears to be an inverse relationship between nm23-H1 gene product expression and lymphatic vessel invasion. Furthermore, nm23-H1 gene product expression might be a prognostic marker in patients with involved lymph nodes. Our data does not demonstrate any correlation between nm23-H1 gene product expression and blood vessel invasion
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