Immunosurveillance of lung melanoma metastasis in EBI-3-deficient mice mediated by CD8+ T cells.

EBV-induced gene 3 (EBI-3) codes for a soluble type I receptor homologous to the p40 subunit of IL-12 that is expressed by APCs following activation. In this study, we assessed the role of EBI-3 in a model of lung melanoma metastasis. Intravenous injection of the B16-F10 cell line resulted in a significant reduction of lung tumor metastasis in EBI-3(-/-) recipient mice compared with wild-type mice. The immunological finding accompanying this effect was the expansion of a newly described cell subset called IFN-gamma producing killer dendritic cells associated with CD8(+) T cell responses in the lung of EBI-3(-/-) mice including IFN-gamma release and TNF-alpha-induced programmed tumor cell death. Depletion of CD8(+) T cells as well as targeting T-bet abrogated the protective effects of EBI-3 deficiency on lung melanoma metastases. Finally, adoptive transfer of EBI-3(-/-) CD8(+) T cells into tumor bearing wild-type mice inhibited lung metastasis in recipient mice. Taken together, these data demonstrate that targeting EBI-3 leads to a T-bet-mediated antitumor CD8(+) T cell responses in the lung

Convergence of energy-dependent incommensurate antiferromagnetic neutron scattering peaks to commensurate resonance in underdoped bilayer cuprates

The recently discovered coexistence of incommensurate antiferromagnetic neutron scattering peaks and commensurate resonance in underdoped YBa$_2$Cu$_3$O$_{6+x}$ is calling for an explanation. Within the t-J model, the doping and energy dependence of the spin dynamics of the underdoped bilayer cuprates in the normal state is studied based on the fermion-spin theory by considering the bilayer interactions. Incommensurate peaks are found at $[(1\pm\delta)\pi,\pi]$ and $[\pi,(1\pm\delta)\pi]$ at low energies with $\delta$ initially increasing with doping at low dopings and then saturating at higher dopings. These incommensurate peaks are suppressed, and the parameter $\delta$ is reduced with increasing energy. Eventually it converges to the $[\pi,\pi]$ resonance peak. Thus the recently observed coexistence is interpreted in terms of bilayer interactions.Comment: 15 pages, Revtex, five figures are included, accepted for publication in Phys. Rev.

Spin Susceptibility in Underdoped YBa2Cu3O6+x\bf YBa_2Cu_3O_{6+x}

We report a comprehensive polarized and unpolarized neutron scattering study of the evolution of the dynamical spin susceptibility with temperature and doping in three underdoped single crystals of the \YBCO{6+x} high temperature superconductor: \YBCO{6.5} (Tc = 52 K), \YBCO{6.7} (Tc = 67 K), and \YBCO{6.85} (T_c = 87 K). Theoretical implications of these data are discussed, and a critique of recent attempts to relate the spin excitations to the thermodynamics of high temperature superconductors is given.Comment: minor revisions, to appear in PR

Spin dynamics of stripes

The spin dynamics of stripes in high-temperature superconductors and related compounds is studied in the framework of a spin-wave theory for a simple spin-only model. The magnon dispersion relation and the magnetic structure factor are calculated for diagonal and vertical stripes. Acoustical as well as optical bands are included in the analysis. The incommensurability and the $\pi$ resonance appear as complementary features of the band structure at different energy scales. The dependence of spin-wave velocities and resonance frequencies on the stripe spacing and coupling is calculated. At low doping, the resonance frequency is found to scale roughly inversely proportional to the stripe spacing. The favorable comparison of the results with experimental data suggests that the spin-only model provides a suitable and simple basis for calculating and understanding the spin dynamics of stripes.Comment: 11 page, 10 figures, pdf version with high-res.pics at http://www.thp.uni-koeln.de/~sts

Differences in the pattern and regulation of mineral deposition in human cell lines of osteogenic and non-osteogenic origin

Bone marrow-derived mesenchymal stem cells (MSCs) are widely used as a cellular model of bone formation, and can mineralize in vitro in response to osteogenic medium (OM). It is unclear, however, whether this property is specific to cells of mesenchymal origin. We analysed the OM response in 3 non-osteogenic lines, HEK293, HeLa and NTera, compared to MSCs. Whereas HEK293 cells failed to respond to OM conditions, the 2 carcinoma-derived lines NTera and HeLa deposited a calcium phosphate mineral comparable to that present in MSC cultures. However, unlike MSCs, HeLa and NTera cultures did so in the absence of dexamethasone. This discrepancy was confirmed, as bone morphogenetic protein inhibition obliterated the OM response in MSCs but not in HeLa or NTera, indicating that these 2 models can deposit mineral through a mechanism independent of established dexamethasone or bone morphogenetic protein signalling