Inhibition of neutrophil migration by a selective inhibitor of matrix metalloproteinase: analysis by intravital microscopy

Observation of the microcirculation of the hamster cheek pouch by intravital microscopy revealed five steps of neutrophil migration from the venules after topical application of leukotriene B4 to the microvasculature: rolling along the venular wall (Step 1), adhesion to it (Step 2), disappearance from the vascular lumen (Step 3), presence between the endothelial cells and the subendothelial basement membrane (Step 4) and passage through the basement membrane (Step 5). The present study was performed to examine whether a metalloproteinase inhibitor inhibits neutrophil migration at any of the above five steps. Chymostatin and leupeptin did not inhibit any of these five steps. In contrast, FN-439, a selective inhibitor of matrix metalloproteinase, reduced the number of neutrophils in the perivascular space without affecting Steps 1 to 3. It was concluded that neutrophils may use metalloproteinase (collagenase/gelatinase) to penetrate the subendothelial basement membrane

Finite Higgs mass without Supersymmetry

We identify a class of chiral models where the one-loop effective potential for Higgs scalar fields is finite without any requirement of supersymmetry. It corresponds to the case where the Higgs fields are identified with the components of a gauge field along compactified extra dimensions. We present a six dimensional model with gauge group U(3)xU(3) and quarks and leptons accomodated in fundamental and bi-fundamental representations. The model can be embedded in a D-brane configuration of type I string theory and, upon compactification on a T^2/Z_2 orbifold, it gives rise to the standard model with two Higgs doublets.Comment: 28 pages, 4 figures, uses axodraw. Some typos corrected and references rearrange

Study of nuclear correlation effects via 12C(p,n)12N(g.s.,1+) at 296 MeV

We report measurements of the cross section and a complete set of polarization observables for the Gamow--Teller ${}^{12}{\rm C}(\vec{p},\vec{n}){}^{12}{\rm N}({\rm g.s.},1^+)$ reaction at a bombarding energy of 296 MeV. The data are compared with distorted wave impulse approximation calculations employing transition form factors normalized to reproduce the observed beta-decay $ft$ value. The cross section is significantly under-predicted by the calculations at momentum transfers $q \gtrsim$ 0.5 ${\rm fm^{-1}}$. The discrepancy is partly resolved by considering the non-locality of the nuclear mean field. However, the calculations still under-predict the cross section at large momentum transfers of $q$ $\simeq$ 1.6 ${\rm fm^{-1}}$. We also performed calculations employing random phase approximation response functions and found that the observed enhancement can be attributed in part to pionic correlations in nuclei.Comment: 5 figures, submitted to Phys. Lett.

Extranatural Inflation

We present a new model of inflation in which the inflaton is the extra component of a gauge field in a 5d theory compactified on a circle. The chief merit of this model is that the potential comes only from non-local effects so that its flatness is not spoiled by higher dimensional operators or quantum gravity corrections. The model predicts a red spectrum (n ~ 0.96) and a significant production of gravitational waves (r ~ 0.11). We also comment on the relevance of this idea to quintessence.Comment: 4 pages. Minor corrections and references added. Accepted for PR

Complete set of polarization transfer coefficients for the 3He(p,n){}^{3}{\rm He}(p,n) reaction at 346 MeV and 0 degrees

We report measurements of the cross-section and a complete set of polarization transfer coefficients for the ${}^{3}{\rm He}(p,n)$ reaction at a bombarding energy $T_p$ = 346 MeV and a reaction angle $\theta_{\rm lab}$ = $0^{\circ}$. The data are compared with the corresponding free nucleon-nucleon values on the basis of the predominance of quasi-elastic scattering processes. Significant discrepancies have been observed in the polarization transfer $D_{LL}(0^{\circ})$, which are presumably the result of the three-proton $T$ = 3/2 resonance. The spin--parity of the resonance is estimated to be $1/2^-$, and the distribution is consistent with previous results obtained for the same reaction at $T_p$ = 48.8 MeV.Comment: 4 figures, Accepted for publication in Physical Review

Biocompatibility of cross-linked hyaluronate (Gel-200) for the treatment of knee osteoarthritis

SummaryObjectiveTo compare the biocompatibility and immunogenicity of two intra-articular hyaluronan formulations, Gel-200 (Gel-One®) and hylan G-F 20 (Synvisc® series).Experimental designA comparison of the biocompatibility of Gel-200 and hylan G-F 20 was made using a rat subcutaneous air pouch model and the knee joint of normal rabbits. Immunogenicity was evaluated using a homologous passive cutaneous anaphylaxis (PCA) assay in guinea pigs.ResultsIn the air pouch model in rats, characteristic fibrous belts formed in the subcutaneous tissue. Injection of hylan G-F 20 into the air pouch induced granulomatous nodules primarily composed of macrophages, multinucleated giant cells, and eosinophils accompanied with the test material in the center of the nodules in the fibrous belt. Furthermore, the thickness of the fibrous belt in the hylan G-F 20 group increased significantly compared to the saline group. Injection of Gel-200 into the air pouch induced neither granulomatous inflammation nor significant thickening of fibrous belt, while foamy macrophages containing the test material were observed. Intra-articular injection of hylan G-F 20 into the rabbit knee joints induced granulomatous inflammation, eosinophil infiltration, and significant increase in the number of cells in the synovial fluid, while these findings were absent in the Gel-200 group. In the immunogenicity assay, hylan G-F 20 induced a positive PCA reaction, but the Gel-200 did not.ConclusionGel-200 showed more favorable biocompatibility and less immunogenicity compared to hylan G-F 20. Gel-200 is expected to be a single injection hyaluronan product with less safety concerns for the treatment of knee osteoarthritis (OA) pain