Pustular vasculitis with clinical feature of pustular psoriasis and sternoclavicular hyperostosis

We report the case of a 51-year-old Japanese man with a unique pustulosis. He had multiple erythematous plaques and numerous pinpoint pustules on the trunk and extremities resembling pustular psoriasis. Histologic features revealed a fully developed intraepidermal abscess filled with neutrophils and disrupted epidermal keratinocytes. Mild leukocytosclastic vasculitis was seen in the underlying dermis. A direct immunofluorescence study revealed IgM, Clq, C3 and fibrinogen deposits in the dermal vessels. The patient had also sternoclavicular hyperostosis. We think that this represents a unique type of pustular vasculitis distinct from pustular psoriasis.     

Characterization of an Exo-Maltotetraose-forming Amylase of Pseudomonas stutzeri and Application in p-Nitrophenyl β-D-Galactosyl-α-Maltooligosaccharides Production

Some kinetic characteristics and hydrolytic action patterns on various β-D -galactosyl-maltooligosaccharides (Gal-Gn), ranging in size from D.P. (degree of polymerization) 5 to 8, of an exo-maltotetraose-forming amylase of Pseudomonas stutzeri (G4-amylase) were examined to produce a few p-nitrophenyl β-D -galactosyl-α-maltooligosaccharides (Gal-GnP, n = 4,5). The relative hydrolytic reaction rates for larger Gal-Gn by the enzyme were larger than those for smaller saccharides tough the values for unmodified linear maltooligosachharides were almost same. Michaelis constants (Km) for hydrolysis of Gal-G4, Gal-G5, Gal-G6 and Gal-G7 by the enzyme were 1.3, 1.9, 1.3 and 1.3mM, and apparent molecular activities (ko) for these saccharides were 5.9, 38, 91 and 126s⁻¹, respectively. The values of ko/Km for them were remarkably smaller than those for unmodified linear maltooligosaccharides. The G4-amylase cleaved 2 points of the α-1,4-glucosidic linkage in β-1,4-Gal-G4 to give β-1,4-Gal-G2 and -Gal-G3 in the molar ratio of 3:1, whereas the enzyme attacked 3 points of the linkage in β-1,4-Gal-G5, -Gal-G6 and -Gal-G7 to form β-1,4-Gal-G2,-Gal-G3 and Gal-G4 in the molar ratios of 2:5:1, 1:3:6 and 1:3:6, in the early stage of the reaction, respectively. On the other hand, the enzyme showed no action on β-1,6-Gal-G4 and formed β-1,6-Gal-G4 solely from β-1,6-Gal-G5, and β-1,6-Gal-G4 and -Gal-G5 were from β-1,6-Gal-G6 and -Gal-G7 in the ratios of 8:1 and 2:1, respectively. The enzyme also catalyzed the transfer action to produce Gal-G3P, Gal-G4P and Gal-G5P, of which the formation ratio was coincided well with the hydrolytic action pattern on each Gal-Gn, from Gal-Gn tested as a donor and p-nitrophenyl α-glucoside (GP) as an acceptor in an aqueous solution containing 40% (v/v) methanol. By using this novel reaction, Gal-G5P is now producing on an industrial scale to apply as a substrate for the assay of human α-amylase.     

Photo-rechargeability of film electrodes prepared by pulsed laser deposition

The film electrodes of TiO₂, which have two functions of opto-electric conversion and storage of electrochemical energy, were prepared by pulsed laser deposition. To investigate the relationship between the photo-rechargeability and the surface structure, the TiO₂ film electrodes with different surface morphology were prepared by changing the inert gas pressure during the deposition. The photo-charged quantity was found to be proportional to the third power of the rms of surface roughness. The results suggest that not only the surface but also the interstices between crystal grains near the surface contribute to the photo-charging with low photo-emf.     

Color gamut mapping based on a perceptual image difference measure

Gamut mapping is a color transformation technique to solve a problem caused by mismatch of gamuts among imaging devices. One plausible goal of gamut mapping is to find a reproduction that is perceptually closest to the corresponding original image when an exact color matching is not possible. Several measures to quantify the perceptual difference between images have been proposed and applied to the gamut mapping problem. However most of the measures, such as average color difference, are applied on a pixel‐wise basis and show poor correlation with human visual perception. This article describes a model of the perceptual image difference for a given pair of images, which takes the human's contrast sensitivity into account and applies the model to a gamut mapping for generating a reproduction with minimum perceptual image difference. The model has a multispatial‐frequency channel structure with tunable peak gains for each channel, which are determined by psychophysical experiments, so that the model output fits the observer's sensitivity to the image difference. A gamut‐mapped image with minimum perceptual image difference is obtained by an iterative minimization process. To evaluate the proposed method, subjective evaluation experiments are performed to construct ratio scales that measure perceptual image difference of gamut‐mapped reproductions generated by the proposed and pixel‐wise methods. Results show that the reproductions by the proposed method are perceived as perceptually closest to the original, and the model's estimate of perceptual difference correlates better with the experimentally measured perceived image difference than other pixel‐wise measures. © 1999 John Wiley & Sons, Inc. Col Res Appl, 24, 280–291, 1999     

Analysis of the IgE-epitope of Der f 2, a major mite allergen, by in vitro mutagenesis

Der f 2 is a major mite allergen composed of 129 amino acid residues. To determine the major epitopes on Der f 2 recognized by human IgE antibodies, artificial mutations were introduced to Der f 2 protein. The IgE-binding activity of Der f 2 was significantly decreased by deletion of 10 amino acids at the N-terminus or nine amino acids at the C-terminus. Site-directed mutagenesis with a single amino acid replacement by Ala or Leu in both N- and C-terminal regions as well as a central portion was performed to generate 42 single-site mutations. Amino acid replacement around a disulfide bond of Cys8-Cys119 caused a marked decrease in IgE-binding activity. Furthermore, a distinct decrease in IgE-binding was also caused by Ala-substitution close to a disulfide bond of Cys73-Cys78 and by mutations of a few charged residues. From these results, it was concluded that the two disulfide-forming regions of Der f 2 and several charged residues are important for forming major epitope structures recognized by human IgE antibodies.     

Prostaglandin E receptor subtypes in mouse osteoblastic cell line

PGE2 is one of the key molecules in the osteoblast. It is the major prostanoid in the bone, and its production is under the control of both systemic and local factors. PGE2 has been reported to have multiple actions in the osteoblast, such as growth promotion and cell differentiation. To better understand the action of PGE2 in the osteoblast, we determined the PGE receptor subtypes in MC3T3-E1, an osteoblastic cell line derived from the normal mouse calvaria. Northern blot analysis revealed that EP1 and EP4 subtypes are expressed in MC3T3-E1. In contrast, EP3 subtype was not detected by either Northern blot analysis or RT-PCR. The contribution of each subtype was evaluated by studying the effects of subtype-specific analogs on osteoblastic function at confluency and 5 days after confluency. An EP1 agonist, 17-phenyl-omega-trinor PGE2, increased DNA synthesis and decreased alkaline phosphatase activity. 11-Deoxy-PGE1, and EP2 and EP4 agonist, decreased DNA synthesis and increased alkaline phosphatase activity at both stages. Butaprost, an EP2-selective agonist, showed effects similar to those of 11-deoxy-PGE1 only at confluency. Another and more differentiated osteoblastic marker, osteocalcin production, was detectable and was stimulated by 11-deoxy-PGE1 only 5 days after confluency. The exposure of these cells to EP1 agonist changed the cell shape to a more fibroblastic appearance. These results indicate that EP1, EP4, and probably EP2 are present in MC3T3-E1 cells; EP1 promotes cell growth, and EP2 and EP4 mediate differentiation of the osteoblast. Furthermore, the decreased response to EP2-specific agonist 5 days after confluency suggests that the expression of PGE receptor subtype is dependent on the stage of osteoblastic differentiation. This is the first report to determine PGE receptor subtypes in the bone.     

Anomalies of the tracheobronchial tree in patients with esophageal atresia

Bone marrow examination revealed a lipid-laden histiocytosis in seven patients undergoing long-term total parenteral nutrition necessitated by extensive short-bowel surgical resection. Clinical abnormalities occurred during this treatment which required bone marrow examination. These included hepatosplenomegaly and peripheral blood cytopenia; the median time to the detection of these abnormalities was 64 months. The most striking change within the bone marrow was the presence of many pigment-laden histiocytes which had the typical morphology of sea-blue histiocytes seen in the so-called idiopathic sea-blue histiocyte syndrome. The occurrence of sea-blue histiocytosis in the bone marrow in association with long-term parenteral nutrition for short-bowel syndrome has not, to our knowledge, been reported previously and should now be considered in the differential diagnosis of bone marrow sea-blue histiocytosis.     

Halo congenital nevus undergoing spontaneous regression. Involvement of T-cell immunity in involution and presence of circulating anti-nevus cell IgM antibodies

BACKGROUND: Halo congenital nevus is a condition in which halo formation is associated with congenital nevocellular nevi. Although several theories have been proposed, the immunologic mechanisms of halo formation and concomitant nevus regression still remain unclear. We presented immunologic findings in a case of halo congenital nevus with unique histologic location of inflammatory cells. OBSERVATIONS: Histologically, the present case of halo congenital nevus undergoing spontaneous regression showed a marked inflammatory infiltrate with remnants of original nevus cell nests. In the infiltrating T cells, CD8+ cells outnumbered CD4+ cells and the infiltrate of natural killer cells was not substantial. Direct and indirect immunofluorescence studies demonstrated the presence of IgM antibodies against nevus cells as well as melanoma cells and cultured melanocytes in the patient's serum. CONCLUSIONS: Our findings suggest that both T-cell-mediated immunity and IgM antibodies may be involved in the regression of halo congenital nevus. However, it is important to point out that our results may simply be epiphenomena and not directly responsible for the destruction of nevus cells.     

Terpendole E and its Derivative Inhibit STLC‐ and GSK‐1‐Resistant Eg5

Terpendole E is first natural product found to inhibit mitotic kinesin Eg5, but its inhibitory mechanism remains to be revealed. Here, we report the effects of terpendole E and 11ketopaspaline (a new natural terpendole E analogue) on the Eg5–microtubule interaction and in several Eg5 mutants. 11‐Ketopaspaline is a shunt product from terpendole E, and it shows potent inhibitory activity against the microtubule‐stimulated ATPase activity of Eg5. Unlike other Eg5 inhibitors, such as S‐trityl‐L ‐cysteine (STLC) and GSK‐1, both terpendole E and 11‐ketopaspaline only partially inhibited Eg5–microtubule interaction. Furthermore, terpendole E and 11‐ketopaspaline inhibited several Eg5 mutants that are resistant to STLC (Eg5^D130A, Eg5^L214A) or GSK‐1 (Eg5^I299F, Eg5^A356T), but with the same extent of inhibition against wild‐type Eg5. Because Eg5^D130A and Eg5^L214A show cross‐resistance to most known Eg5 inhibitors, which bind the L5 loop, these results suggest that terpendole E and its analogues have a different binding site and/or inhibitory mechanism to those for L5 loop‐binding type Eg5 inhibitors.