42 research outputs found

    Specific Expression of Human Intelectin-1 in Malignant Pleural Mesothelioma and Gastrointestinal Goblet Cells

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    Malignant pleural mesothelioma (MPM) is a fatal tumor. It is often hard to discriminate MPM from metastatic tumors of other types because currently, there are no reliable immunopathological markers for MPM. MPM is differentially diagnosed by some immunohistochemical tests on pathology specimens. In the present study, we investigated the expression of intelectin-1, a new mesothelioma marker, in normal tissues in the whole body and in many cancers, including MPM, by immunohistochemical analysis. We found that in normal tissues, human intelectin-1 was mainly secreted from gastrointestinal goblet cells along with mucus into the intestinal lumen, and it was also expressed, to a lesser extent, in mesothelial cells and urinary epithelial cells. Eighty-eight percent of epithelioid-type MPMs expressed intelectin-1, whereas sarcomatoid-type MPMs, biphasic MPMs, and poorly differentiated MPMs were rarely positive for intelectin-1. Intelectin-1 was not expressed in other cancers, except in mucus-producing adenocarcinoma. These results suggest that intelectin-1 is a better marker for epithelioid-type MPM than other mesothelioma markers because of its specificity and the simplicity of pathological assessment. Pleural intelectin-1 could be a useful diagnostic marker for MPM with applications in histopathological identification of MPM

    A compact synchroscan streak camera using a microchannel plate incorporated tube

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    A compact synchroscan streak camera, which incorporates a microchannel plates providing a high light gain, has been constructed. The camera has been operated in synchronism with a synchronous-passive hybrid mode-locked CW dye laser, and the overall time resolution has been 10.8 and 25.9 ps for a recording of ~160 and ~ lO^[8] cycles of dye laser pulses, respectively. In addition, by using the camera system with the dye laser a weak fluorescence profile (a quantum yield of ~10^[-3]) of an important biomolecule has been directly observed on a picosecond time scale

    群馬県の早植・普通期水稲栽培における育苗箱全量基肥栽培

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    Picosecond time-resolved fluorescence spectroscopy of hematoporphyrin derivative

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    The picosecond time-resolved fluorescence decays I(t) and spectra I(λ, t) for hematoporphyrin derivative (HPD) in a phosphate buffer saline aqueous solution at different concentrations (8.4 x 10^[-6] ~ 8.4 x 10^[-3] M) are measured by a two-dimensional synchroscan streak camera with a mode-locked CW dye laser, and a new emission band (which we call the Y-band) is found at high concentration. It is shown that the fluorescence decays composed of fast and slow components at high concentration are due to the Y-band (120 ps lifetime) from head-to-tail aggregates including equilibrium dimer and stable dimer, and the usual band (3.6 ns lifetime) from monomer, respectively, and the latter band is dynamically quenched by the Förster type resonance energy transfer from the monomer to the aggregate. Furthermore, the measurement of static fluorescence spectra from human gastric cancers and the surrounding in vivo after HPD injection shows that a band corresponding to the Y-band from the aggregate appears at only the cancerous cells

    Picosecond time-resolved fluorescence spectroscopy of hematoporphyrin derivative

    Get PDF
    The picosecond time-resolved fluorescence decays I(t) and spectra I(λ, t) for hematoporphyrin derivative (HPD) in a phosphate buffer saline aqueous solution at different concentrations (8.4 x 10^[-6] ~ 8.4 x 10^[-3] M) are measured by a two-dimensional synchroscan streak camera with a mode-locked CW dye laser, and a new emission band (which we call the Y-band) is found at high concentration. It is shown that the fluorescence decays composed of fast and slow components at high concentration are due to the Y-band (120 ps lifetime) from head-to-tail aggregates including equilibrium dimer and stable dimer, and the usual band (3.6 ns lifetime) from monomer, respectively, and the latter band is dynamically quenched by the Förster type resonance energy transfer from the monomer to the aggregate. Furthermore, the measurement of static fluorescence spectra from human gastric cancers and the surrounding in vivo after HPD injection shows that a band corresponding to the Y-band from the aggregate appears at only the cancerous cells
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