Biomedical subjects
K Moriguchi
Publications and source records attributed to K Moriguchi.
Complex carbohydrate histochemistry of the surface and gastric pit epitheliums of the Japanese macaque.
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Mucous cell types in the major and minor salivary glands of the Japanese macaque.
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Differentiation of human pulmonary alveolar epithelial cells revealed by peroxisome changes in pulmonary proteinosis.
Regenerating areas of human lungs in pulmonary fibrosis were observed electron microscopically, and peroxidatic activity of catalase in lung peroxisomes were demonstrated cytochemically. Proliferation of Type II cells was prominent there, and some of the cells extended their cytoplasms to cover the denuded basement membrane. Unusual intermediate cells between Type II and Type I cells were observed. The extension of cytoplasmic processes with new generation of pinocytotic vesicles strongly suggested a Type I cell profile. However, catalase-positive peroxisomes were found in these cells simultaneously. From these results it was concluded that Type I cells may originate from Type II cells in human lungs as they do in experimental animals.
[Action of steroid hormone in control of metabolism and its significance in initiation of pregnancy and gestation].
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Studies on fractionated irradiation. I. Response of mitotic cells in tumors to fractionated irradiation with different doses and intervals.
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Studies on fractionated irradiation. II. Effect of fractionation of irradiation with a constant dose and overall time on mitosis of Ehrlich tumor cells.
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Studies on fractionated irradiation. IV. Effect on suppression of mitosis of the interval between fractionated irradiation.
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Studies on fractionated irradiation. 3. Determination of the most effective interval between first and second treatments from the effect on mitosis of Ehrlich tumor cells.
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Cytochrome oxidase activity and confocal laser scanning microscopic analysis of the hamster submandibular gland using microwave irradiated fixation.
Submandibular glands of the hamster were irradiated in 2% paraformaldehyde (pFA)-0.5% pure glutaraldehyde (PGA) with a microwave (MW) processor at temperatures of 10 degrees and 37 degrees C. Electron microscopy showed that cytochrome oxidase activity was taking place in the mitochondrial intermembrane-intracristal space of the granular duct cell when the temperature of the MW-irradiated fixatives was at 10 degrees C. However, a decrease of this activity was observed when we took care to keep the temperature of the MW-irradiated fixatives at 37 degrees C. The distinct reduction of cytochrome oxidase activity allowed by MW irradiation seems to be due the thermal affects of fixatives. Of course, the possibility cannot be excluded that MW irradiation caused other undetectable membrane damage. Then, we used confocal laser scanning microscopy for the preservation check of the mitochondrial membrane for cytochemistry with MW-irradiated fixation. The fluorescence of rhodamine 123 was observed in the inner spaces of the mitochondria at temperatures of 10 degrees and 37 degrees C. When the same tissues were fixed with 2% pFA using an MW processor as the sole fixative at 10 degrees C, no mitochondrial fluorescence was observed. Cytochrome oxidase activity, by contrast, could be seen in the mitochondrial intermembrane-intracristal spaces in the same condition. Formaldehyde is not the best aldehyde for the purpose of ultrastructural preservation. On the other hand, light and electron microscopy showed that the endogenous peroxidase activity was localized in the nuclear envelope, endoplasmic reticulum, secretory granules, and Golgi apparatus of the hamster submandibular gland using 2% pFA-0.5% PGA fixative with and without MW irradiations at temperatures of 10 degrees and 37 degrees C. Some of the same cells were fixed with only 2% pFA under MW irradiation at 10 degrees C; however, marked diffuseness of the peroxidase activity was observed. Therefore, these results indicated that cytochrome oxidase activity was sensitive to heat with MW-irradiated fixation. Peroxidase activity was very resistant to heat with MW-irradiated fixation but not with pFA solo fixation, therefore, PGA had to be used.
Cytochemical detection of endogenous peroxidase in the acinar cells of the hamster submandibular gland.
The presence of endogenous peroxidase activity in the hamster submandibular gland was investigated cytochemically by light and electron microscopy using diaminobenzidine methods. After fixation of tissue with 2% paraformaldehyde-2.5% glutaraldehyde and incubation in a DAB reaction medium containing 0.01% H2O2, the peroxidase reaction product was localized in the nuclear envelope, the cisternae of the endoplasmic reticulum, secretory granules and the Golgi apparatus in both the acinar and granular duct cells of the submandibular gland. This is in contrast to earlier investigators who failed to detect peroxidase activity in acinar cells of the hamster submandibular gland and reported that peroxidase is localized only in the granular duct cells. The discrepancy may be caused by differences in experimental procedures. It is suggested that fixation of tissue with a high concentration of glutaraldehyde and incubation in a DAB reaction medium containing a high concentration of H2O2 inhibits the peroxidase activity of acinar cells in the hamster submandibular gland.
Increase of methionine-aminopeptidase activity in hyperplastic Leydig cells of rat cryptorchid testis.
In order to elucidate the reasons for the increased methionine-aminopeptidase activity in the rat cryptorchid testis, a histochemical study was conducted on the changes in testicular aminopeptidase activities using various substrates after the cryptorchidism experimentally was induced with reference to the regenerated hepatic cells which appeared in the partially hepatectomized liver of rat. Methionine-aminopeptidase gradually increased in Leydig cells after cryptorchid was induced, whereas the enzyme activity decreased in regenerated hepatic cells. These histochemical observations were coincident with the data obtained by enzyme assay. The present study has clearly indicated that the increased methionine aminopeptidase activity was specific for hyperplastic and hypertrophic Leydig cells in the cryptorchid testis, but did not depend merely on cell hyperplasia.