Chikayoshi Oura
Kumamoto University
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Featured researches published by Chikayoshi Oura.
Cell and Tissue Research | 1992
Kiyotaka Toshimori; Ichiro Tanii; Shukuro Araki; Chikayoshi Oura
SummaryMN9, a monoclonal antibody raised against mouse spermatozoa, specifically recognizes the equatorial segment of sperm head in several mammalian species, including humans. Colloidal gold-immuno-electron microscopy of mouse spermatozoa has shown that the antigen is localized in the space between the outer and inner acrosome membranes and on the acrosome membranes at the equatorial segment. Immunoblotting after electrophoresis of spermatozoa from the cauda epididymidis has identified two immunoreactive bands: 38 kDa and 48 kDa in mouse, and 48 kDa in rat. During spermiogenesis in rat, this antigen is transported to the equatorial segment via a unique pathway, first appearing in some cisternae of the endoplasmic reticulum and in the Golgi apparatus of spermatids at around step 3. The antigen can further be found on the vesicles at thetrans-side of the Golgi apparatus, in the matrix of the head cap, and on the head cap membrane in step-4 to step-7 spermatids. The antigen appears to be concentrated at the equatorial segment during late spermiogenesis. Neither the (pro-)acrosomic granule nor the surrounding membrane are required in this pathway. This pathway can be termed the ‘Golgi-head cap tract’.
Journal of Hand Surgery (European Volume) | 1991
Dean O. Smith; Chikayoshi Oura; Chihiro Kimura; Kiyotaka Toshimori
An exhaustive anatomic dissection of all of the veins of the finger distal to the proximal interphalangeal joint was done. More than 3200 segments of veins were individually dissected out, measured, and recorded. From this survey new schematic diagrams have been drawn emphasizing the pertinent venous anatomy at the proximal, distal interphalangeal joints and eponychial levels. Suggestions are made for regions that are apt to have the largest vessels available for anastomosis.
Journal of Hand Surgery (European Volume) | 1991
Dean O. Smith; Chikayoshi Oura; Chihiro Kimura; Kiyotaka Toshimori
The arterial architecture in the finger distal to the proximal interphalangeal joint was studied in sixty-seven cadaver fingers with the aid of an operating microscope. The course, frequency, location, and diameter of the dorsal nail fold artery and its anastomosis was recorded. Similar measurements were performed for the palmar anastomosis. The frequency of arterial tortuosity in the digital artery was compiled and a classification of its morphology devised. The characteristic of arterial tortuosity provides a degree of protection to these essential structures. Failure to recognize this facet of arterial anatomy may be one more factor contributing to our inability to successfully revascularize the distal finger in certain patients.
Cell and Tissue Research | 1992
Ichiro Tanii; Kiyotaka Toshimori; Shukuro Araki; Chikayoshi Oura
SummaryA monoclonal antibody (MC41) was produced that specifically recognizes a sperm acrosomal antigen of approximately 165000 dalton in the rat. Rat testis was examined using a pre-embedding immunoperoxidase technique to reveal the pathway of the MC41 antigen to the acrosome during spermiogenesis. The MC41 immunoreaction appeared in several organelles of spermatids in a stage-specific manner: (1) in the endoplasmic reticulum (ER) throughout spermiogenesis, (2) in the outer acrosomal membrane from steps 9 to 19, (3) as a weak immunoreaction in the vesicular structures in the acrosomal matrix from steps 11 to 17, and (4) as a strong immunoreaction in the acrosomal matrix especially at the terminal step of spermiogenesis (step 19). However, no immunoreaction was observed in the Golgi region throughout spermiogenesis. These results suggest that the pathway of the MC41 antigen leads firstly from the ER to the outer acrosomal membrane and secondly to the acrosomal matrix. This pathway does not involve the Golgi apparatus and is referred to as the “extra-Golgi pathway”.
Archives of Andrology | 1991
Kiyotaka Toshimori; Shukuro Araki; Chikayoshi Oura; Edward M. Eddy
Using a monoclonal antibody T21, we reported that a mouse sperm maturation-associated antigen sialoglycoprotein of 54000 daltons (54K sialoglycoprotein) was secreted at the distal caput to proximal corpus epididymidis and that the 54K sialoglycoprotein had a hidden determinant (cryptodeterminant), which could be eliminated by sialidase treatment (Toshimori et al. (1988): Histochemistry 90:195-200; (1990a): Biol Reprod 42:151-160; (1990b): Arch Histol Cytol 53:339-349). This study evaluated the mouse sperm susceptibility to phagocytosis by macrophage in vitro. Comparisons were made between sperm from the caput epididymidis (caput sperm) incubated in modified Krebs Ringers solution (MKR) and caput sperm incubated in MKR containing cauda fluid, and between sialylated (sialidase-untreated) sperm from the corpus and cauda epididymidis (corpus/cauda sperm) and desialylated (sialidase-treated) corpus/cauda sperm. The results showed that macrophages were least actively engaged in phagocytosis for caput sperm incubated in MKR containing cauda fluid, and most active for desialylated corpus/cauda sperm. Incubation of caput sperm in MKR containing cauda fluid revealed that the 54K sialoglycoprotein in cauda fluid could be bound to the flagellar surface of caput sperm. These results together with previous findings strongly suggest that the 54K sialoglycoprotein bound to immature sperm during maturation in the epididymis is implicated in the protection of sperm from phagocytosis with the aid of sialic acid residues.
Cell and Tissue Research | 1990
Hirotaka Toshimori; Kiyotaka Toshimori; Naoto Minamino; Kenji Kangawa; Chikayoshi Oura; Shigeru Matsukura; Hisayuki Matsuo
SummaryAn immunohistochemical study using antiserum raised against synthetic chicken natriuretic polypeptide was used to investigate the distribution of this peptide in the chicken heart. Immunoreactive cells, both in the atrial and ventricular walls, were identified by electron microscopy, and electron-dense granules in the atrial and ventricular cardiocytes were revealed to be storage sites of the peptide. The electron-dense material, thought to be the peptide, was found in the sarcoplasmic reticulum, and it is suggested that a secretory pathway of the peptide through the latter to extracellular space, may be present, in addition to an exocytotic one.
American Journal of Anatomy | 1985
Kiyotaka Toshimori; Higashi R; Chikayoshi Oura
Histochemistry and Cell Biology | 1988
Kiyotaka Toshimori; Shukuro Araki; Chikayoshi Oura
Biology of Reproduction | 1990
Kiyotaka Toshimori; Sanae Araki; Chikayoshi Oura
Molecular Reproduction and Development | 1991
Kiyotaka Toshimori; Ichiro Tanii; Chikayoshi Oura; Edward M. Eddy