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M Sugimoto

Publications and source records attributed to M Sugimoto.

At least 505 records · Page 28Linked to original sources
PubMed1981

[A case of intracranial mesenchymal chondrosarcoma--changes observed by computed tomography before and after radiotherapy (author's transl)].

Intracranial mesenchymal chondrosarcoma is very rare, only 14 cases being reported in Europe and in the United States of America. Recently we experienced a case in which the follow-up indicating computed tomograms (CT) demonstrated interesting data on the radiosensitivity of this tumor. The patient, a 14-year-old female was admitted to out hospital with the complaint of left hemiplegia which had gradually progressed. CT revealed an area spreading upward from the right median base of the skull and consisted of two components showing (A) a density as high as that of calcium and (B) a density higher than that of surrounding brain tissue, but much lower than that of calcium. Temporoparietal craniotomy was performed to react approximately one-half of the tumor. Histological finding revealed mesenchymal chondrosarcoma. The component-A was though to be a cartilaginous tissue, and-B to be an undifferentiated mesenchymal tissue. Postoperative irradiation of 7,000 rad was initiated. The effect of radiotherapy as seen on computed tomograms is as follows, (1) decrease in the volume of the tumor by 26%, (2) decrease in density and enhancement of the area which is considered to be the undifferentiated mesenchymal cells, (3) mild reduction of the area which is considered to be the cartilaginous tissue, and (4) a very high density of the entire tumor similar in degree to that of the bone one year later. These results suggested that radiotherapy is effective for this tumor.

Adolescent↗
PubMed1981

Asymmetric division of lymphoid cells of the thymus of embryonic guinea-pigs. A cell kinetic study.

Cell division of thymus lymphoid cells from 30- to 60-day-old embryonic guinea-pigs, as well as young adults was investigated on cell smears stained with Giemsa. Asymmetrically dividing cells were found in the developmental stage of thymocytes. At the telophase of such cells, the cytoplasma of one of two immature daughter cells was apparently larger in amount than that of the counterpart cell. When 40-day embryonic lymphoid cells were examined, most of the asymmetrically dividing cells at telophase belonged to the larger cell population (mean diameter 15.7 micrometer). The mean diameters of the larger and smaller immature daughter cells of these dividing cells were estimated as 12.0 and 9.2 micrometer, respectively. Ultrastructural study also revealed a lymphoid cell which was under-going in situ apparent symmetric division at telophase. One of two immature daughter cells alone possessed a large cytoplasmic protrusion with few organella. The frequence of asymmetric division calculated by a rough estimation was around 10% of the total cell division between days 30 and 40 of embryonic development, and decreased thereafter. During this developmental period, thymic lymphoid cells were shown to progressively transform into smaller cells. A scheme regarding the mode of thymocyte proliferation during the embryonic period is proposed. and the biological meaning of the present phenomenon is discussed.

Animals↗
PubMed1980

Recognition of heterologous cells by macrophages. I. Species recognition by mouse and guinea pig macrophages in the phagocytosis of heterologous thymocytes.

The ability of macrophages to recognize homologous and various heterologous cells was studied in mice, rats, and guinea pigs, in terms of the in vitro phagocytosis of non-opsonized viable thymocytes by macrophages. Mouse, rat, and guinea pig macrophages were found to phagocytize actively thymocytes from certain heterologous animals, including chickens. For instance, mouse macrophages displayed conspicuous phagocytic activities against chicken and duck thymocytes, moderate activities against guinea pig and frog thymocytes and weak activities against rat and mouse thymocytes. On the other hand, guinea pig macrophages revealed a different behaviour: they ingested only chicken thymocytes. These observations strongly suggested that mammalian macrophages possess some ability to discriminate homologous from certain heterologous thymocytes. The results, however, did not necessarily support the idea that the degree of phagocytosis is simply related to the phylogenetic distance between the animal species from which thymocytes and macrophages originated, because of the apparent exception in the mode of phagocytosis by guinea pig macrophages. Evidence demonstrating that antibodies are not involved in this phenomenon will be presented in the accompanying paper.

Animals↗
PubMed1980

Recognition of heterologous cells by macrophages. II. The mechanism of phagocytosis of chicken thymocytes by mouse and guinea pig macrophages.

Mouse and guinea pig macrophages cultured in vitro actively phagocytize non-opsonized thymocytes from certain heterologous animals including chickens, as shown in the accompanying paper (11). The present study was undertaken to investigate the mechanism of this phenomenon, using the phagocytosis of chicken thymocytes (c-thymocytes) by mouse and guinea pig macrophages. The involvement in this phenomenon of natural IgG passively adsorbed in situ to macrophages was excluded, since the phagocytosis of c-thymocytes was not significantly affected by the treatment of macrophages with homologous IgG or rabbit anti-sera directed toward homologous IgG. The involvement of lectin- or sugar-like receptors seems also to be unlikely, since various glycoproteins showed no significant effect. c-Thymocytes treated with normal mouse serum (NMS) but not with heat-inactivated NMS were strongly stained with goat anti-mouse C3 by an indirect immunofluorescent technique, and became extremely vulnerable to adherence to and phagocytosis by mouse macrophages, suggesting that c-thymocytes are an activator of the alternative pathway of mouse complement. These results as a whole raise the possibility that mouse and guinea pig macrophages can phagocytize c-thymocytes by recognizing their activating surfaces of the alternative complement pathway without the participation of exogenously added IgG or complement, as proposed by others in the phagocytosis of rabbit and mouse red blood cells by human monocytes.

Animals↗