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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 72 (1986), S. 117-123 
    ISSN: 1432-0533
    Keywords: Ia antigen ; Cerebral macrophage ; Phagocytosis ; Perivascular cell ; Immunocytochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary As reported previously, the perivascular cells laden with fluorescent granules (FGP cell) are situated in Virchow-Robin space and show marked uptake capacity for intraventricularly administered substances. The phagocytic FGP cells are derived developmentally from leptomeningeal cells and are recognizable in various kinds of animals, including humans. In the present paper, the FGP cells of rodents are studied by immunological techniques. It is clearly demonstrated that rat FGP cells express the antigenic determinant for Ia antibody at about 7 days after birth, and also that mouse FGP cells show a positive reaction against mouse Fc and splenic macrophage antibodies at about the same developmental stage. The specific determinants of FGP cells appear concurrently with the initiation of horseradish peroxidase uptake. On the other hand, Ia antigen is also shown in subarachnoid macrophages, but not in immature FGP cells, endothelium and pericyte. Based on these findings, it seems reasonable to consider that the FGP cells are indigenous cerebral macrophages and significant for the local immune response in a cerebral tissue. Further, in this paper, to prevent confusion of the FGP cell with the other perivascular cells, the authors propose designating the FGP cell as Mato cell.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1617-4623
    Keywords: DNA repair ; DNA replication ; Homologous recombination ; Meiosis ; RecA gene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The mouseRad51 gene is a mammalian homologue of theEscherichia coli recA and yeastRAD51 genes, both of which are involved in homologous recombination and DNA repair in mitosis and meiosis. The expression of mouseRad51 mRNA was examined in synchronized mouse m5S cells. TheRad51 transcript was observed from late G1 phase through to M phase. During the period of late G1-S-G2, the RAD51 proteins were observed exclusively in nuclei. Activation by mitogens of T cell and B cell proliferation in spleen induced the expression ofRad51 mRNA. By immunohistochemical analyses, the mouse RAD51 protein was detected in proliferating cells: spermatogonia in testis, immature T cells in thymus, germinal center cells of the secondary lymphatic nodules of spleen and intestine, follicle cells in ovary and epithelial cells in uterus and intestine. It was also expressed in spermatocytes during early and mid-prophase of meiosis and in resting oocytes before maturation. Thus, mouseRad51 expression is closely related to the state of cell proliferation and is presumably involved in DNA repair coupled with DNA replication, as well as in meiotic DNA recombination in spermatocytes.
    Type of Medium: Electronic Resource
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