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    Comparison of haemopoiesis in young and old mice.

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    Authors
    Schofield, Raymond
    Dexter, T Michael
    Lord, Brian I
    Testa, Nydia G
    Affiliation
    Paterson Laboratories, Christie Hospital and Holt Radium Institute, Wilmslow Road, Manchester M20 9BX, UK.
    Issue Date
    1986-03
    
    Metadata
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    Abstract
    Haemopoietic status and functions have been compared in young (2-3-month-old) and old (2-2.5-year-old) BDF1 mice. The parameters measured include total marrow cellularity, CFU-S, CFU-mix, GM-CFC, BFU-E and CFU-F. In all cases the numbers of these cells in the femoral marrow of the old mice was equal to or greater than those in the femoral marrow of young mice. In addition to these parameters we have compared the ability of marrow from young and old mice to repopulate the marrow of recipient mice whose marrow had been eliminated by radiation; to grow in long-term bone marrow cultures; to produce ectopic grafts of marrow beneath the renal capsule of normal recipients; and to supply inhibitor and stimulator of stem cell proliferation in the marrow and to resynthesise these substances. We could detect no differences in any of these functions with the exception of that of resynthesis of the stem cell regulator substances, which appears to be somewhat slower in the old mice. This, however, does not impose any limitation upon the ability of the marrow to function either under normal conditions or in conditions requiring rapid proliferation. Therefore we can find no evidence whatsoever to suggest that aging of the haemopoietic system plays any part in aging of the individual or influencing the life-span.
    Citation
    Comparison of haemopoiesis in young and old mice. 1986, 34 (1):1-12 Mech Ageing Dev
    Journal
    Mechanisms of Ageing and Development
    URI
    http://hdl.handle.net/10541/116837
    DOI
    10.1016/0047-6374(86)90100-4
    PubMed ID
    3520172
    Type
    Article
    Language
    en
    ISSN
    0047-6374
    ae974a485f413a2113503eed53cd6c53
    10.1016/0047-6374(86)90100-4
    Scopus Count
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    All Paterson Institute for Cancer Research

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