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Related Experiment Videos

Dependence of lymphocyte surface Ig on continuous polyclonal activation.

D M Bucholz, S Dray, M Teodorescu

    Immunology
    |August 1, 1979
    PubMed
    Summary

    Rabbit B lymphocytes shed and replace surface immunoglobulin (Ig) with a half-life of approximately 2 hours. This replacement, crucial for maintaining Ig levels, depends on continuous polyclonal activation, either external or internal.

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    Area of Science:

    • Immunology
    • Cell Biology
    • Molecular Biology

    Background:

    • Rabbit splenic B cells require continuous polyclonal stimulation to maintain surface immunoglobulin (Ig).
    • Without stimulation, B cells shed surface Ig but do not replace it, leading to loss.

    Purpose of the Study:

    • To investigate the mechanism behind the loss or maintenance of surface Ig on rabbit B cells.
    • To determine if mitogen stimulation affects surface Ig by preventing shedding or promoting resynthesis.

    Main Methods:

    • Cultured rabbit splenic B cells with and without mitogens (B-cell specific: SM, LPS; T-cell specific: Con A, PHA).
    • Used inhibitors of mRNA and protein synthesis to assess the role of resynthesis.
    • Labeled surface Ig with 125I-labelled Fab anti-allotype antibody to track turnover.

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  • Cultured cells under crowded conditions to investigate endogenous factors.
  • Main Results:

    • Inhibitors of mRNA and protein synthesis abolished mitogen-induced Ig maintenance, indicating resynthesis is required.
    • Mitogen stimulation led to surface Ig turnover (shedding and replacement) with a half-life of ~2 hours.
    • B-cell mitogens maintained surface Ig, while T-cell mitogens did not, suggesting direct B-cell activation is necessary.
    • Crowded conditions induced a macroglobulin-associated factor that maintained surface Ig turnover, mimicking polyclonal activation.

    Conclusions:

    • Rabbit B lymphocytes shed and replace surface Ig with a half-life of approximately 2 hours.
    • Surface Ig replacement, not shedding, is dependent on continuous exogenous or endogenous polyclonal activation.
    • Direct B-cell stimulation is essential for maintaining surface Ig levels.