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Complement-dependent B-cell activation by cobra venom factor and other mitogens?

P Dukor, G Schumann, R H Gisler

    The Journal of Experimental Medicine
    |February 1, 1974
    PubMed
    Summary
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    Cobra venom factor activates both T and B lymphocytes, acting as a T-cell substitute for antibody formation. This potent inducer highlights the crucial role of complement C3 in B-cell activation and proliferation.

    Area of Science:

    • Immunology
    • Complement System
    • Cell Signaling

    Background:

    • B-cell activation requires two signals: antigen/mitogen binding and activated complement C3 interaction.
    • B-cell mitogens and T-independent antigens activate the complement system's alternative pathway.
    • The role of complement C3 in B-cell activation warrants further investigation.

    Purpose of the Study:

    • To investigate the effect of cobra venom factor (CVF) on B-cell activation.
    • To elucidate the role of complement C3 in B-cell responses.
    • To determine if CVF can substitute for T cells in antibody formation.

    Main Methods:

    • Administered purified cobra venom factor to mouse lymphocytes (T and B cells).
    • Assessed antibody formation in B-cell cultures supplemented with macrophages or 2-mercaptoethanol.

    Related Experiment Videos

  • Investigated the effect of CVF and serum on B-cell rosette formation and mitogen reactivity.
  • Main Results:

    • Cobra venom factor demonstrated mitogenic activity for both T and B lymphocytes.
    • CVF substituted for T cells, restoring antibody formation in B-cell cultures.
    • B-cell proliferation induced by mitogens and CVF depended on the availability of exogenous C3.

    Conclusions:

    • Cobra venom factor is a potent inducer of B-cell activation, potentially by providing activated C3.
    • Complement C3 is essential for T-cell-dependent and T-cell-independent B-cell activation and proliferation.
    • CVF can serve as a valuable tool for studying B-cell activation pathways and the complement system.