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  • Title: Efficient electric field-induced generation of hybridomas from human B lymphocytes without prior activation in vitro.
    Author: Kwekkeboom J, de Groot C, Tager JM.
    Journal: Hum Antibodies Hybridomas; 1992 Jan; 3(1):48-53. PubMed ID: 1576322.
    Abstract:
    In this study we investigated whether electrofusion would enable efficient hybridization of human B cells to occur without the need of prior activation in vitro. Two cell lines, the murine myeloma SP 2/0 and murine-human heteromyeloma F3B6, were used as fusion partners, and hybridization of human B cells purified either from peripheral blood or from solid lymphoid tissue (tonsil) was studied. Optimal hybridization frequencies were obtained at a poration field strength of 3 to 4 kV/cm. Electrofusion appeared to be a very efficient method to hybridize tonsillar B lymphocytes, resulting on the average in a hydridoma outgrowth of 1 per 1400 lymphocytes in fusions with SP 2/0 and 1 per 3300 in fusions with F3B6. Hybridization frequency in polyethylene glycol-induced fusions was only 1 per 13,000 tonsillar lymphocytes. Seventy-five percent of the resulting hybridomas secreted human immunoglobulin, either IgM or IgG. Electric field-induced hybridization of peripheral blood B lymphocytes resulted in immortalization of 1 per 17,500 lymphocytes when using Sp 2/0 as a fusion partner, and 1 per 15,000 with F3B6 as a fusion partner. Polyethylene glycol fusions yielded only 1 hybridoma per 160,000 blood lymphocytes. On average, 60% of the hybridomas obtained by fusing peripheral blood B cells secreted human immunoglobulin. Both IgM and IgG secretors were found. Furthermore, by the use of a fusion chamber with a small volume (35 microliters), hybridomas could be generated from small numbers (300,000 to 55,000) of human B cells. In conclusion, human B cells can be hybridized by electrofusion with myeloma cells with efficiencies comparable to those found for murine splenocytes, without the need for prior activation in vitro.
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