Mediators from cloned T helper cell lines affect immunoglobulin expression by B cells.

Publisher Website
Google Scholar
Abstract
When cloned [mouse] T helper cells encounter antigen presented by I-A-compatible macrophages, soluble mediators are produced that affect the differentiation and activation of normal B lymphocytes and cell lines of the B lineage. Exposure to such T cell culture supernatants causes 2 effects in the murine 70Z/3 cell line, which represents a pre-B stage of differentiation. These cells begin to synthesize Ig L chains and gain membrane Ig that is detectable by immunofluorescence. Two other effects are seen after similar treatment of the WEHI-279.1 murine cell line, which represents a mature, Ig+ B cell. These cells shift the ratio of .mu. chains produced from mostly membrane to mostly secretory type and begin to secrete large amounts of IgM, which can be detected either by biosynthetic radiolabeling followed by immunoprecipitation or by a staphylococcal protein A plaque assay. The majority also die. Similar to WEHI-279.1, normal small resting B cells also show the shift from membrane .mu. to secretory .mu. and are activated to Ig secretion after exposure to these supernatants. Products from T cell immune reactions apparently exert multiple effects on B cell development and activation, at several stages of the B cell developmental pathway. The observed changes range from nuclear processes, including gene transcription and RNA splicing, to such post-translational aspects as protein processing, catabolism, membrane architecture and cell survival.