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Blimp-1 overcomes the block in IgM secretion in lipopolysaccharide/anti- mu F(ab') sub(2)-co-stimulated B lymphocytes
Ist Teil von
European journal of immunology, 1996-01, Vol.26 (1), p.268-271
Erscheinungsjahr
1996
Quelle
Wiley Online Library
Beschreibungen/Notizen
A combination of signals transmitted through the antigen receptor, membrane-bound cell interaction molecules and cytokine receptors induces B cell proliferation and differentiation into immunoglobulin-secreting or memory cells. It has recently been suggested by Turner et al. (Cell 1994. 77: 297) that the complex changes in gene activities accompanying high levels of immunoglobulin secretion are under the common control of a master regulator, Blimp-1 (B lymphocyte-induced maturation protein). We show here that in naive mouse B cells stimulated with lipopolysaccharide (LPS) alone (which leads to high IgM production), Blimp-1 is highly expressed, while cells co-stimulated with LPS and anti- mu F(ab') sub(2) show low levels of Blimp-1 mRNA and no longer secrete Ig. I gamma 1 sterile transcripts are, however, up-regulated after receptor co-ligation. Addition of interleukin (IL)-2 and IL-5 to LPS + anti- mu F(ab') sub(2)-treated primary B cells led to up-regulation of Blimp-1 and IgM secretion. Transfection of a Blimp-1 expression vector also induced IgM secretion. The data indicate that Blimp-1 is an important regulator of immunoglobulin secretion by primary B cells, and suggest that its level of expression may determine the differentiation to Ig-secreting plasma cells or entrance and maintenance in the memory pool.
Sprache
Englisch
Identifikatoren
ISSN: 0014-2980
Titel-ID: cdi_proquest_miscellaneous_15616045
Format
–
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