European Journal of Immunology · 1992 · 522 citations · 61 references
Life SciencesImmunologyPathologyDevelopmental ImmunologyImmunopathologyImmunoregulationB Cell BiologyB Cell DevelopmentB Cell RegulationCytokine BiologyHumoral ImmunityLymphocyte DevelopmentB Cell Cytokine RegulationB Cell-mediated ImmunityB Lymphocyte DevelopmentB-1 Cells
Previous work has shown that murine B lymphomas and purified normal peritoneal B cells produce interleukin‑10. The authors used a semi‑quantitative PCR assay to detect IL‑10 expression, finding it in peritoneal B cells and in splenic B cells of aged mice enriched for Ly‑1+ cells. IL‑10 production correlates with the presence of Ly‑1 (B‑1) B cells, is constitutively expressed in splenic B cells from Ly‑1+ BCL1 lymphoma mice, and suggests.
Abstract We have previously reported (O'Garra, A. et al., Int. Immunol. 1990. 2: 821) that murine B lymphomas and purified normal peritoneal B cells produce interleukin (IL) 10. We now show that this production of IL 10 B cells correlates with the presence of Ly‐1 (B‐1) B cells, in both normal and diseased mice. Using a semi‐quantitative modification of the polymerase chain reaction, we show that IL 10 expression is detectable in peritoneal B cells but only becomes apparent in splenic B cells of aged mice of which a high proportion are Ly‐1 + . Furthermore, the expression of IL 10 is constitutive in splenic B cells from mice carrying the Ly‐1 + BCL1 lymphoma. Since IL 10 is a potent regulator of in vitro immune function, its production by Ly‐1 lineage B (B‐1) cells raises the possibility that this subset of B cells may regulate their own development and/or the function of other immunocompetent cells.
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