Comparison of immunoglobulin heavy chain isotype expression in peyer's patch and splenic B-cells

Gayle E. Woloschak*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Past work has shown that B lymphocytes from Peyer's patches (PP) and from spleen differ from each other in the following ways: (1) PP are enriched for IgA-producing precursor cells while splenic B-cells are a rich source of IgM-precursor cells; and (2) PP are a poor source of antibody-secreting cells when compared to the spleen. The reasons for these differences are unclear. In this work B-cells have been examined expressing newly regenerated surface immunoglobulin heavy chains in murine PP and spleens for immunoglobulin isotype expression. Dual color immunofluorescence demonstrated higher levels of B-cells regenerating two surface isotypes in the PP (IgM+ IgG+ = 14.9%; IgM+ IgA+ = 9.4%) than in the spleen (IgM+ IgG+ = 0.4%; IgM+ IgA+ = 0.2%). Poly A+ RNA was purified from these B-cells and compared for immunoglobulin heavy chain isotype expression by DNA-excess slot blot hybridization. Splenic B-cells contained higher amounts (at least two-fold) of Ig heavy chain-specific mRNA per μg of polysomal RNA than did PP B-cells. Peyer's patches B-cells demonstrated slightly lower μ:α ratios than splenic B-cells. In vitro translation of the RNAs suggested higher levels of translatable α-specific Poly A+ RNA in PP B-cells than in B-cells from MLN or spleen; furthermore, splenic B-cell RNA contained higher levels of translatable μ-rna than did the other tissues examined. Northern blot analysis of RNA derived from these tissues identified major μ-, γ2b-, and α-hybridizing sequences, though PP-derived B-cell preparations were shown to be enriched for the membrane forms of mRNA for γ2b and α when compared to the spleen-derived B-cell preparations. These results suggest that the level of differentiation of PP B-cells (that are capable of regeneration of surface Ig) may differ significantly from that of splenic B-cells.

Original languageEnglish (US)
Pages (from-to)581-591
Number of pages11
JournalMolecular Immunology
Volume23
Issue number6
DOIs
StatePublished - Jun 1986

ASJC Scopus subject areas

  • Immunology
  • Molecular Biology

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