Reversible expression of CD138 on mature follicular B cells is downregulated by IL-4

Immunol Lett. 2013 Nov-Dec;156(1-2):38-45. doi: 10.1016/j.imlet.2013.09.004. Epub 2013 Sep 9.

Abstract

CD138, known as a marker of plasma cells, was reported to be expressed to an intermediate level in the murine bone marrow precursor B cells. Here an intermediate level of CD138 expression was also noted in a subpopulation of splenic follicular B cells, which were distinguishable from CD138(high) plasma cells, whereas the majority of transitional or marginal zone B cells did not express CD138. These CD138(int) B cells were IgM(low)IgD(high) mature B cells, located within follicular B cell zone, and expressed a lower level of CD21 than CD138(-) follicular B cells. During in vitro culture of splenic cells, the proportion of CD138(int) B cells increased, which was noticeably reversed by the addition of IL-4 to the culture. The experiments with sorted CD138(int) cells showed that IL-4-mediated regulation of the CD138 expression was B cell-intrinsic and independent of in vitro B cell death. Our results demonstrate that mouse CD138(int) B cells characterize a subpopulation of IgM(low)IgD(high) mature follicular B cells. The CD138 expression on follicular B cells may represent a reversible status, reflecting a dynamic state probably influenced by IL-4.

Keywords: CD138; FO B cells; Follicular B cell; IL-4; MZ B cells; NKT cells; PNA; STAT6; Syndecan-1; T helper type 2 cells; Th2 cells; follicular B cells; interleukin-4; marginal zone B cells; natural killer T cells; peanut agglutinin; signal transducer and activator of transcription 6.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD19 / immunology
  • Antigens, CD19 / metabolism
  • Antigens, CD1d / immunology
  • Antigens, CD1d / metabolism
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocyte Subsets / metabolism
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • CD5 Antigens / immunology
  • CD5 Antigens / metabolism
  • Cells, Cultured
  • Down-Regulation / drug effects
  • Down-Regulation / immunology*
  • Flow Cytometry
  • Immunoglobulin D / immunology
  • Immunoglobulin D / metabolism
  • Immunoglobulin M / immunology
  • Immunoglobulin M / metabolism
  • Interleukin-4 / immunology*
  • Interleukin-4 / pharmacology
  • Leukosialin / immunology
  • Leukosialin / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Microscopy, Fluorescence
  • Plasma Cells / immunology
  • Plasma Cells / metabolism
  • Receptors, Complement 3d / immunology
  • Receptors, Complement 3d / metabolism
  • Spleen / cytology
  • Spleen / immunology
  • Spleen / metabolism
  • Syndecan-1 / immunology*
  • Syndecan-1 / metabolism

Substances

  • Antigens, CD19
  • Antigens, CD1d
  • CD5 Antigens
  • Immunoglobulin D
  • Immunoglobulin M
  • Leukosialin
  • Receptors, Complement 3d
  • Sdc1 protein, mouse
  • Syndecan-1
  • Interleukin-4