Identification and characterization of the low-affinity receptor for immunoglobulin E (FcepsilonRII/CD23) on murine

Yuzuru Nagaoka1, Koichiro Nakamura, Nami Yasaka

  • 1Department of Dermatology, Faculty of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8655, Japan. NAGAOKA-DER@h.u-tokyo.ac.jp

Insights

Murine cultured Langerhans cells express CD23, a receptor for immunoglobulin E (IgE). This finding contradicts previous studies and suggests CD23

Area of Science:

  • Immunology
  • Cell Biology
  • Dermatology

Background:

  • CD23, a low-affinity IgE receptor, is expressed on various hemopoietic cells.
  • Human epidermal Langerhans cells express CD23, but its presence on murine Langerhans cells remains unconfirmed.
  • Previous studies have failed to identify CD23 on murine Langerhans cells.

Purpose of the Study:

  • To investigate the expression of CD23 on murine Langerhans cells.
  • To reconcile conflicting previous findings regarding CD23 expression in murine Langerhans cells.
  • To explore the functional implications of CD23 expression in murine Langerhans cells.

Main Methods:

  • Isolation of highly enriched murine epidermal Langerhans cells (>95%) using the panning method.
  • Analysis of CD23 expression via fluorescence-activated cell sorter (FACS) analysis and polymerase chain reaction (PCR).
  • Investigation of IgE binding to cultured Langerhans cells and inhibition studies using anti-CD23 monoclonal antibody.

Main Results:

  • CD23 was detected on cultured murine Langerhans cells but not on freshly isolated cells.
  • PCR analysis confirmed CD23 DNA sequences in cultured Langerhans cells, identical to spleen leukocytes.
  • Culturing with keratinocyte-derived cytokines downregulated CD23 expression; IgE binding was observed and partially inhibited by anti-CD23 antibody.

Conclusions:

  • Murine cultured Langerhans cells express CD23, resolving previous discrepancies potentially due to cytokine influence.
  • The expression of CD23 on murine Langerhans cells suggests a role in IgE-mediated immune responses.
  • This study provides evidence for CD23's involvement in IgE binding and immune modulation in murine skin.

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