Differential expression of SAP and EAT-2-binding leukocyte cell-surface molecules CD84, CD150 (SLAM), CD229 (Ly9) and

X Romero1, D Benítez, S March

  • 1Department of Cellular Biology and Pathology, Immunology Unit, Medical School, University of Barcelona and Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

Tissue Antigens
|July 13, 2004
PubMed

Insights

The CD150 (SLAM) family proteins, including CD84 and CD150, have wider expression on immune cells than previously known. Their differential distribution suggests unique roles in regulating adaptive and innate immune responses.

Area of Science:

  • Immunology
  • Cell Biology

Background:

  • The CD150 (SLAM) family comprises nine immunoglobulin superfamily proteins crucial for lymphocyte activation.
  • Six family members (CD84, CD150, CD229, CD244, NTB-A, CS1) associate with adapter proteins like SLAM-associated protein (SAP).
  • SAP mutations cause X-linked lymphoproliferative disease, highlighting the family's importance in immune function.

Purpose of the Study:

  • To investigate the expression patterns of CD84, CD150, CD229, and CD244 on various leukocyte and lymphocyte subsets.
  • To determine if these receptors are differentially expressed across hematopoietic cells.
  • To explore the potential non-redundant functions of these receptors in immune regulation.

Main Methods:

  • Flow cytometric analysis was employed to assess the expression of CD84, CD150, CD229, and CD244.
  • Expression levels were quantified on diverse leukocyte and lymphocyte populations, including thymocytes, T cells, antigen-presenting cells, monocytes, dendritic cells, and natural killer cells.

Main Results:

  • CD84 and CD150 were found on thymocytes, mature T cells, and antigen-presenting cells, with high expression on memory T cells.
  • CD150 expression increased significantly post-activation and was absent on resting monocytes and immature dendritic cells.
  • CD229 expression was limited to lymphocytes, while CD244 showed preferential expression on natural killer cells, CD8(+) effector cells, monocytes, basophils, and eosinophils.

Conclusions:

  • This study reveals a broader distribution of CD84, CD150, CD229, and CD244 than previously reported.
  • The differential expression of these receptors on hematopoietic cells suggests distinct, non-redundant roles.
  • These findings indicate that CD150 family members play significant roles in regulating both innate and adaptive immunity.

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