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Human blood basophils display a unique phenotype including activation linked membrane structures
C Stain1, H Stockinger, M Scharf
1I. Medical Department, University of Vienna, Austria.
Blood
|December 1, 1987
Summary
Human basophils share myeloid markers but express unique activation structures like IL-2 receptors. These findings suggest basophils may represent an activated cell population with distinct surface determinant profiles.
Area of Science:
- Immunology
- Cell Biology
- Hematology
Background:
- Basophils are a type of granulocyte with complex roles in immune responses.
- Understanding basophil surface marker expression is crucial for differentiating them from other myeloid cells and identifying their activation state.
Purpose of the Study:
- To comprehensively characterize the membrane marker profile of human basophils.
- To identify unique surface antigens expressed by basophils, potentially indicating activation.
Main Methods:
- Utilized a panel of 60 monoclonal antibodies (MoAbs) for combined toluidine/immunofluorescence staining.
- Analyzed basophil surface markers on cells in suspension and purified fractions, including those from chronic granulocytic leukemia (CGL) patients.
- Employed flow cytometry (FACS) for detailed analysis.
Main Results:
- Basophils express myeloid-associated markers (e.g., LFA-1 family, CDw17, CDw13, CDw12, VIM-2), indicating a relationship with other myeloid cells.
- Basophils uniquely express activation-linked structures (p45, p24, interleukin-2 receptor) not found on mature neutrophils.
- Under culture conditions, basophils express HLA-DR and T4 antigens; 3-fucosyl-N-acetyllactosamine is expressed after neuraminidase treatment.
- Basophils did not stain with MoAbs against Fc gamma-receptor (50-70 kd), CDw12, or CDw14, differentiating them from neutrophils and monocytes.
Conclusions:
- Human basophils possess a unique combination of surface determinants.
- Basophils may represent an inherently activated cell population.
- The distinct marker profile aids in understanding basophil function and differentiation.