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Flow Cytometric Characterization of Murine B Cell Development
Published on: January 22, 2021
MYC expression and distribution in normal mature lymphoid cells.
1Department of Pathology, University of Milano-Bicocca and San Gerardo Hospital, Via Pergolesi 33, Monza, Italy. giorgio.cattoretti@unimib.it
The Journal of Pathology
|November 21, 2012
Summary
The proto-oncogene MYC is primarily found in mature B cells within lymphoid tissue. This study establishes MYC
Area of Science:
- Immunology
- Molecular Biology
- Oncology
Background:
- The distribution of the MYC proto-oncogene product in lymphoid tissue remains poorly understood due to technical challenges.
- Previous studies were limited by antibody sensitivity, specificity, and the low abundance and short half-life of MYC.
- A clear understanding of MYC expression is crucial for comprehending B cell biology and oncogenesis.
Purpose of the Study:
- To validate antibodies for MYC detection in lymphoid tissues.
- To define the expression and distribution of MYC in mature normal lymphoid cells using multiparametric immunophenotyping.
- To clarify MYC's role in different B cell subsets and its cell cycle association.
Main Methods:
- Validation of two antibodies for MYC detection using flow cytometry and immunohistochemistry.
- Analysis of normal human tonsil tissue.
- Multiparametric immunophenotyping to identify MYC-expressing cell populations.
Main Results:
- MYC is predominantly expressed in B cells, including activated, cycling blasts (CD30+, IRF4+, AID±) and resting B lymphocytes (follicular mantle, memory B cells, FcRH4/IRTA1+ B cells).
- MYC is also found in germinal center founder cells and light zone germinal center cells.
- MYC expression occurs across all cell cycle phases in activated/mature B cells, but is rare in other lymphoid types.
Conclusions:
- Validated antibodies enable precise mapping of MYC expression in normal lymphoid tissue.
- MYC expression is a feature of diverse mature and activated B cell subsets.
- The observed MYC distribution partially differs from previous ex vivo and extractive experimental predictions.
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