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Updated: Aug 8, 2026

Generation of Human CD40-activated B cells
Published on: October 17, 2009
Characterization of the common acute lymphoblastic leukaemia antigen (CD10) as an activation molecule on mature human
N Kiyokawa1, Y Kokai, K Ishimoto
1Department of Pathology, National Children's Medical Research Centre, Tokyo, Japan.
Insights
CD10 is transiently expressed early in B cell activation, distinct from other activation markers. This pattern mirrors Burkitt
Area of Science:
- Immunology
- Cell Biology
- Hematology
Background:
- CD10 is a cell surface marker with a known role in B cell development.
- The precise expression pattern of CD10 during B cell activation requires further elucidation.
- Understanding B cell activation markers is crucial for diagnosing and classifying lymphoid malignancies.
Purpose of the Study:
- To analyze the distinct expression pattern of CD10 during B cell activation.
- To investigate the relationship between CD10 expression and other activation markers.
- To explore the potential role of CD10 expression in the histogenesis of Burkitt's lymphoma.
Main Methods:
- Two-color flow cytometry was used to analyze CD10 expression on activated B cells.
- In vivo and in vitro systems were employed to study B cell activation.
- Cell fractionation by gravity was performed to separate cell populations based on antigen expression.
- Immunophenotyping of Burkitt's lymphoma cases was conducted.
Main Results:
- CD10 is expressed at a specific, transient early stage of B cell activation, distinct from other activation antigens.
- CD10+ B cells could be separated from cells expressing other activation markers and some CD10+ cells also expressed the resting B cell antigen L30.
- In vitro, CD10+ B cells emerged early and disappeared late during activation.
- All analyzed Burkitt's lymphoma cases expressed CD10, with a high co-expression of L30 and L29.
Conclusions:
- CD10 is a transiently expressed early activation antigen on B cells.
- The immunophenotype of Burkitt's lymphoma suggests a resemblance to early-stage activated B cells co-expressing CD10 and L30.
- This study provides insights into the precise expression dynamics of CD10 and its implications for understanding Burkitt's lymphoma.
Abstract:
Distinct expression pattern of CD10 molecules during B cell activation was analysed using in vivo and in vitro systems. By two-colour flowcytometrical analysis, CD10 was found to be expressed at a specific stage of in vivo activating B cells. The expression of CD10 during B cell activation appeared to be unique from that of other activation-related B cell antigens including L29, MA6, OKT9 and OKT10. Although the expression of CD10 was associated with that of the activation-related B cell antigens, CD10+ B cells could be separated in the distinct fractions to those expressing other activation-related B cell antigens when fractionated by cell gravity. In particular, certain CD10+ B cells were detected positive for the resting B cell antigen, L30. In vitro studies revealed that CD10+ B cells arose from CD10- B cells at an early step of B cell activation, and disappeared lately when activated by Staphylococcus aureus Cowan I. Collectively, CD10 was an antigen transiently expressed at an early phase of B cell activation process. Expression of CD10 and other antigens on Burkitt's lymphomas (15 cases) was studied next. All cases were CD10+, and 87% (13 cases) were also L30+. In addition, six of CD10+ L30+ cases were L29+. This observation suggested that Burkitt's lymphomas were phenotypically similar to the B cells at an early phase of activation, those expressing CD10 and L30, simultaneously. The present study has dissected a precise expression pattern of CD10 on mature B cell activation in vitro and in vivo, and could be implicated for the histogenesis of one of the poorly characterized B cell lymphoma, namely Burkitt's lymphoma.
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