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Updated: Jun 26, 2026

Generation of Human CD40-activated B cells
Published on: October 16, 2009
Expression of CD320 in human B cells in addition to follicular dendritic cells
Whajung Cho1, Jinsuk Choi, Chan-Hum Park
1Department of Microbiology and Immunology, Kangwon National University College of Medicine, Chuncheon, Korea.
Insights
The newly discovered CD320 protein is found in germinal center B cells, not just follicular dendritic cells. This finding suggests a more complex role for CD320 in B cell activity than previously understood.
Area of Science:
- Immunology
- Cell Biology
Background:
- CD320 is a recently identified protein associated with follicular dendritic cells (FDCs).
- Its known function involves enhancing germinal center (GC) B cell proliferation, but its cellular distribution is poorly understood.
Purpose of the Study:
- To investigate the cellular distribution of CD320 within the germinal center.
- To determine if CD320 is expressed by B cells in addition to FDCs.
Main Methods:
- Confocal microscopy was used to examine human tonsil sections for CD320 co-localization with B cell markers (CD19, CD38) and T cell marker (CD3).
- Reverse transcriptase-polymerase chain reaction (RT-PCR) was employed to confirm CD320 mRNA expression in purified GC B cells.
Main Results:
- CD320 was found to co-localize with CD19 and CD38 on GC B cells, indicating expression on these cells.
- CD320 expression was observed in the nucleus, membrane, and cytoplasm of purified GC B cells.
- CD320 mRNA was confirmed in B cells, further supporting its expression.
Conclusions:
- CD320 is expressed in GC B cells, expanding its known cellular distribution beyond FDCs.
- The presence of CD320 in B cells suggests a more intricate role in GC activity than initially presumed.
Abstract:
CD320 has been recently discovered and reported as a follicular dendritic cell (FDC) protein. Although CD320 is known to enhance proliferation of germinal center (GC) B cells, little other information is available. In this study, we investigated its cellular distribution in the GC. Confocal microscopy of human tonsil sections revealed co-localization of CD320 with CD19 and CD38 but not with CD3 indicating that GC B cells expressed CD320 in addition to FDC. In purified GC B cells, CD320 expression was inhibited in the nucleus, membrane and cytoplasm. Reverse transcriptase-polymerase chain reaction confirmed CD320 mRNA expression in B cells. These finding indicate that CD320 is expressed in B cells in addition to FDC, and that its GC activity may be more complicated than previously thought.
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