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Updated: Aug 14, 2026

Generation of Human CD40-activated B cells
Published on: October 17, 2009
Telomerase activity is induced in human peripheral B lymphocytes by the stimulation to antigen receptor
1Department of Immunology, Kumamoto University School of Medicine, Japan.
Insights
Telomerase activity is induced in human B cells upon activation of the B-cell antigen receptor (BCR). This induction requires costimulation, such as with anti-CD40, and is linked to B-cell proliferation.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- B cells are crucial for adaptive immunity.
- Telomerase activity is essential for cellular proliferation and genomic stability.
- Understanding B cell activation is key to immune response research.
Purpose of the Study:
- To investigate the induction of telomerase activity in human B cells.
- To explore the molecular events regulating B cell proliferation via B-cell antigen receptor (BCR) stimulation.
- To identify signaling pathways involved in telomerase induction during B cell activation.
Main Methods:
- Human peripheral B cells were stimulated in vitro via BCR.
- Telomerase activity was measured following stimulation with anti-IgM antibodies, cytokines (IL-2, IL-4, IL-13), and anti-CD40 monoclonal antibodies.
- B cell proliferation was assessed.
- The role of phosphoinositide 3-kinase (PI3K) was investigated.
Main Results:
- Unstimulated B cells showed no detectable telomerase activity.
- Anti-IgM beads induced telomerase activity.
- Costimulation with cytokines or anti-CD40 was necessary when using soluble anti-IgM antibodies.
- Telomerase induction correlated with B cell proliferation but not strictly with growth extent.
- Phorbol dibutylate/calcium ionophore also induced telomerase activity.
- PI3K signaling appears to play a role in this induction.
Conclusions:
- Telomerase activity is induced during B cell activation, particularly in response to BCR stimulation and costimulatory signals.
- This finding provides insights into the molecular mechanisms of B cell proliferation in antigen-specific immune responses.
- The study highlights the role of specific signaling pathways in regulating telomerase in activated lymphocytes.
Abstract:
To understand the molecular events for the proliferation of B cells, we studied the induction of telomerase activity in vitro after stimulation to B-cell antigen receptor (BCR) on human peripheral B cells. Although unstimulated purified B cells of tonsils and peripheral blood from healthy volunteers do not express detectable telomerase activity, anti-IgM beads induce telomerase activity in these B cells. Soluble anti-IgM antibody (Ab) alone does not induce telomerase activity, but the second signal, given by either one of the cytokines of interleukin-2 (IL-2), IL-4, and IL-13 or by anti-CD40 monoclonal Ab (MoAb), is effective as the costimulation for the induction of the activity. Stimulation with anti-IgM Ab and anti-CD40 MoAb induces telomerase activity in most mature B cells of the tonsils and peripheral blood. The stimuli to both IgM and IgD receptors similarly induce the activity. Induction of telomerase activity is accompanied with the proliferation of B cells, but is not absolutely correlated with the extent of B-cell growth. Phorbol dibutylate (PDB) plus calcium (Ca) ionophore (PDB/Ca), which replace the activation through BCR and the costimulatory molecules, also induce telomerase activity. Moreover, it is suggested that phosphoinositide (PI) 3-kinase plays a role for the induction of telomerase activity in B cells stimulated with anti-IgM Ab and anti-CD40 MoAb. These results suggest that telomerase activity is induced in the B-cell activation of the antigen specific immune response.
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