Telomerase activity is induced in human peripheral B lymphocytes by the stimulation to antigen receptor

H Igarashi1, N Sakaguchi

  • 1Department of Immunology, Kumamoto University School of Medicine, Japan.

Blood
|February 15, 1997
PubMed

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.

Related Concept Videos

Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
Diversity of Antigen Receptors01:28

Diversity of Antigen Receptors

Antigen receptors are essential components of the immune system crucial in defending the body against foreign invaders. These receptors are present on the surface of B and T cells, enabling them to recognize antigens and mount an appropriate immune response.
Before encountering any antigen, lymphocytes express these receptors. On B cells, the antigen receptor is a membrane-bound antibody molecule called BCR; on T cells, it is a T cell receptor or TCR. B and T cell receptors are composed of two...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...