Related Experiment Video
Updated: Apr 28, 2026

08:25
Flow Cytometric Characterization of Murine B Cell Development
Published on: January 22, 2021
17.7K
Themis2 is not required for B cell development, activation, and antibody responses
Harald Hartweger1, Edina Schweighoffer1, Sophia Davidson1
1Medical Research Council, National Institute for Medical Research, London NW7 1AA, United Kingdom; and.
Journal of Immunology (Baltimore, Md. : 1950)
|June 8, 2014
Summary
Themis2 protein is present in B cells but is not essential for B cell development, activation, or antibody responses. This study reveals Themis2
Area of Science:
- Immunology
- Molecular Biology
Background:
- Themis1 protein is involved in T cell receptor (TCR) signaling.
- Themis2, a related protein, is expressed in B cells and interacts with signaling molecules like Grb2 and Vav1.
- Themis2 is proposed to transduce B cell receptor (BCR) signals, impacting B cell function.
Purpose of the Study:
- To investigate the expression pattern of Themis2 in various B cell subsets.
- To determine the physiological role of Themis2 in B cell development, activation, and antibody production.
Main Methods:
- Generated a Themis2-deficient mouse model.
- Analyzed Themis2 expression across different B cell populations.
- Assessed B cell development, activation, and antibody responses in wild-type and Themis2-deficient mice.
Main Results:
- Themis2 is expressed in all B cell subsets, including developing, mature, and activated cells.
- B cell activation leads to decreased Themis2 expression.
- Themis2-deficient mice exhibit normal B cell development, activation, and antibody responses.
Conclusions:
- Themis2 is dispensable for B cell development, activation, and humoral immunity.
- Despite its presence and association with signaling proteins, Themis2 does not play a critical role in BCR signaling or B cell function.
More Related Videos
Related Concept Videos
B Cell Activation and Differentiation
14.3K
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...
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...
14.3K
Cells of the Adaptive Immune Response
6.8K
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...
6.8K
T Cell Activation and Clonal Selection
13.6K
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...
Naive T cells that have not yet encountered an antigen express two primary CD...
13.6K
Development of Immunocompetence
1.2K
The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
1.2K
T Cell Types and Functions
3.2K
When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
3.2K
Humoral Immune Responses
65.9K
Overview
65.9K

