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Published on: January 7, 2019
Normal lymphocyte development but delayed humoral immune response in CD81-null mice
1Department of Medicine and Oncology, Stanford University Medical Center, California 94305, USA.
Insights
CD81 is not essential for T cell development. However, CD81 deficiency impacts B cell function, reducing CD19 expression and antibody production efficiency.
Area of Science:
- Immunology
- Molecular Biology
- Cell Biology
Background:
- CD81 is a cell surface molecule involved in B cell signaling complexes.
- Previous research suggested CD81's role in thymocyte maturation.
Purpose of the Study:
- To investigate the role of CD81 in T cell and B cell development and function.
- To determine if CD81 is essential for thymocyte maturation.
Main Methods:
- Gene targeting to create CD81-null mice.
- Analysis of thymocyte, T cell, and B cell populations.
- Assessment of antibody responses to ovalbumin.
Main Results:
- CD81-null mice exhibit normal thymocyte and T cell development.
- B cell numbers are normal in CD81-null mice, but CD19 expression is reduced.
- Early antibody responses are weaker in CD81-null mice.
Conclusions:
- CD81 is not required for T cell maturation.
- CD81 plays a role in optimal CD19 expression on B cells.
- CD81 is important for efficient B cell antibody production.
Abstract:
CD81 is a cell surface molecule expressed on many cell types and associated with the CD19/CD21/Leu13 signal-transducing complex on B cells. A recent report implies that CD81 expression on thymic stromal cells is important in the maturation of thymocytes from CD4-CD8- to CD4+CD8+. However, we have produced CD81-null mice by gene targeting, and find that they undergo normal development of thymocytes and express normal numbers of T cells. B cells are also found in normal numbers in the spleen, blood, and peritoneal cavity of CD81-null mice, but they express a lower level of CD19 compared to heterozygous littermates. Finally, early antibody responses to the protein antigen ovalbumin are weaker in CD81-null mice compared to their heterozygous littermates. This is consistent with the proposed role of the CD19/CD21/CD81-signaling complex in lowering the threshold for B cell responses. These results show that CD81 is not required for maturation of T cells, but is important for optimal expression of CD19 on B cells and optimal stimulation of antibody production.
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