scholarly journals The Endocytic Adaptor Eps15 Controls Marginal Zone B Cell Numbers

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e50818 ◽  
Author(s):  
Benedetta Pozzi ◽  
Stefania Amodio ◽  
Caterina Lucano ◽  
Anna Sciullo ◽  
Simona Ronzoni ◽  
...  
Keyword(s):  
B Cell ◽  
2003 ◽  
Vol 33 (9) ◽  
pp. 2567-2576 ◽  
Author(s):  
Rhodri Ceredig ◽  
Nabil Bosco ◽  
Patrice N. Maye ◽  
Jan Andersson ◽  
Antonius Rolink

2001 ◽  
Vol 194 (8) ◽  
pp. 1151-1164 ◽  
Author(s):  
Zhenyue Hao ◽  
Klaus Rajewsky

To study homeostasis of peripheral B lymphocytes in the absence of B cell influx from the bone marrow, we generated a mouse mutant in which the recombination-activating gene (RAG)-2 can be inducibly deleted. When RAG-2 was deleted at the age of 8–10 wk, splenic naive follicular B cells were gradually lost over a year of observation, with a half-life of ∼4.5 mo. By contrast, the pool of marginal zone B cells in the spleen and of B-1 cells in the peritoneal cavity were kept at normal level. In lymph nodes, ∼90% of the B cells were lost within 4 mo, and B cell numbers remained constant thereafter. Mice in which RAG-2 was deleted at birth maintained a small population of activated B cells with an increased proportion of marginal zone B cells. Additionally, an increase of the pool of IgM secreting cells and B-1a cells was observed.


Author(s):  
Benedetta Pozzi ◽  
Stefania Amodio ◽  
Caterina Lucano ◽  
Anna Sciullo ◽  
Simona Ronzoni ◽  
...  
Keyword(s):  
B Cell ◽  

2021 ◽  
Vol 12 ◽  
Author(s):  
Kristina Ottens ◽  
Anne B. Satterthwaite

Strict control of B lymphocyte development is required for the ability to mount humoral immune responses to diverse foreign antigens while remaining self-tolerant. In the bone marrow, B lineage cells transit through several developmental stages in which they assemble a functional B cell receptor in a stepwise manner. The immunoglobulin heavy chain gene is rearranged at the pro-B stage. At the large pre-B stage, cells with a functional heavy chain expand in response to signals from IL-7 and the pre-BCR. Cells then cease proliferation at the small pre-B stage and rearrange the immunoglobulin light chain gene. The fully formed BCR is subsequently expressed on the surface of immature B cells and autoreactive cells are culled by central tolerance mechanisms. Once in the periphery, transitional B cells develop into mature B cell subsets such as marginal zone and follicular B cells. These developmental processes are controlled by transcription factor networks, central to which are IRF4 and IRF8. These were thought to act redundantly during B cell development in the bone marrow, with their functions diverging in the periphery where IRF4 limits the number of marginal zone B cells and is required for germinal center responses and plasma cell differentiation. Because of IRF4’s unique role in mature B cells, we hypothesized that it may also have functions earlier in B cell development that cannot be compensated for by IRF8. Indeed, we find that IRF4 has a unique role in upregulating the pre-B cell marker CD25, limiting IL-7 responsiveness, and promoting migration to CXCR4 such that IRF4-deficient mice have a partial block at the pre-B cell stage. We also find that IRF4 acts in early transitional B cells to restrict marginal zone B cell development, as deletion of IRF4 in mature B cells with CD21-cre impairs plasma cell differentiation but has no effect on marginal zone B cell numbers. These studies highlight IRF4 as the dominant IRF family member in early B lymphopoiesis.


2020 ◽  
Author(s):  
Barbara Vannata ◽  
Anna Vanazzi ◽  
Mara Negri ◽  
Sarah Jayne Liptrott ◽  
Anna Amalia Bartosek ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document