IgD attenuates the IgM-induced anergy response in transitional and mature B cells
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Sabouri, Zahra
Perotti, Samuel
Spierings, Emily
Humburg, Peter
Yabas, Mehmet
Bergmann, Hannes
Horikawa, Keisuke
Roots, Carla
Lambe, Samantha
Young, Clara
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Macmillan Publishers Ltd
Abstract
Self-tolerance by clonal anergy of B cells is marked by an increase in IgD and decrease in IgM antigen receptor surface expression, yet the function of IgD on anergic cells is obscure. Here we define the RNA landscape of the in vivo anergy response, comprising 220 induced sequences including a core set of 97. Failure to co-express IgD with IgM decreases overall
expression of receptors for self-antigen, but paradoxically increases the core anergy response,
exemplified by increased Sdc1 encoding the cell surface marker syndecan-1. IgD expressed on
its own is nevertheless competent to induce calcium signalling and the core anergy mRNA response. Syndecan-1 induction correlates with reduction of surface IgM and is exaggerated
without surface IgD in many transitional and mature B cells. These results show that IgD attenuates the response to self-antigen in anergic cells and promotes their accumulation. In this way, IgD minimizes tolerance-induced holes in the pre-immune antibody repertoire.
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Nature Communications
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Open Access
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