期刊
JOURNAL OF IMMUNOLOGY
卷 167, 期 9, 页码 5018-5026出版社
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.167.9.5018
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IL-5 stimulation of CD38-activated murine splenic B cells induces mu-gammal CSR at the DNA level leading to a high level of IgG1 production. Further addition of IL-4 in the system enhances IL-5-dependent mu-gammal CSR. Although some of the postreceptor signaling events initiated by IL-5 in activated B cells have been characterized, the involvement of Stat in IL-5 signaling has not been thoroughly evaluated. In this study, we examined the activation of Stat5 and activation-induced cytidine deaminase (AID) in CD38-activated murine splenic B cells by IL-5. The role of Stat5a and Stat5b in IL-5-induced mu-gammal CSR and also IgG1 and IgM production was documented, as IL-5 does not act on CD38-stimulated splenic B cells from Stat5a(-/-) and Stat5b(-/-) mice. Expression levels of CD38-induced germline gamma1 transcripts and AID in Stat5a-/- and Stat5b-/- B cells upon IL-5 stimulation were comparable to those of wild-type B cells. The impaired mu-gammal CSR by Stat5b-/- B cells, but not by Stat5a-/- B cells, was rescued in part by IL-4, as the addition of IL-4 to the culture of CD38- and IL-5-stimulated B cells induced mu-gammal CSR leading to IgG1 production. Analysis of cell division cycle number of wild-type B cells revealed that mu-gammal CSR was observed after five or six cell divisions. Stat5a(-/-) and Stat5b(-/-) B cells showed similar cell division cycles, but they did not undergo mu-gammal CSR. Our data support the notion that both Stat5a and Stat5b are essential for IL-5-dependent mu-gammal CSR and Ig secretion; however, their major target may not be AID. Stat5a and Stat5b are not redundant, but rather are at least partially distinctive in their function.
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