Essential role of Stat5 for IL-5-dependent IgH switch recombination in mouse B cells

J Immunol. 2001 Nov 1;167(9):5018-26. doi: 10.4049/jimmunol.167.9.5018.

Abstract

IL-5 stimulation of CD38-activated murine splenic B cells induces mu-gamma1 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-gamma1 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-gamma1 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-gamma1 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-gamma1 CSR leading to IgG1 production. Analysis of cell division cycle number of wild-type B cells revealed that mu-gamma1 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-gamma1 CSR. Our data support the notion that both Stat5a and Stat5b are essential for IL-5-dependent mu;-gamma1 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase
  • ADP-ribosyl Cyclase 1
  • Animals
  • Antigens, CD*
  • Antigens, Differentiation / pharmacology
  • B-Lymphocytes / metabolism*
  • Cytidine Deaminase / metabolism
  • DNA-Binding Proteins / physiology*
  • Immunoglobulin Class Switching*
  • Immunoglobulin G / biosynthesis*
  • Immunoglobulin G / classification
  • Immunoglobulin G / genetics
  • Immunoglobulin Heavy Chains / biosynthesis*
  • Immunoglobulin M / biosynthesis*
  • Immunoglobulin M / genetics
  • Interleukin-5 / pharmacology*
  • Lymphocyte Activation
  • Membrane Glycoproteins
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Milk Proteins*
  • NAD+ Nucleosidase / pharmacology
  • Positive Regulatory Domain I-Binding Factor 1
  • RNA, Messenger / analysis
  • Recombination, Genetic
  • Repressor Proteins*
  • STAT5 Transcription Factor
  • Trans-Activators / physiology*
  • Transcription Factors / biosynthesis

Substances

  • Antigens, CD
  • Antigens, Differentiation
  • DNA-Binding Proteins
  • Immunoglobulin G
  • Immunoglobulin Heavy Chains
  • Immunoglobulin M
  • Interleukin-5
  • Membrane Glycoproteins
  • Milk Proteins
  • Prdm1 protein, mouse
  • RNA, Messenger
  • Repressor Proteins
  • STAT5 Transcription Factor
  • Stat5a protein, mouse
  • Stat5b protein, mouse
  • Trans-Activators
  • Transcription Factors
  • Positive Regulatory Domain I-Binding Factor 1
  • ADP-ribosyl Cyclase
  • Cd38 protein, mouse
  • NAD+ Nucleosidase
  • ADP-ribosyl Cyclase 1
  • Cytidine Deaminase