Ku70 is required for late B cell development and immunoglobulin heavy chain class switching

被引:237
作者
Manis, JP
Gu, YS
Lansford, R
Sonoda, E
Ferrini, R
Davidson, L
Rajewsky, K
Alt, FW
机构
[1] Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Childrens Hosp, Boston, MA 02115 USA
[3] Ctr Blood Res, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[5] Kyoto Univ, Dept Mol Immunol & Allergy, Kyoto 60601, Japan
[6] Univ Cologne, Inst Genet, D-5000 Cologne 41, Germany
关键词
immunoglobulin class switch recombination; Ku70; recombination activating gene 2; B cell development;
D O I
10.1084/jem.187.12.2081
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunoglobulin (Ig) heavy chain (HC) class switch recombination (CSR) is a late B cell process that involves intrachromosomal DNA rearrangement. Ku70 and Ku80 form a DNA end-binding complex required for DNA double strand break repair and V(D)J recombination. Ku70(-/-) (K70T) mice, like recombination activating gene (RAG)-1- or RAG-2-deficient (R1T or R2T) mice, have impaired B and T cell development at an early progenitor stage, which is thought to result at least in part from defective V(D)J recombination (Gu, Y., IC.J. Seidl, G.A. Rathbun, C. Zhu, J.P. Manis, N. van der Steep, L. Davidson, H.L. Cheng, J.M. Sekiguchi, It. Frank, et al. 1997. Immunity. 7:653-665; Ouyang, H., A. Nussenzweig, A. Kurimasa, V.C. Soares, X. Li, C. Cordon-Cardo, W. Li, N. Cheong, M. Nussenzweig, G. Iliakis, et al. 1997.J. Exp.. Mcd. 186:921-929). Therefore, to examine the potential role of Ku70 in CSR, we generated K70T mice that carry a germline Ig HC locus in which the JH region was replaced with a functionally rearranged VH(D)JH and Ig lambda light chain transgene (referred to as K70T/HL mice). Previously, we have shown that B cells from R1T or R2T mice carrying these rearranged Ig genes (R1T/HL or R2T/HL mice) can undergo CSR to IgG isotypes (Lansford, R., J. Manis, E. Sonoda, K. Rajewsky, and F. Alt. 1998. Int. Immunol. 10.325-332). K70T/HL mice had significant numbers of peripheral surface IgM(+) B cells, which generated serum IgM levels similar to those of R2T/HL mice. However, in contrast to R2T/HL mice, K70T/HL mice had no detectable serum IgG isotypes. In vitro culture of K70T/HL B cells with agents that induce CSR in normal or R2T/HL B cells did lead to the induction of germline CH transcripts, indicating that initial signaling pathways for CSR were intact in K70T/HL cells. However, treatment with such agents did not lead to detectable CSII by K70T/HL B cells, and instead, led to cell death within 72 h. We conclude that Ku70 is required for the generation of B cells that have undergone Ig HC class switching. Potential roles for Ku70 in the CSR process are discussed.
引用
收藏
页码:2081 / 2089
页数:9
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