Genetic dissection of lupus pathogenesis: Sle3/5 impacts IgH CDR3 sequences, somatic mutations, and receptor editing

Masatoshi Wakui, Jinho Kim, Edward J. Butfiloski, Laurence Morel, Eric S. Sobel

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Sle3/5 is a lupus susceptibility locus identified on mouse chromosome 7 of the New Zealand Black/New Zealand White (NZB/ NZW)-derived NZM2410 strain. Based on previous observations, this locus appears to contribute to lupus pathogenesis through its impact on diversification of immune responses. To understand how Sle3/5 affects somatic diversification of humoral responses, we analyzed IgH rearrangements preferentially encoding hapten-reactive IgG1 repertoires after immunization and assessed peripheral IgH VDJ recombination activities in C57BL/6 (B6) mice coagenic for Sle3/5 (B6.Sle3/5). In addition to altered somatic VH mutation profiles, sequences from B6.Sle3/5 mice exhibited atypical IgH CDR3 structures characteristic of autoreactive B cells and consistent with peripheral B cells bearing putatively edited receptors. Significant expression of Rag genes and circular VHD gene excision products were detected in splenic mature B cells of B6.Sle3/5 but not B6 mice, showing that peripheral IgH rearrangements occurred beyond allelic exclusion. Taken together, on the nonautoimmune background, Sle3/5 affected V HDJH junctional diversity and VH mutational diversity and led to recombinational activation of allelically excluded IgH genes in the periphery. Such impact on somatic IgH diversification may contribute to the development of autoreactive B cell repertoires. This is the first report to present evidence for significant association of a lupus susceptibility locus, which has been mapped to a chromosomal region in which no Ig genes have been identified, with somatic IgH sequence diversity and peripheral H chain receptor editing or revision without relying upon Ig transgene strategies.

Original languageEnglish
Pages (from-to)7368-7376
Number of pages9
JournalJournal of Immunology
Volume173
Issue number12
Publication statusPublished - 2004 Dec 15
Externally publishedYes

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Dissection
B-Lymphocytes
Mutation
New Zealand
V(D)J Recombination
Immunoglobulin Genes
Chromosomes, Human, Pair 7
Haptens
Transgenes
Genes
Immunization
Immunoglobulin G
Gene Expression

ASJC Scopus subject areas

  • Immunology

Cite this

Genetic dissection of lupus pathogenesis : Sle3/5 impacts IgH CDR3 sequences, somatic mutations, and receptor editing. / Wakui, Masatoshi; Kim, Jinho; Butfiloski, Edward J.; Morel, Laurence; Sobel, Eric S.

In: Journal of Immunology, Vol. 173, No. 12, 15.12.2004, p. 7368-7376.

Research output: Contribution to journalArticle

Wakui, Masatoshi ; Kim, Jinho ; Butfiloski, Edward J. ; Morel, Laurence ; Sobel, Eric S. / Genetic dissection of lupus pathogenesis : Sle3/5 impacts IgH CDR3 sequences, somatic mutations, and receptor editing. In: Journal of Immunology. 2004 ; Vol. 173, No. 12. pp. 7368-7376.
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