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In vitro and in vivo expression of a nephritogenic Ig heavy chain determinant: Pathogenic autoreactivity requires permissive light chains
Author(s) -
Cooperstone Brenda G,
Rahman Mohammed M,
Rudolph Earl H,
Foster Mary H
Publication year - 2001
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1046/j.1440-1711.2001.01001.x
Subject(s) - biology , microbiology and biotechnology , antibody , immunoglobulin heavy chain , immunoglobulin light chain , immunology
Lymphocyte antigen receptors are promising targets for immune intervention strategies in disorders marked by repertoire skewing or expansion of lymphocyte subsets. Appropriate application of immune receptor modulation is predicated on understanding the role of a particular receptor in pathogenesis and disease regulation. The V H B/W16 gene, restricted to mice carrying the j haplotype for the J558 family, is overexpressed by murine lupus anti‐DNA Ig. This gene is also expressed recurrently among nephritogenic anti‐DNA Ig recovered from several autoimmune strains, suggesting that cells expressing this pathogenic receptor are positively selected during disease progression. To explore the extent and mechanisms by which Ig H chains expressing this gene contribute to autoimmunity, an Ig H chain gene was engineered for in vitro and in vivo recombination studies. Site‐directed mutagenesis generated unique restriction sites to link PCR‐amplified V region (VDJ) cDNA to previously isolated genomic fragments containing Ig regulatory and signal sequences. The new 3 kb VDJ gene was then ligated to a 9 kb fragment encoding the IgM constant region. Transfection of H chain loss variant myeloma with the complete 12 kb construct, termed 238H‐Cμ, resulted in secretion of intact Ig pairing 238H‐Cμ with a lambda L chain; however, transfectant Ig lacked autoreactivity and pathogenicity. Introduction of the 238H‐Cμ H chain as a transgene onto the non‐autoimmune C57BL/6 background resulted in abundant B cell surface expression of 238H‐Cμ, however, four transgenic Ig recovered by fusion of LPS‐stimulated splenocytes and formed by combination of 238H‐Cμ with endogenous kappa chains do not bind DNA or laminin. These results indicate that the antigen binding sites encoded by this disease‐associated gene and/or H chain must associate with permissive L chains to specify autoimmunity. The 238H‐Cμ transgenic model should prove useful in dissecting the in vivo fate of 238H‐Cμ‐L combinations that produce pathogenic autoreactive receptors and in evaluating receptor‐targeted interventions.