Genetic control of HgCl sub(2)-induced IgE and autoimmunity by a 117-kb interval on rat chromosome 9 through CD4 CD45RC super(high) T cells

Gold or mercury salts trigger a dramatic IgE response and a CD4 T-cell-dependent nephropathy in Brown-Norway (BN), but not in Lewis (LEW) rats. We previously identified the 1.1-Mb Iresp3 (immunoglobin response QTL3) locus on chromosome 9 that controls these gold salt-triggered immune disorders. In the present work, we investigated the genetic control of HgCl sub(2)-induced immunological disorders and assessed the relative contribution of the CD45RC super(high) and CD45RC super(low) CD4 T-cell subpopulations in this control. By using interval-specific congenic lines, we narrowed down Iresp3 locus to 117-kb and showed that BN rats congenic for the LEW 117-kb were protected from HgCl sub(2)-triggered IgE response and nephropathy. This 117-kb interval also controls CD45RC expression by CD4 T cells and the ability of CD45RC super(high) CD4 T cells to trigger the autoimmune disorders resulting from HgCl sub(2) administration. This 117-kb region contains four genes, including Vav1, a strong candidate gene according to its cellular function and exclusive expression in hematopoietic cells. Thus, this study highlights the role of the CD45RC super(high) CD4 T-cell subpopulation in the opposite susceptibility of BN and LEW rats to HgCl sub(2)-triggered immune disorders and identifies a 117-kb interval on chromosome 9 that has a key role in their functions.