Figure 4
Figure 4. TRAF3 mice develop autoimmunity. (A) Analysis of circulating autoantibodies in TRAF3 mice and wild-type littermates. Blood from TRAF3 mice (12-17 months old) and from wild-type littermates was extracted for serum collection. The presence of autoantibodies in serum was determined by ELISA (anti-dsDNA, 1:150 dilution; anti-ANA, anti-ssDNA, and anti-SSA/Ro, 1:50 dilution). Statistical significance was determined by unpaired Student t test. (B) Pathologic alterations in kidneys from TRAF3 mice. Morphologic lesions encompass both glomerular (i-xi) and tubulointerstitial (i,iii) alterations, demonstrated by H&E (i-iii), Jones silver methanamine (iv,v), and Masson trichrome (vi,vii) stains. Depositions of IgG (viii,ix) and C3 complement (x,xi) were detected by immunostaining. Bars, 50 μm.

TRAF3 mice develop autoimmunity. (A) Analysis of circulating autoantibodies in TRAF3 mice and wild-type littermates. Blood from TRAF3 mice (12-17 months old) and from wild-type littermates was extracted for serum collection. The presence of autoantibodies in serum was determined by ELISA (anti-dsDNA, 1:150 dilution; anti-ANA, anti-ssDNA, and anti-SSA/Ro, 1:50 dilution). Statistical significance was determined by unpaired Student t test. (B) Pathologic alterations in kidneys from TRAF3 mice. Morphologic lesions encompass both glomerular (i-xi) and tubulointerstitial (i,iii) alterations, demonstrated by H&E (i-iii), Jones silver methanamine (iv,v), and Masson trichrome (vi,vii) stains. Depositions of IgG (viii,ix) and C3 complement (x,xi) were detected by immunostaining. Bars, 50 μm.

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