Islet-reactive T-cell clones from NOD mice provide an important approa
ch to the investigation of antigens with relevance to type I diabetes.
To identify a source of beta-cell antigen suitable for biochemical st
udies, we have used two islet-specific, diabetogenic T-cell clones to
test beta-tumor cells. beta-tumor cell lines, maintained in continuous
culture, were found to lose antigenicity rapidly. However, cells harv
ested directly from beta-tumors arising spontaneously in the transgeni
c NOD/Lt-Tg(RIPTag)1Lt mouse proved to be a potent source of beta-cell
antigen for the T-cell clones. Subcellular fractionation of beta-tumo
r cells showed that the T-cell antigen was highly enriched in the beta
-granule fraction and that this activity was associated with the granu
le membrane.