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. 1997 Nov 17;186(10):1663–1676. doi: 10.1084/jem.186.10.1663

Figure 5.

Figure 5

Phenotype and functional activity of CD8+ T cells from RAG-2−/− versus RAG-2+ 8.3-NOD mice. (A) Flow cytometry profiles of CD4+CD8+ (left) and CD4CD8+ thymocytes (right) from 8.3-NOD mice (dotted line) and RAG-2−/− 8.3-NOD mice (solid line) for maturation markers. Thymocytes were analyzed by three-color cytofluorometry as in Fig. 1. Panels show the fluorescence histograms of each marker on gated CD4+CD8+ and CD4CD8+ thymocytes. (B) Flow cytometry profiles of splenic CD8+ T cells from 8.3-NOD mice (dotted line) and RAG-2−/− 8.3-NOD mice (solid line) for activation and memory markers. (C) Proliferative activity of splenic CD8+ T cells from 8.3-NOD mice and RAG-2−/− 8.3-NOD mice in response to islet cells. (D) Reverse transcription-PCR analysis for cytokine gene expression of islet-derived CD8+ T cells from 8.3-NOD mice and RAG-2−/− 8.3-NOD mice. M, 1Kb ladder. (E) Kinetics of insulitis in RAG-2−/− 8.3-NOD mice.