A CD2-green fluorescence protein-transgenic mouse reveals very late antigen-4-dependent CD8(+) lymphocyte rolling in inflamed venules

Intravital microscopy allows detailed analysis of leukocyte trafficking in vivo, but fails to identify the nature of leukocytes investigated. Here, we describe the development of a CD2-enhanced green fluorescence protein (EGF P)-transgenic mouse to characterize lymphocyte trafficking during inflammat ion in vivo. A CD2-EGFP plasmid construct including the CD2 promoter, the E GFP transgene, and the CD2 locus control region was injected into B6CBA/F-1 pronuclei. EGFP(+) offspring were backcrossed into C57BL/6 mice for six ge nerations. Flow cytometry demonstrated that all peripheral blood EGFP(+) ce lls were positive for CD2 and negative for the granulocyte Ag Ly 6-G (GR-1) . EGFP(high) cells stained positive for CD2, CD3, CD8, TCR beta -chain, and NK1.1 but did not express the B cell and monocyte markers CD45RA, CD19, an d CD11b. In vitro stimulation assays revealed no difference in lymphocyte p roliferation and IL-2 secretion between EGFP(+) and EGFP(-) mice. Intravita l microscopy of untreated or TNF-alpha -treated cremaster muscle vernules s howed EGFP(+) cells in vivo, but these cells did not roll or adhere to the vessel wall. In cremaster muscle venules treated with both TNF-alpha and IF N-gamma EGFP(high) cells rolled, adhered, and transmigrated at a rolling ve locity slightly higher (11 mum/s) than that of neutrophils (10 mum/s). Bloc king alpha (4) integrin with a mAb increased rolling velocity to 24 mum/s. These findings show that CD8(+) T cells roll in TNF-alpha /IFN-gamma -pretr eated vessels in vivo via an alpha (4) integrin-dependent pathway.