IDENTIFICATION AND CHARACTERIZATION OF RAT GAMMA DELTA T-LYMPHOCYTES IN PERIPHERAL LYMPHOID ORGANS, SMALL-INTESTINE, AND SKIN WITH A MONOCLONAL-ANTIBODY TO A CONSTANT DETERMINANT OF THE GAMMA/DELTA T-CELL RECEPTOR/
P. Kuhnlein et al., IDENTIFICATION AND CHARACTERIZATION OF RAT GAMMA DELTA T-LYMPHOCYTES IN PERIPHERAL LYMPHOID ORGANS, SMALL-INTESTINE, AND SKIN WITH A MONOCLONAL-ANTIBODY TO A CONSTANT DETERMINANT OF THE GAMMA/DELTA T-CELL RECEPTOR/, The Journal of immunology, 153(3), 1994, pp. 979-986
A mAb called V65 was raised to a CD3(+), TCR-alpha/beta(-) rat/mouse T
cell hybrid that selectively reacts with all CD3(+) TCR-alpha/beta(-)
rat lymphocytes. Both anti-CD3 and V65 precipitate a 48- to 50-kDa he
terodimeric protein from digitonin-lysed surface-iodinated cells. V65(
+) but not V65(-) T cells and T cell hybridoma cells express TCR-gamma
mRNA. Together, these results show that V65 detects a constant determ
inant of the rat TCR-gamma/delta. In the presence of either IL-2 or IL
-4, V65 stimulates proliferation in peripheral rat gamma/delta T cells
. Approximately 90% of gamma/delta T cells from peripheral lymphoid or
gans have the same cell surface phenotype as thymus-derived MHC class
I-restricted alpha/beta T cells, i.e., they are CD4(-) but express the
CD8 alpha/beta heterodimer together with CD2 and CD5. In contrast, ga
mma/delta T cells from the epithelium of the small intestine lack CD2,
CD4, and CD5 and express CD8 alpha only. Finally, V65 directly identi
fies a dense network of dendritic cells in the epidermis as gamma/delt
a T cells. These dendritic epidermal T cells are absent from athymic r
ats, indicating that like their mouse counterparts, they are thymus de
pendent.