Gc. Starling et al., CHARACTERIZATION OF MOUSE CD6 WITH NOVEL MONOCLONAL-ANTIBODIES WHICH ENHANCE THE ALLOGENEIC MIXED LEUKOCYTE REACTION, European Journal of Immunology, 26(4), 1996, pp. 738-746
Human CD6 is a cell surface protein expressed by thymocytes, mature T
cells, a subset of B cells and certain cells of the brain. On human T
cells, CD6 has been shown to act as a co-stimulatory molecule which mo
dulates T cell receptor (TCR)-mediated T cell activation. To study Fur
ther the recently identified mouse CD6 (mCD6), we generated and charac
terized a set of anti-mCD6 mAb. Anti-mCD6 mAb recognizing the mCD6 sca
venger receptor cysteine-rich (SRCR) extracellular domains 1 and 3 wer
e identified. mAb against SRCR domain 3, but not domain 1, inhibited t
he interaction of CD6 with a recently identified ligand. activated leu
kocyte cell adhesion molecule (ALCAM). Immunohistochemical analysis in
dicated that mCD6 expression was largely localized to the T cell areas
of lymphoid tissue and, as previously reported in the human, CD6 was
also expressed by neurons. CD6 was highly expressed on mouse T cells i
solated from the spleen, lymph node and thymus as demonstrated by two-
color immunofluorescence analysis. The CD4(-) and CD8(+) cells in thes
e lymphoid compartments expressed similar levels of CD6. Immunoprecipi
tation studies showed mouse thymocytes predominantly express a CD6 iso
form of similar to 130 kDa. while splenocytes predominantly express a
CD6 isoform of similar to 100 kDa. Anti-mCD6 mAb enhanced allogeneic m
ixed leukocyte reactions (MLR). indicating that CD6-ALCAM interactions
may regulate the proliferative capacity of T cells.