TY - JOUR
T1 - Cyclosporin A blocks surface IgM‐mediated growth inhibition in an immature B lymphoma, BKS‐2
AU - Udhayakumar, Venkatachalam
AU - Muthukkumar, Subramanian
AU - Subbarao, Bondada
PY - 1991/10
Y1 - 1991/10
N2 - Cyclosporin A (CSA) is an immunosuppressive drug, which blocks selective activation pathways in T and B cells. Antigen receptor‐mediated signaling events have been shown to be very sensitive to CSA. Signaling through the surface IgM receptor had been shown to induce growth inhibition in immature B cell lymphoma cells. In this report, we demonstrate that CSA caused significant reversal of growth inhibition induced by an anti‐μ antibody in an immature B lymphoma, BKS‐2. Time‐course experiments indicated that CSA was completely effective when added as late as 4 h after the addition of ligand. CSA was also found to have no direct effect on anti‐μ‐induced Ca2+ elevation. These results suggest that the likely target for CSA lies downstream from the initial generation of second messengers, such as Ca2+.
AB - Cyclosporin A (CSA) is an immunosuppressive drug, which blocks selective activation pathways in T and B cells. Antigen receptor‐mediated signaling events have been shown to be very sensitive to CSA. Signaling through the surface IgM receptor had been shown to induce growth inhibition in immature B cell lymphoma cells. In this report, we demonstrate that CSA caused significant reversal of growth inhibition induced by an anti‐μ antibody in an immature B lymphoma, BKS‐2. Time‐course experiments indicated that CSA was completely effective when added as late as 4 h after the addition of ligand. CSA was also found to have no direct effect on anti‐μ‐induced Ca2+ elevation. These results suggest that the likely target for CSA lies downstream from the initial generation of second messengers, such as Ca2+.
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U2 - 10.1002/eji.1830211043
DO - 10.1002/eji.1830211043
M3 - Article
C2 - 1915562
AN - SCOPUS:0026048328
SN - 0014-2980
VL - 21
SP - 2605
EP - 2608
JO - European Journal of Immunology
JF - European Journal of Immunology
IS - 10
ER -