TY - JOUR
T1 - Effects of dimethyl sulfoxide treatment on h-2 expression and susceptibility to NK - or cytotoxic T - lymphocyte - mediated lysis of the YAC-1 lymphoma and its β2-microglobulin - deficient variant
AU - Yamasaki, Toshiki
AU - Klein, George
AU - Ljunggren, Hans Gustaf
AU - Höglund, Petter
AU - öhlén, Claes
AU - Petersson, Max G.E.
AU - Kärre, Klas
N1 - Funding Information:
'Received September 2, 1987; accepted September 21, 1987. Supported by Public Health Service grant 5-R01CA-25250-06 from the National Cancer Institute, National Institutes of Health, Department of Health and Human Services; and by grants from the Swedish Cancer Society. 3 Department of Tumor Biology, Karolinska Institute, Box 60400 S-104 01, Stockholm, Sweden. 4 Department of Immunology, Karolinska Institute. 5 We gratefully acknowledge Ms. Maj-Lis Solberg and Ms. Margareta Hagelin for technical assistance and Mr. Anders Carstensen (Department of Tumor Biology, Karolinska Institute) for assistance with FACS analysis.
PY - 1988/4/20
Y1 - 1988/4/20
N2 - The effects of dimethyl sulfoxide (DMSO) on H-2 expression and susceptibility to NK-and cytotoxic T-lymphocyte (CTL)-mediated lysis in the murine T-cell lymphoma YAC-1 and its beta-2-microglobulin (β2m)- deficient variant were studied. Fluorescence-activated cell sorter analysis revealed induction of H-2kk and βm 3 days after culture of YAC-1 with DMSO, where optimal H-2Dd induction required more than 1 week. H-2Kk and H-2Dd induction by DMSO was equal to preteatment of YAC-1 cells with 50-100 and 10-20 U/ml interferon (IFN)-gamma, respectively, but the T-cell differentation antigens Lyt-1, Lyt-2, Thy-1, and L3T4 remained unaffected. DMSO Protected YAC-1 cells from NK lysis as efficently as 10-20 UIFN/ml, whereas susceptibility to anti-H-2a-, H-2Kk-, and H-2Dd-specific CTLs Was augmented as in IFN-treated YAC-1 cells. In contrast, the β2m-deficient variant, which remained H-2 negative at the cell surface after DMSON treatment, also remained NK sensitive. Thus DMSO can induce H-2 expression and alter the sensitivity of murine lymphoma cells to different effector cells. [J Natl Cancer Inst 1988;80:263-269]
AB - The effects of dimethyl sulfoxide (DMSO) on H-2 expression and susceptibility to NK-and cytotoxic T-lymphocyte (CTL)-mediated lysis in the murine T-cell lymphoma YAC-1 and its beta-2-microglobulin (β2m)- deficient variant were studied. Fluorescence-activated cell sorter analysis revealed induction of H-2kk and βm 3 days after culture of YAC-1 with DMSO, where optimal H-2Dd induction required more than 1 week. H-2Kk and H-2Dd induction by DMSO was equal to preteatment of YAC-1 cells with 50-100 and 10-20 U/ml interferon (IFN)-gamma, respectively, but the T-cell differentation antigens Lyt-1, Lyt-2, Thy-1, and L3T4 remained unaffected. DMSO Protected YAC-1 cells from NK lysis as efficently as 10-20 UIFN/ml, whereas susceptibility to anti-H-2a-, H-2Kk-, and H-2Dd-specific CTLs Was augmented as in IFN-treated YAC-1 cells. In contrast, the β2m-deficient variant, which remained H-2 negative at the cell surface after DMSON treatment, also remained NK sensitive. Thus DMSO can induce H-2 expression and alter the sensitivity of murine lymphoma cells to different effector cells. [J Natl Cancer Inst 1988;80:263-269]
UR - http://www.scopus.com/inward/record.url?scp=0023892304&partnerID=8YFLogxK
U2 - 10.1093/jnci/80.4.263
DO - 10.1093/jnci/80.4.263
M3 - Article
C2 - 3127594
AN - SCOPUS:0023892304
SN - 0027-8874
VL - 80
SP - 263
EP - 269
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 4
ER -