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KMID : 0357119950170010017
Korean Journal of Immunology
1995 Volume.17 No. 1 p.17 ~ p.26
Expression of ICAM-1 and HLA-DR Induced by IFN-¥ã in Human Bladder Cancer Cell Lines
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Abstract
Four human bladder cancer cell lines, RT4(gI, well differentiated, superficial TCC), T24(GII, epidermoid, superficial TCC), J82(GIII, anaplastic, invasive TCC0, TCCSUP(GIV, distant metastatic TCC) and one normla fetus bladder cell line,
FHs7381B1,
were
analyzed for their ability to expres the ICAM-I and ILA-DR molecules at the trancriptional level as well as on their cell surfaces before and after treatment with 200U/ml of IFN-¥í. All cell lines except RT4, even though the intensity of ICAM-1
expression was enormously stronger in normal fetus blader cell line comparing to T24, J82 and TCCSUP, displayed consitutive expression of ICAM-1 before and after IFN-¥í treament. RT4 cells did not express ICAM-1 regardless of IFN-¥ítreamtnet.
Before
IFN-¥ítreamtnet, HLA-DR was not constitutively expressed in all cell lines. After 200U/ml of IFN-¥í treament, RT4 derived from patient with benign clinical course and j82 derived from patient without distant metastasis displayed elevated levels
of
HLADR
expression which reached to the almost maximum level after IFN-¥ítreament for 48hr. The exprsion rate and the degree of HLA-DR expression in these cell lines increased in a time dependent manner but HLA-DR expresion was not induced in the T24 and
TCCSUP
cell lines even at a higher concentration (1000U/mll) of IFN-¥í.
The molecular mechanism underlying such a differential expression was investigated and the HLA-DR gene regulation was studied at the transcriptional level. In RT4 and J82 cell lines, treatment with IFN-¥íled to the steady-state mRNA augmentation
of
the
HLA-DR gene. The HLA-DR A mRNA augmentotion was similar in both cell lines, whereas HLA-DR B mRNA augmentation was higher in RT4 than in J82. These results established that the human bladder cancer cell studied here showed a diffential
susceptibility to
IFN-¥íon the modulation of HLA-DR molecules, and this modulation is transcriptioally regulated.
By analysing above findings along with clinical characteristics of patients from whom the cell lines were stablished, it might be also suggested that the expression of ICAM-1 seems to be associated with cell differentiation and the iducibility of
HLA-DR
expression by IFN-¥íseems to be associated with clinical course and/or metastatic potential of bladder cancer.
KEYWORD
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