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Ionizing radiation modulates the surface expression of human leukocyte antigen-G in a human melanoma cell line
被引:21
作者:
Michelin, Severino
[1
]
Gallegos, Cristina E.
[1
]
Dubner, Diana
[1
]
Favier, Benoit
[2
]
Carosella, Edgardo D.
机构:
[1] Nucl Regulatory Author, Radiopathol Lab, Buenos Aires, DF, Argentina
[2] Hop St Louis, CEA, I2BM, Serv Rech Hematoimmunol,IUH, Paris, France
关键词:
gamma-Radiation;
HLA-G;
Melanoma;
Immune system;
Immunotolerance;
HLA-G EXPRESSION;
CLASS-I ANTIGEN;
FACTOR GENE-EXPRESSION;
TUMOR-CELLS;
G MOLECULES;
NITRIC-OXIDE;
EPIGENETIC FEATURES;
GAMMA-IRRADIATION;
T-CELL;
CANCER;
D O I:
10.1016/j.humimm.2009.07.030
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Human leukocyte antigen G (HLA-G) is a nonclassical HL-A class I molecule involved in fetus protection from the maternal immune system, transplant tolerance, and viral and tumoral immune escape. Tumor-specific HLA-G expression has been described for a wide variety of malignancies, including melanomas. The aim of this study was to evaluate whether ionizing radiation (IR) could modulate the surface expression of HLA-G1 in a human melanoma cell line that expresses endogenously membrane-bound HLA-G1. For this purpose, cells were exposed to increasing doses of gamma-irradiation (0-20 Gy) and HLA-G1 levels at the plasma membrane were analyzed at different times postirradiation by flow cytometry. HLA-G total expression and the presence of the Soluble form of HLA-G1 (sHLA-G1) in the culture medium of irradiated cells were also evaluated. IR was capable of downregulating cell surface and total HLA-G levels, with a concomitant increase of sHLA-G1 in the medium. These results could indicate that gamma-irradiation decreases HLA-G1 surface levels by enhancing the proteolytic cleavage of this molecule. (C) 2009 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
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页码:1010 / 1015
页数:6
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