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.
引用
收藏
页码:1010 / 1015
页数:6
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