Membrane topography of HLA I, HLA II, and ICAM-1 is affected by IFN-γ in lipid rafts of uveal melanomas

被引:20
作者
Bene, L
Bodnár, A
Damjanovich, S [1 ]
Vámosi, G
Bacsó, Z
Aradi, E
Berta, A
Damjanovich, J
机构
[1] Univ Debrecen, Med & Hlth Sci Ctr, Res Ctr Mol Med, Dept Biophys & Cell Biol, H-4012 Debrecen, Hungary
[2] Univ Debrecen, Med & Hlth Sci Ctr, Res Ctr Mol Med, Hungarian Acad Sci,Cell Biophys Res Grp, H-4012 Debrecen, Hungary
[3] Univ Debrecen, Med & Hlth Sci Ctr, Res Ctr Mol Med, Dept Biochem & Mol Biol, H-4012 Debrecen, Hungary
[4] Univ Debrecen, Med & Hlth Sci Ctr, Dept Ophthalmol, H-4012 Debrecen, Hungary
基金
匈牙利科学研究基金会;
关键词
uveal melanoma; HLA I and II; ICAM-1; protein pattern; lipid raft; fluorescence resonance energy transfer; flow cytometry; confocal laser scanning microscopy;
D O I
10.1016/j.bbrc.2004.07.171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lateral distribution and colocalization of HLA I, HLA-DR, and ICAM-1 proteins was studied for the first time in the plasma membrane of two human uveal melanoma cell lines, OCM-1 and OCM-3. Our fluorescence resonance energy transfer and confocal laser scanning microscopic experiments revealed that these molecules are mostly confined to the same membrane regions, where they form similar protein patterns (homo- and hetero-associates) to those found previously on other cell types of lymphoid as well as colorectal carcinoma origin. Confocal microscopic colocalization experiments with GM(1) gangliosides and the GPI-anchored CD59 molecules showed enrichment of HLA I, HLA-DR, and ICAM-1 molecules in specific membrane domains (lipid rafts) excluding the transferrin receptor. IFN-gamma remarkably increased the expression levels of these molecules and rearranged their association patterns, which can affect the adoptive immune response of effector cells. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:678 / 683
页数:6
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