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类淀粉样前体蛋白2与HLA I类分子的关联。

Amyloid precursor-like protein 2 association with HLA class I molecules.

作者信息

Tuli Amit, Sharma Mahak, Wang Xiaojian, Simone Laura C, Capek Haley L, Cate Steven, Hildebrand William H, Naslavsky Naava, Caplan Steve, Solheim Joyce C

机构信息

Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Cancer Immunol Immunother. 2009 Sep;58(9):1419-31. doi: 10.1007/s00262-009-0657-z. Epub 2009 Jan 31.

Abstract

Amyloid precursor-like protein 2 (APLP2) is a ubiquitously expressed protein. The previously demonstrated functions for APLP2 include binding to the mouse major histocompatibility complex (MHC) class I molecule H-2K(d) and down regulating its cell surface expression. In this study, we have investigated the interaction of APLP2 with the human leukocyte antigen (HLA) class I molecule in human tumor cell lines. APLP2 was readily detected in pancreatic, breast, and prostate tumor lines, although it was found only in very low amounts in lymphoma cell lines. In a pancreatic tumor cell line, HLA class I was extensively co-localized with APLP2 in vesicular compartments following endocytosis of HLA class I molecules. In pancreatic, breast, and prostate tumor lines, APLP2 was bound to the HLA class I molecule. APLP2 was found to bind to HLA-A24, and more strongly to HLA-A2. Increased expression of APLP2 resulted in reduced surface expression of HLA-A2 and HLA-A24. Overall, these studies demonstrate that APLP2 binds to the HLA class I molecule, co-localizes with it in intracellular vesicles, and reduces the level of HLA class I molecule cell surface expression.

摘要

淀粉样前体样蛋白2(APLP2)是一种广泛表达的蛋白质。先前已证明APLP2的功能包括与小鼠主要组织相容性复合体(MHC)I类分子H-2K(d)结合并下调其细胞表面表达。在本研究中,我们研究了APLP2与人肿瘤细胞系中人类白细胞抗原(HLA)I类分子的相互作用。在胰腺、乳腺和前列腺肿瘤细胞系中很容易检测到APLP2,尽管在淋巴瘤细胞系中仅发现极少量的APLP2。在胰腺肿瘤细胞系中,HLA I类分子内吞后,HLA I类与APLP2在囊泡区室中广泛共定位。在胰腺、乳腺和前列腺肿瘤细胞系中,APLP2与HLA I类分子结合。发现APLP2与HLA-A24结合,且与HLA-A2的结合更强。APLP2表达增加导致HLA-A2和HLA-A24的表面表达减少。总体而言,这些研究表明APLP2与HLA I类分子结合,在细胞内囊泡中与其共定位,并降低HLA I类分子细胞表面表达水平。

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