Identification of secreted CD155 isoforms

被引:78
作者
Baury, W
Masson, D
McDermott, BM
Jarry, A
Blottière, HM
Blanchardie, P
Laboisse, CL
Lustenberger, P
Racaniello, VR
Denis, MG
机构
[1] Fac Med, INSERM, U539, F-44035 Nantes, France
[2] Columbia Univ, Coll Phys & Surg, Dept Microbiol, New York, NY 10032 USA
[3] Fac Med, Biochim Lab, F-44035 Nantes, France
关键词
CD155; poliovirus receptor; immunoglobulin superfamilly; soluble forms; splicing;
D O I
10.1016/S0006-291X(03)01560-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The CD155 gene is a member of the immunoglobulin superfamily. We first demonstrate the existence of soluble CD155 (sCD155) isoforms in culture medium conditioned by CD155-expressing cells, in human serum and in cerebrospinal fluid. sCD155 concentration was measured in human serum and cerebrospinal fluid using a specific ELISA. Analysis of conditioned media indicated that sCD155 release does not require protease activity. In order to determine which tissues are responsible for sCD155 expression, we have quantified CD 155 mRNAs in human normal tissues. The highest expression was observed in liver. The CD 155alpha transcript is the most abundant and the proportion of the CD155beta and CD155gamma variants was similar between the tissues. Finally, serum purified sCD155 reduces poliovirus entry mediated by membrane-bound CD155. The high level of CD 155 synthesis in many tissues and the presence of sCD155 in biological fluids suggest the existence of an important role for the protein in cellular function. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:175 / 182
页数:8
相关论文
共 36 条
[1]
Mouse homolog of poliovirus receptor-related gene 2 product, mPRR2, mediates homophilic cell aggregation [J].
Aoki, J ;
Koike, S ;
Asou, H ;
Ise, I ;
Suwa, H ;
Tanaka, T ;
Miyasaka, M ;
Nomoto, A .
EXPERIMENTAL CELL RESEARCH, 1997, 235 (02) :374-384
[2]
Shedding of kidney injury molecule-1, a putative adhesion protein involved in renal regeneration [J].
Bailly, V ;
Zhang, ZW ;
Meier, W ;
Cate, R ;
Sanicola, M ;
Bonventre, JV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (42) :39739-39748
[3]
Organization of the rat Tage4 gene and herpesvirus entry activity of the encoded protein [J].
Baury, B ;
Geraghty, RJ ;
Masson, D ;
Lustenberger, P ;
Spear, PG ;
Denis, MG .
GENE, 2001, 265 (1-2) :185-194
[4]
Secreted CEACAM1 splice variants in rat cell lines and in vivo in rat serum [J].
Budt, M ;
Michely, B ;
Müller, MM ;
Reutter, W ;
Lucka, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 292 (03) :749-755
[5]
CHADENEAU C, 1994, J BIOL CHEM, V269, P15601
[6]
The ectodomain of a novel member of the immunoglobulin subfamily related to the poliovirus receptor has the attributes of a bona fide receptor for herpes simplex virus types 1 and 2 in human cells [J].
Cocchi, F ;
Menotti, L ;
Mirandola, P ;
Lopez, M ;
Campadelli-Fiume, G .
JOURNAL OF VIROLOGY, 1998, 72 (12) :9992-10002
[7]
Denis MG, 1998, INT J ONCOL, V12, P997
[8]
THE HUMAN PRR2 GENE, RELATED TO THE HUMAN POLIOVIRUS RECEPTOR GENE (PVR), IS THE TRUE HOMOLOG OF THE MURINE MPH GENE [J].
EBERLE, F ;
DUBREUIL, P ;
MATTEI, MG ;
DEVILARD, E ;
LOPEZ, M .
GENE, 1995, 159 (02) :267-272
[9]
CEA-related cell adhesion molecule 1:: A potent angiogenic factor and a major effector of vascular endothelial growth factor [J].
Ergün, S ;
Kilic, N ;
Ziegeler, G ;
Hansen, A ;
Nollau, P ;
Götze, J ;
Wurmbach, JH ;
Horst, A ;
Weil, J ;
Fernando, M ;
Wagener, C .
MOLECULAR CELL, 2000, 5 (02) :311-320
[10]
Prominent role of the Ig-like V domain in trans-interactions of nectins -: Nectin3 and nectin4 bind to the predicted C-C′-C"-D β-strands of the nectin1 V domain [J].
Fabre, S ;
Reymond, N ;
Cocchi, F ;
Menotti, L ;
Dubreuil, P ;
Campadelli-Fiume, G ;
Lopez, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (30) :27006-27013