Identification of a novel family of cell-surface proteins expressed in human vascular endothelium

被引:144
作者
Yang, RB
Ng, CKD
Wasserman, SM
Colman, SD
Shenoy, S
Mehraban, F
Kömüves, LG
Tomlinson, JE
Topper, JN [1 ]
机构
[1] Millennium Pharmaceut Inc, Dept Cardiovasc Res, San Francisco, CA 94080 USA
[2] CuraGen Corp, Dept Collaborat Res, New Haven, CT 06511 USA
关键词
D O I
10.1074/jbc.M207410200
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
Vascular endothelial cells (EC) play a key role in a variety of pathophysiologic processes, such as angiogenesis, inflammation, cancer metastasis, and vascular diseases. As part of a strategy to identify all genes expressed in human EC, a full-length cDNA encoding a potential secreted protein harboring 10 epidermal growth factor (EGF)-like domains and one CUB domain at the carboxyl terminus (termed, SCUBE1 for Signal peptide-CUB-EGF-like domain containing protein 1) was identified. SCUBE1 shares homology with several protein families, including members of the fibrillin and Notch families, and the anticoagulant proteins, thrombomodulin and protein C. SCUBE1 mRNA is found in several highly vascularized tissues such as liver, kidney, lung, spleen, and brain and is selectively expressed in EC by in situ hybridization. SCUBE1 is a secreted glycoprotein that can form oligomers and manifests a stable association with the cell surface. A second gene encoding a homologue (designated SCUBE2) was also identified and is expressed in EC as well as other cell types. SCUBE2 is also a cell-surface protein and can form a heteromeric complex with SCUBE1. Both SCUBE1 and SCUBE2 are rapidly down-regulated in EC after interleukin-1beta and tumor necrosis factor-a treatment in vitro and after lipopolysaccharide injection in vivo. Thus, SCUBE1 and SCUBE2 define an emerging family of human secreted proteins that are expressed in vascular endothelium and may play important roles in development, inflammation, and thrombosis.
引用
收藏
页码:46364 / 46373
页数:10
相关论文
共 59 条
[1]
Steps toward mapping the human vasculature by phage display [J].
Arap, W ;
Kolonin, MG ;
Trepel, M ;
Lahdenranta, J ;
Cardó-Vila, M ;
Giordano, RJ ;
Mintz, PJ ;
Ardelt, PU ;
Yao, VJ ;
Vidal, CI ;
Chen, L ;
Flamm, A ;
Valtanen, H ;
Weavind, LM ;
Hicks, ME ;
Pollock, RE ;
Botz, GH ;
Bucana, CD ;
Koivunen, E ;
Cahill, D ;
Troncoso, P ;
Baggerly, KA ;
Pentz, RD ;
Do, KA ;
Logothetis, CJ ;
Pasqualini, R .
NATURE MEDICINE, 2002, 8 (02) :121-127
[2]
PDGF-D is a specific, protease-activated ligand for the PDGF β-receptor [J].
Bergsten, E ;
Uutela, M ;
Li, XR ;
Pietras, K ;
Östman, A ;
Heldin, CH ;
Alitalo, K ;
Eriksson, U .
NATURE CELL BIOLOGY, 2001, 3 (05) :512-516
[3]
Boehme MWJ, 1996, IMMUNOLOGY, V87, P134
[4]
THE CUB DOMAIN - A WIDESPREAD MODULE IN DEVELOPMENTALLY-REGULATED PROTEINS [J].
BORK, P ;
BECKMANN, G .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 231 (02) :539-545
[5]
Cines DB, 1998, BLOOD, V91, P3527
[6]
Clark TG, 1999, DEVELOPMENT, V126, P2631
[7]
CYTOKINES AND THEIR RECEPTOR COMPLEXES [J].
DAVIES, DR ;
WLODAWER, A .
FASEB JOURNAL, 1995, 9 (01) :50-56
[8]
DAVIS C G, 1990, New Biologist, V2, P410
[9]
STRUCTURAL-ANALYSIS OF THE UEGF GENE IN THE SEA-URCHIN STRONGYLOCENTROTUS-PURPURATUS REVEALS MORE SIMILARITY TO VERTEBRATE THAN TO INVERTEBRATE GENES WITH EGF-LIKE REPEATS [J].
DELGADILLOREYNOSO, MG ;
ROLLO, DR ;
HURSH, DA ;
RAFF, RA .
JOURNAL OF MOLECULAR EVOLUTION, 1989, 29 (04) :314-327
[10]
Inhibition of E-selectin gene expression by transforming growth factor β in endothelial cells involves coactivator integration of Smad and nuclear factor κB-mediated signals [J].
DiChiara, MR ;
Kiely, JM ;
Gimbrone, MA ;
Lee, ME ;
Perrella, MA ;
Topper, JN .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (05) :695-704