The recombinant lectin-like domain of thrombomodulin inhibits angiogenesis through interaction with Lewis Y antigen

被引：46

作者：

Kuo, Cheng-Hsiang ^{[1
,2
,3
]}

Chen, Po-Ku ^{[1
,2
,3
]}

Chang, Bi-Ing ^{[1
,3
]}

Sung, Meng-Chen ^{[1
]}

Shi, Chung-Sheng ^{[1
]}

Lee, Jeng-Shin ^{[4
]}

Chang, Chuan-Fa ^{[3
,5
]}

Shi, Guey-Yueh ^{[1
,3
]}

Wu, Hua-Lin ^{[1
,3
,6
]}

机构：

[1] Natl Cheng Kung Univ, Coll Med, Dept Biochem & Mol Biol, Tainan 701, Taiwan

[2] Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 701, Taiwan

[3] Natl Cheng Kung Univ, Coll Med, Cardiovasc Res Ctr, Tainan 701, Taiwan

[4] Harvard Univ, Sch Med, Harvard Gene Therapy Initiat, Boston, MA USA

[5] Natl Cheng Kung Univ, Coll Med, Dept Med Lab Sci & Biotechnol, Tainan 701, Taiwan

[6] Natl Cheng Kung Univ, Ctr Biosci & Biotechnol, Tainan 701, Taiwan

来源：

BLOOD | 2012年 / 119卷 / 05期

关键词：

SOLUBLE THROMBOMODULIN; PLASMA THROMBOMODULIN; MITOGENIC ACTIVITY; GROWTH; EXPRESSION; PROTEIN; METASTASIS; ADHESION; BINDING; INVOLVEMENT;

D O I：

10.1182/blood-2011-08-376038

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Lewis YAg (LeY) is a cell-surface tetrasaccharide that participates in angiogenesis. Recently, we demonstrated that LeY is a specific ligand of the recombinant lectin-like domain of thrombomodulin (TM). However, the biologic function of interaction between LeY and TM in endothelial cells has never been investigated. Therefore, the role of LeY in tube formation and the role of the recombinant lectin-like domain of TM-TM domain 1 (rTMD1)-in antiangiogenesis were investigated. The recombinant TM ectodomain exhibited lower angiogenic activity than did the recombinant TM domains 2 and 3. rTMD1 interacted with soluble LeY and membrane-bound LeY and inhibited soluble LeY-mediated chemotaxis of endothelial cells. LeY was highly expressed on membrane ruffles and protrusions during tube formation on Matrigel. Blockade of LeY with rTMD1 or Ab against LeY inhibited endothelial tube formation in vitro. Epidermal growth factor (EGF) receptor in HU-VECs was LeY modified. rTMD1 inhibited EGF receptor signaling, chemotaxis, and tube formation in vitro, and EGF-mediated angiogenesis and tumor angiogenesis in vivo. We concluded that LeY is involved in vascular endothelial tube formation and rTMD1 inhibits angiogenesis via interaction with LeY. Administration of rTMD1 or recombinant adeno-associated virus vector carrying TMD1 could be a promising antiangiogenesis strategy. (Blood. 2012;119(5): 1302-1313)

引用

页码：1302 / 1313

页数：12

共 48 条

[1] The N-terminal domain of thrombomodulin sequesters high-mobility group-B1 protein, a novel antiinflammatory mechanism [J].