Connective tissue growth factor induces the proliferation, migration, and tube formation of vascular endothelial cells in vitro, and angiogenesis in vivo

被引:355
作者
Shimo, T
Nakanishi, T
Nishida, T
Asano, R
Kanyama, M
Kuboki, T
Tamatani, T
Tezuka, K
Takemura, M
Matsumura, T
Takigawa, M [1 ]
机构
[1] Okayama Univ, Sch Dent, Dept Biochem & Mol Dent, Okayama 7008525, Japan
[2] Okayama Univ, Sch Dent, Biodent Res Ctr, Okayama 7008525, Japan
[3] Okayama Univ, Sch Dent, Dept Oral & Maxillofacial Surg 2, Okayama 7008525, Japan
[4] Okayama Univ, Sch Dent, Dept Fixed Prosthodont, Okayama 7008525, Japan
[5] Japan Tobacco Inc, Pharmaceut Frontier Res Labs, Yokohama, Kanagawa 2360004, Japan
[6] Osaka Univ, Fac Dent, Dept Oral Anat, Osaka 5650871, Japan
关键词
angiogenesis; connective tissue growth factor (CTGF); endothelial cells; hypertrophic chondrocytes; neovascularization;
D O I
10.1093/oxfordjournals.jbchem.a022414
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
Connective tissue growth factor (CTGF) is a novel cysteine-rich, secreted protein. Recently, we found that inhibition of the endogenous expression of CTGF by its antisense oligonucleotide and antisense RNA suppresses the proliferation and migration of vascular endothelial cells. In the present study, the following observations demonstrated the angiogenic function of CTGF in vitro and in vivo: (i) purified recombinant CTGF (rCTGF) promoted the adhesion, proliferation and migration of vascular endothelial cells in a dose-dependent manner under serum-free conditions, and these effects were inhibited by anti-CTGF antibodies; (ii) rCTGF markedly induced the tube formation of vascular endothelial cells, and this effect was stronger than that of basic fibroblast growth factor or vascular endothelial growth factor; (iii) application of rCTGF to the chicken chorioallantoic membrane resulted in a gross angiogenic response, and this effect was also inhibited by anti-CTGF antibodies, (iv) rCTGF injected with collagen gel into the backs of mice induced strong angiogenesis in vivo. These findings indicate that CTGF is a novel, potent angiogenesis factor which functions in multi-stages in this process.
引用
收藏
页码:137 / 145
页数:9
相关论文
共 44 条
[1]   CYR61, a product of a growth factor-inducible immediate early gene, promotes angiogenesis and tumor growth [J].
Babic, AM ;
Kireeva, ML ;
Kolesnikova, TV ;
Lau, LF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) :6355-6360
[2]   THE MODULAR ARCHITECTURE OF A NEW FAMILY OF GROWTH-REGULATORS RELATED TO CONNECTIVE-TISSUE GROWTH-FACTOR [J].
BORK, P .
FEBS LETTERS, 1993, 327 (02) :125-130
[3]   CONNECTIVE-TISSUE GROWTH-FACTOR - A CYSTEINE-RICH MITOGEN SECRETED BY HUMAN VASCULAR ENDOTHELIAL-CELLS IS RELATED TO THE SRC-INDUCED IMMEDIATE EARLY GENE-PRODUCT CEF-10 [J].
BRADHAM, DM ;
IGARASHI, A ;
POTTER, RL ;
GROTENDORST, GR .
JOURNAL OF CELL BIOLOGY, 1991, 114 (06) :1285-1294
[4]   EFFECTS OF TUMOR NECROSIS FACTOR-ALPHA ON PROLIFERATION AND EXPRESSION OF DIFFERENTIATED PHENOTYPES IN RABBIT COSTAL CHONDROCYTES IN CULTURE [J].
ENOMOTO, M ;
PAN, HO ;
KINOSHITA, A ;
YUTANI, Y ;
SUZUKI, F ;
TAKIGAWA, M .
CALCIFIED TISSUE INTERNATIONAL, 1990, 47 (03) :145-151
[5]  
ENOMOTO M, 1992, BIOL REGULATION CHON, P321
[6]  
FOLKMAN J, 1986, CANCER RES, V46, P467
[7]   Blood vessel formation: What is its molecular basis? [J].
Folkman, J ;
DAmore, PA .
CELL, 1996, 87 (07) :1153-1155
[8]   Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis [J].
Hanahan, D ;
Folkman, J .
CELL, 1996, 86 (03) :353-364
[9]   Endothelial Cells Synthesize Basic Fibroblast Growth Factor and Transforming Growth Factor Beta [J].
Hannan, Robert L. ;
Kourembanas, Stella ;
Flanders, Kathleen C. ;
Rogelj, Snezna J. ;
Roberts, Anita B. ;
Faller, Douglas V. ;
Klagsbrun, Michael .
GROWTH FACTORS, 1988, 1 (01) :7-17
[10]   SIGNIFICANT CORRELATION BETWEEN CONNECTIVE-TISSUE GROWTH-FACTOR GENE-EXPRESSION AND SKIN SCLEROSIS IN TISSUE-SECTIONS FROM PATIENTS WITH SYSTEMIC-SCLEROSIS [J].
IGARASHI, A ;
NASHIRO, K ;
KIKUCHI, K ;
SATO, S ;
IHN, H ;
GROTENDORST, GR ;
TAKEHARA, K .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 105 (02) :280-284