| Project/Area Number |
10557165
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 展開研究 |
|---|
| Research Field |
Functional basic dentistry
|
|---|
| Research Institution | Okayama University |
|---|
Principal Investigator |
TAKIGAWA Masaharu Okayama University Dental School, Professor, 歯学部, 教授 (20112063)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
INOUE Miho Okayama University Dental School, Research Assistant, 歯学部, 教務員 (20271059)
HATTORI Takako Okayama University Dental School, Instructor, 歯学部, 助手 (00228488)
NAKANASHI Tohru Okayama University Dental School, Associate Professor, 歯学部, 助教授 (30243463)
TAMATANI Takuo Japan TABACOO Incorporation, Research Associate, 医薬基礎研究所, 主席研究員
|
|---|
| Project Period (FY) |
1998 – 1999
|
| Project Status |
Completed (Fiscal Year 1999)
|
| Budget Amount *help |
¥13,700,000 (Direct Cost: ¥13,700,000)
Fiscal Year 1999: ¥5,600,000 (Direct Cost: ¥5,600,000)
Fiscal Year 1998: ¥8,100,000 (Direct Cost: ¥8,100,000)
|
|---|
| Keywords | angiogenesis / connective tissue growth factor (CTGF) / anti-CTGF antibody / endothelial cells / metastasis / rheumatoid arthritis / neovascularization / myocardial infarction / 抗CTGF抗体 |
|---|
| Research Abstract |
1) As inhibitors for connective tissue growth factor (CTGF), a polyclonal antibody was raised by immunizing a synthesis CTGF fragment into rabbit. In addition, monoclonal anti-CTGF antibodies were also prepared.
2) Recombinant CTGF (rCTGF) promoted the adhesion, proliferation and migration of the vascular endothelial cells and these effects were inhibited by anti-CTGF antibody.
3) rCTGF markedly induced the tube formation of vascular endothelial cells, and this effect was stronger than that of basic fibroblast growth of vascular endothelial growth factor.
4) Application of rCTGF to the chicken chrioallantoic membrane (CAM) resulted in gross angiogenic response and the effect was inhibited by anti-CTGF antibody. rCTGF injected with collagen gels into the back of mice induced strong angiogenesis in vivo.
5) Among three cell lines (breast cancer cell line MDA231, fibrosarcoma cell line HT1080 and squamous carcinoma cell line A431), the ability to produce CTGF was highest in MDA231 and lowest in A431 and was parallel to their ability to form angiogenic tumors in nude mice. Anti-CTGF antibody inhibited tumor-induced angiogenesis in CAM.
6) CTGF was present in synovial fluid in patients with rheumatoid arthritis which is an angiogenic decease.
7) CTGF was expressed in the infarct zone of experimentally induced myocardial infarction in rats.
8) Human anti-CTGF antibodies were raised in transgenic mice producing human type antibody. One of them inhibited bone metastasis of MDA231 tumors which produce much CTGF.
These findings indicate that CTGF is a novel, potent angiogenesis factor which functions in multi-stages in physiological and pathological angiogenesis and suggest that anti-CTGF antibody can be used as an inhibitor for angiogenesis.
|
