Gene therapy for temporomandibular joint osteoarthritis
Gene therapy for temporomandibular joint osteoarthritis
批准号:
12557169
负责人:
KUBOKI Takuo
金额:
$7.68万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2002
中文摘要
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英文摘要
The purposes of this research are to clarify the mechanism of cartilage degradation in osteoarthritis (OA) and to investigate the possibility of gene therapy for articular cartlige restoration using connective tissue growth fector (CTGF).First, we establish a genuine mechanical-stress-induced OA model of the rabbit TMJ. In the experimental rabbits, repetitive forced jaw opening (RFJO) 3 hours/day for 5 days was applied. By histological assessment of the TMJ articular tissues, partial eburnation of the articular cartilage, reactive marginal proliferation of the articular cartilage chondrocytes and nested proliferation of chondrocytes in the subchondral bone area were observed at 7 days after the RFJO period. These results suggest the RFJO protocol without any surgical intervention can induce evident OA-like lesions in the rabbit TMJ, and this OA model may greatly contribute to the elucidation of the cartilage degradation mechanism in TMJ OA.Second, we investigated the effects of CTGF/Hcs24 transduced by recombinant adenoviruses on the rabbit articular cartilage (RAC) cells in vitro. When RAC cells were infected with adenoviruses caontaining the CTGF/Hcs24 gene, RAC cells expressed CTGF/Hcs24 mRNA and produced CTGF/Hcs24 protein. RAC cells synthesized more proteoglycan than the control cells.
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T Kuboki et al.: "Soluble tumor necrosis factor receptors are up-regulated in synovial fluids from osteoarthritic temporomandibular joints"Archs Oral Biol. (in press). (2003)
T Kuboki 等人:“骨关节炎颞下颌关节滑液中可溶性肿瘤坏死因子受体上调”Archs Oral Biol。
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T.Kuboki et al.: "CTGF/Hcs24, a hypertrophic chondrocytes specific gene product, stimulates proliferation and differentiation, but not hypertrophy of cultured articular chondrocytes"J Cellular Physiol.. 192. 55-63 (2002)
T.Kuboki 等人:“CTGF/Hcs24,一种肥大软骨细胞特异性基因产物,刺激增殖和分化,但不刺激培养的关节软骨细胞肥大”J Cellular Physiol.. 192. 55-63 (2002)
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T. Nishida, S. Kubota, T. Nakanishi, T. Kuboki, G. Yoshimichi, S. Kondo, M. Takigawa: "CTGF/Hcs24, a hypertrpphic chondrocytes specific gene product, stimulates proliferation and differentiation, but not hypertrophy of cultured articular chondrocytes"J Ce
T. Nishida、S. Kubota、T. Nakanishi、T. Kuboki、G. Yoshimichi、S. Kondo、M. Takikawa:“CTGF/Hcs24 是一种肥大软骨细胞特异性基因产物,可刺激增殖和分化,但不会刺激培养的软骨细胞肥大。
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J. Uehara, T. Kuboki, T. Fujisawa, S. Kojima, K. Maekawa, H. Yatani: "Soluble tumor necrosis factor receptors are up-regulated in synovial fluids from osteoarthritic temporomandibular joints, preliminarily accepted"Archs Oral Biol.. (2003)
J. Uehara、T. Kuboki、T. Fujisawa、S. Kojima、K. Maekawa、H. Yatani:“骨关节炎颞下颌关节滑液中可溶性肿瘤坏死因子受体上调,初步接受”Archs Oral Biol..
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完山学 ほか: "アデノウイルスベクターによる培養骨芽細胞と骨組織への結合組織成長因子の遺伝子導入"日本補綴歯科学会雑誌. 44(104). 196 (2000)
Manabu Kanzan 等人:“使用腺病毒载体将结缔组织生长因子基因转移到培养的成骨细胞和骨组织中”,日本修复医学会杂志 44(104)。
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