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bFGF调节PDGF对人成骨细胞的促增殖作用
引用本文:Chen J,Yang D,Jing Z,Wu D,Ding H,Jin D. bFGF调节PDGF对人成骨细胞的促增殖作用[J]. 中华外科杂志, 2000, 38(9): 707-710,I039
作者姓名:Chen J  Yang D  Jing Z  Wu D  Ding H  Jin D
作者单位:第一军医大学南方医院骨科,广州
基金项目:国家自然科学基金!(395 0 0 175 )
摘    要:目的 探讨碱性成纤维细胞生长因子(bFGF)对血小板衍生生长因子(PDGF)促成骨细胞增殖作用的影响及其机制。方法 分离培养人成骨细胞;以PDGF-AB(100ng/ml)单独培养、bFGF(10ng/ml)与PDGF-AB(100ng/ml)混合培养、不加生长因子等3种方式培养细胞,绘制细胞生长曲线;bFGF(10ng/ml)与PDGF-AA或PDGF-BB(浓度均为40ng/ml)以不同方式联

关 键 词:血小板源生长因子 碱性成纤维细胞生长因子

Mitogenesis of platelet-derived growth factors to human osteoblasts modulated by basic fibroblast growth factor
Chen J,Yang D,Jing Z,Wu D,Ding H,Jin D. Mitogenesis of platelet-derived growth factors to human osteoblasts modulated by basic fibroblast growth factor[J]. Chinese Journal of Surgery, 2000, 38(9): 707-710,I039
Authors:Chen J  Yang D  Jing Z  Wu D  Ding H  Jin D
Affiliation:Department of Orthopeadic Surgery, Nanfang Hospital, First Military Medical University, Guangzhou 510515, China.
Abstract:OBJECTIVES: To investigate the mechanism by which basic fibroblast growth factor modulates the mitogenesis of platelet-derived growth factor to human osteoblasts. METHODS: The osteoblasts isolated from human fetal calvaria were incubated with PDGF-AB (100 ng/ml) or bFGF(10 ng/ml) combined with PDGF-AB (100 ng/ml); the growth curve was plotted. The(3)H-TdR incorporation of the osteoblasts was measured after the cells were incubated with different combination of bFGF and PDGF-AA or PDGF-BB. After incubated with bFGF (10 ng/ml) for 24 hours, the number of PDGFR-alpha and PDGFR-beta on the membrane of the osteoblasts was detected by fluoroimmunoassay. RESULTS: Four days after PDGF-AB added into the medium, the population of the osteoblasts was larger than that of the control (P < 0.05). The number of the osteoblasts incubated with PDGF-AB (12.1 x 10(4)) was 1.8 times as large as the control (6.8 x 10(4)) in the 10th day (P < 0.05), and that of the osteoblasts incubated with both bFGF and PDGF-AB increased more quickly than the cells only incubated with PDGF-AB. The incorporation of (3)H-TdR into the osteoblasts cultured with bFGF combined with PDGF-AA (533.6 +/- 13.1) was more than that cultured only with PDGF-AA (435.4 +/- 14.8, P < 0.01), so was the incorporation of (3)H-TdR of those cells cultured with bFGF and then PDGF-AA (633.8 +/- 51.5). bFGF upregulated PDGFR-alpha and downregulated PDGFR-beta on the surface of the human osteoblasts. CONCLUSION: bFGF elevates the mitogenesis of PDGF-AA or -AB to human osteoblasts by upregulating PDGFR-alpha.
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