摘要
目的 :测定猪血小板衍生生长因子的相对分子质量和纯度并观察其对培养的人血管内皮细胞 DNA合成的影响。方法 :用高效液相色谱凝胶过滤柱 ,标准蛋白制备标准曲线 ,测定猪血小板衍生生长因子的相对分子质量和纯度 ;采用培养的人脐静脉血管内皮细胞 ,应用 3H- Td R掺入的方法 ,观察猪血小板衍生生长因子对血管内皮细胞 DNA合成的影响。 结果 :测得的猪血小板衍生生长因子的相对分子质量为 2 912 0 ,纯度为 89.46 % ;猪血小板衍生生长因子可促进处于静止状态的人血管内皮细胞 DNA的合成 ,在 40 ng/ ml的质量浓度时 DNA的合成最为明显 ,且于血小板衍生生长因子作用 48h时合成最为显著。 结论 :猪血小板衍生生长因子的相对分子质量为 2 912 0 ,可明显促进培养的血管内皮细胞
Objective: To determine the molecular weight and purity of porcine platelet derived growth factor (pPDGF) and to investigate its effect on DNA synthesis of human umbilical vein endothelial cells. Methods: In the present experiment, the high performance liquid chromatography was used and the molecular weight and purity of pPDGF were studied. Human umbilical vein endothelial cells was cultured and effects of pPDGF on DNA synthesis of endothelial cells was observed by 3H TdR incorporation in vitro . Results: The findings of high performance liquid chromatography showed that the molecular weight of pPDGF was 29 120 and the purity was 89.46%, and pPDGF significantly promoted DNA synthesis of quiescent endothelial cells with a maximal response at a concentration of 40 ng/ml at 48 h. Conclusion: The molecular weight of pPDGF is 29 120, and it can promote DNA synthesis of cultured human umbilical vein endothelial cells. [
出处
《第二军医大学学报》
CAS
CSCD
北大核心
2001年第2期155-158,共4页
Academic Journal of Second Military Medical University