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作 者:赵红华[1] 林毓琴[1] 罗道春[1] 刘贤锡[1] 赵春华[1] 秦志杰[1]
机构地区:[1]山东医科大学生物化学教研室
出 处:《山东医科大学学报》1996年第3期181-185,共5页Acta Academiae Medicinae Shandong
基 金:国家自然科学基金
摘 要:收集正常的及良性前列腺增生症(BPH)的前列腺组织,用细胞培养、同位素掺入法分别测定各例标本的组织液对Swiss3T3细胞增殖的影响。结果表明,BPH组织液促细胞增殖效应为正常前列腺的5倍。正常前列腺组织用硫酸铵分级沉淀、肝素亲和层析、NaCl浓度梯度洗脱(收集1.3~1.7mol部分),分离纯化人前列腺生长因子(hPGF)。经SDS-PAGE鉴定达电泳纯,分子量约为17000,纯化约800倍。所得的hPGF对Swiss3T3细胞的增殖刺激作用呈现浓度依赖性。Recent studies have focused on the potential role of human prostatic growth factor(hPGF) in the pathogenesis of benign prostatic hyperplasia(BPH). Growth factors.as detected by DNA synthesis stimulating activity for Swiss 3T3 cells.in human normal prostates and BPH tissues were analyzed. Tissue extracts of both normal prostates and BPH significantly stimulated3 H-thymidine incorporation by Swiss 3T3 cells. The total content of growth factor(units per gram of tissue)in BPH was 5 times higher than those in normal prostates. hPGF was purified about 800-folds from alkaline homogenates of human normal prostates by a combination of ammonium sulfate precipitation and heparin affinity chromatography. The growth factor was eluted from the heparin-Sepharose column at 1.3~1. 7mol NaCl. hPGF in normal prostates and BPH tissues all stimulated DNA synthesis of Swiss 3T3 cells. The stimulation was concentration dependent. Furthermore ,BPH tissues contained a significantly greater amount of hPGF activity(units/mg protein) than normal prostates(P<0. 001 ). SDS-PAGE confirmed that the partially purified hPGF had a molecular weight of about 17KDa. These findings suggest that the increased hPGF biological activity might be responsible for the development of BPH.
分 类 号:R697.320.3[医药卫生—泌尿科学] R362[医药卫生—外科学]
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