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作 者:邱志东[1] 缪辉来[1] 张晟晃[1] 陈念平[1] 陈明[1] 郑淑华[2]
机构地区:[1]广东医学院附属医院肝胆外科,广东省湛江524001 [2]广东医学院肝胆外科研究室
出 处:《中国基层医药》2009年第5期769-771,共3页Chinese Journal of Primary Medicine and Pharmacy
基 金:广东省社会发展领域科技计划项目(20053026),广东省湛江市科技招标项目基金资助(200515)
摘 要:目的探讨肝细胞生长因子(HGF)与酸性成纤维细胞生长因子(aFGF)体外诱导胚胎肝干细胞抗原阳性(Sca-1^+)细胞向肝细胞或肝细胞前体分化的可行性。方法免疫磁珠分离法分离Sca-1^+细胞,相差显微镜观察细胞形态,(RT-PCR半定量逆转录聚合酶链反应)法检测细胞自蛋白(ALB)、转甲状腺蛋白mRNA水平表达;免疫组织化学法检测ALB、AFP和CKS/18蛋白水平的表达,以及检测细胞糖原染色和尿素合成功能。结果分离后Sca-1^+细胞活力为(94.24±1.04)%,纯度为(85.57±1.66)%,回收率为(62.31±1.85)%。Sca-1^+细胞经HGF和aFGF诱导分化后,细胞形态变成不规则,明显向肝细胞变化,AFP蛋白表达消失、ALB和CK8/18蛋白表达升高,ALB、转甲状腺蛋白mRNA表达升高,且细胞糖原染色和尿素合成功能增强,逐渐向成熟肝细胞转化。结论HGF与aFGF可在体外诱导胚胎肝Sca-1^+细胞向肝细胞或肝细胞前体分化。Objective To investigate the feasbility of the orient differentiation from embryo hepatic Sca-1^ + cell to hepatic cell or hepatic cell precursor under the induction of hepatocyte growth factor(HGF) and acor fibroblast growth factor(aFGF) in vitro. Methods Sca-1^ + cells were isolated by immunomagnetic beads and their morphous were observed by contrast phase microscope. The expression of mRNA of albumin(ALB) and meta-thyroprotein were detected by RT-PCR;ALB, AFP, CK8/18 protein were detected by immunohistochemical method, and cell staining for glycogen and urea synthesis function were tested. Results The activity, purity, recovery rate of Sca-1^+ cells were (94. 24 ± 1.04) %, ( 85.57 ± 1.66) %, ( 62. 31 ±1.85 ) % respectively. After the induction of HGF and aFGF, Sca- 1 ^+ cells became anomalism and transformed to heptic cell in morphous, disappeared in expression of AFP protein and upregulated in expression of ALB and CK8/18 protein, upregulated in expression of ALB and transthyroprotein mRNA, cell staining of glycogen and urea synthesis function were strengthened, the cell differentiated to mature hepatic cell. Conclusion Embryo hepatic Sca-1^ + cell could differentiate to hepatic cell or hepatic cell precursor under the induction of HGF and aFGF in vitro.
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