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作 者:余盼攀[1] 张胜初[1] 季世强[1] 苏龙丰[1] 张启瑜[1]
机构地区:[1]温州医学院附属第一医院肝胆外科,浙江温州325035
出 处:《温州医学院学报》2011年第6期511-514,共4页Journal of Wenzhou Medical College
基 金:浙江省外科学重中之重学科基金资助项目(2008-255)
摘 要:目的:建立一种合理、经济、便捷的大鼠原代肝星状细胞(hepatic stellate cells,HSC)分离方法。方法:运用改良肝脏原位灌注D-Hanks后,改用Ⅳ型胶原酶和DNA酶Ⅰ离体灌注,10%、16%Optiprep密度梯度离心分离大鼠肝星状细胞,台盼蓝排斥试验鉴定细胞活力,α-SMA免疫细胞化学法鉴定细胞纯度。结果:我们采用Optiprep密度梯度离心法成功分离出大鼠HSC,且活力、纯度均达到研究要求,HSC得率约为2×107/肝,细胞存活率为95%以上,纯度为90%以上。结论:本方法分离大鼠HSC合理、经济、便捷。Objective: To established a reasonable,ecnomic and convenient method of isolating hepatic stellate cells(HSC) in rats.Methods: The method for isolation of rat hepatic stellate cells was established with D-Hanks in situ liver recirculating perfusion and then isolated perfusion with Type IV collagenase and DNaseⅠand continuous density gradient centrifugation by 10%,16% Optiprep Solution.The viability of the isolated cells was deter-mined with trypan blue staining assay.The HSC were identified by immunocytochemical staining of α-SMA.Results: the rat HSC were successfully isolated and the viability and purity were reached the requirement.The average number of HSC from a single rat liver was 2×107,with viability over 95%,purity over 90%.Conclusion: This method for isolating HSC is reasonable,ecnomic and convenient.
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