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ID:31081410
大小:1.73 MB
页数:9页
时间:2019-01-06
《胎鼠肺泡ⅱ型上皮细胞的分离及原代培养》由会员上传分享,免费在线阅读,更多相关内容在工程资料-天天文库。
1、胎鼠肺泡Ⅱ型上皮细胞的分离及原代培养付红敏,许峰,黄波,杨鸣,符跃强,方芳,匡凤梧(重庆医科大学儿童医院PICU,重庆400014)摘要:目的探讨胎鼠肺泡Ⅱ型上皮细胞(AECⅡ)的分离、纯化及原代培养方法,为有关胎儿肺发育及新生儿肺部疾病的研究奠定基础。方法采用胰酶结合胶原酶的消化方法,分离肺组织细胞成份,然后经差速离心和差速贴壁的方法纯化AECⅡ,进行原代培养;通过台盼蓝染色检测细胞活力,倒置相差显微镜观察细胞生长特点及形态特征,透射电镜鉴定,改良巴氏染色检测细胞纯度以及免疫荧光技术检测表面蛋白C(SPC)的表达。结果每3~5只胎鼠可获得AECⅡ(36±5)
2、×106,活力(98±2)%。镜下观察原代AECⅡ呈岛状生长,外观呈多边形或立方形。透射电镜可见特征性的板层小体,改良巴氏染色见胞质内有较多颗粒,纯度为(96±3)%,呈现SPC绿色免疫荧光的细胞占96%以上。结论利用胰酶和胶原酶消化,以及差速离心和差速贴壁的方法可成功分离出高产量、高纯度的胎鼠AECⅡ,能满足体外进一步实验的需要。关键词:胎鼠;肺泡Ⅱ型上皮细胞;原代培养;分离中图分类号:R714.5;R714.7;Q813.1IsolationandprimarycultureoftypeⅡalveolarepithelialcellsfromfetalra
3、tlungFUHong-min,XUFeng,HUANGBo,YANGmin,FUyueqiang,FANGFang,KUANGFeng-wu.PediatricsIntensiveCareUnit,Children’sHospital,ChongqingUniversityofMedicalSciences,Chongqing400014,China【Abstract】ObjectiveTodeveloptheisolationandpurificationtechnologyfortypeⅡalveolarepithelialcells(AECⅡ)offe
4、talrat,thusprovidingexperimentalmeansforthe基金项目:国家自然科学基金面上项目(基金号:30670931)NationalNaturalScienceFoundation(NO.30670931)高等学校博士学科点专项科研基金项目(基金号:20070631010)ResearchFundfortheDoctoralProgramofHigherEducation(NO.200706310109)studyoflungdevelopmentorneonatallungdisease.MethodsLungtissueso
5、f19-dayfetalratsweredigestedwithtrypsinandcollagenase,thenpurifiedforAECⅡwithdifferentcentrifugalforceandrepeatedattachment.Cellviabilitywasevaluatedbytypraninclusiondyingbeforeplatingintosix-wellflask.Growthstatusandshapeofattachedcellswereobservedwithinvertedphasecontrastmicroscop
6、e.AECⅡwereidentifiedbyelectronmicroscopeanditspercentagewasassessedbymodifiedPapanicolaoudyingandimmunofluorescence,thelatteraimingtodetectexpressionofsurfactantproteinC(SPC)inAECⅡ.ResultsThetotalamountofcellsweharvestedfrom3to5fetalratwas(36±5)×106withaviabilityof(98±2)%.Cellswerel
7、ikepolygonalandconnectedlikeislandundermicroscope.AECⅡwasascertainedbylamellarbodiesfoundincytoplasmaunderelectronmicroscopeanditspercentagewas(96±3)%identifiedbymodifiedPapanicolaoudying,thesameastheresultbyimmunofluorescenceforSPC.ConclusionHighlyPurifiedandviableAECⅡcouldbeachiev
8、edbyourmethodsandth
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