过表达JHDM2A对猪iPSCs诱导效率的影响  

Effect of Overexpression of JHDM2A on iPSCs Induction Efficiency in Pigs

作　　者：任宣 宋延霞[1] 孙乐[1] 黄时海[2] 石德顺[1] 李湘萍[1] REN Xuan;SONG Yanxia;SUN Le;HUANG Shihai;SHI Deshun;LI Xiangping(State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources,Guangxi University,Nanning 530004,China;College of Life Science and Technology,Guangxi University,Nanning 530004,China)

机构地区：[1]广西大学,亚热带农业生物资源保护与利用国家重点实验室,南宁530004 [2]广西大学生命科学技术学院,南宁530004

出　　处：《中国畜牧兽医》2021年第12期4412-4421,共10页China Animal Husbandry & Veterinary Medicine

基　　金：国家自然科学基金(32060754);广西自然科学基金(2020GXNSFAA238039、2020GXNSFDA297009、2019GXSFDA185005)。

摘　　要：研究旨在探讨组蛋白赖氨酸去甲基化酶(JHDM2A)对猪成纤维细胞诱导为多能干细胞效率的影响,并对其内在的分子机制进行探究。以猪成纤维细胞为材料,采用多西环素(DOX)诱导的慢病毒生产诱导多能干细胞(iPSCs)体系,在此基础上过表达JHDM2A,通过碱性磷酸酶染色和绘制诱导时间轴检测其对诱导效率的影响;普通PCR技术检测克隆的多能性;免疫荧光检测多能因子的蛋白表达;实时荧光定量PCR检测JHDM2A在形成克隆后以及克隆分化过程中对多能因子、组蛋白甲基化相关基因表达的影响。结果表明,JHDM2A过表达组细胞在第3天发生形态变化,第8天形成iPSCs克隆,相比于对照组分别提前了1和2 d。碱性磷酸酶染色结果显示,与对照组相比,JHDM2A过表达组克隆形态明显改善,染色着色更深,诱导效率提高8倍。普通PCR结果显示,JHDM2A过表达组iPSCs、对照组iPSCs以及猪成纤维细胞(PFF)均表达内源性Oct4、Sox2、Klf4、c-Myc、Nanog,且iPSCs的Oct4表达量高于PFF。免疫荧光结果显示,JHDM2A过表达组iPSCs表达Oct4、Sox2、Stat3、JHDM2A,弱表达SSEA1、SSEA4。实时荧光定量PCR结果显示,与对照组和猪成纤维细胞相比,JHDM2A过表达组iPSCs的Sox2、Klf4、c-Myc、Nanog、Oct4、Tcl1的表达显著升高(P<0.05),Tfcp2l1和Zfp57的表达显著降低(P<0.05);JHDM2A过表达组P5代iPSCs培养基去除DOX后,随着代数的增加,Sox2、Nanog的表达逐渐降低,Klf4、c-Myc的表达先升高后降低,Oct4、Tcl1、Tfcp2l1、Zfp57的表达先降低后升高。以上结果表明,过表达JHDM2A通过促进组蛋白去甲基化提高猪成纤维细胞的诱导效率。The purpose of this study was to investigate the effect of histone demethylase(JHDM2A)on porcine fibroblast induced pluripotent stem cell efficiency,and to explore its intrinsic molecular mechanism.Porcine fibroblasts were used as materials,doxycycline(DOX)-inducible lentiviral vectors were used to produce iPSCs,and JHDM2A was overexpressed on this basis.The effect of JHDM2A on induction efficiency was detected by alkaline phosphatase(AP)staining and induction time axis.The pluripotency of the iPSCs was determined by PCR.The protein expression of the pluripotent factors was detected by immunofluorescence.The effects of JHDM2A on the expression of pluripotent factors and histone methylation related genes after clonies formation and during clonies differentiation were detected by Real-time quantitative PCR.The results showed that the cells of the JHDM2A overexpressed group deformed on the 3rd day and formed iPSCs clonies on the 8th day,which were 1 and 2 d earlier than those of control group.The results of AP staining showed that compared with the control group,the morphology of iPSCs in the JHDM2A overexpressed group was significantly improved,the AP staining was deeper,and the induction efficiency was increased by 8 times.Conventional PCR results showed that endogenous Oct4,Sox2,Klf4,c-Myc and Nanog were expressed in JHDM2A overexpressed group,control group and porcine fibroblasts(PFF),and the expression of Oct4 in iPSCs was higher than that in PFF.Immunofluorescence results showed that Oct4,Sox2,Stat3 and JHDM2A were expressed in iPSCs of JHDM2A overexpressed group,while SSEA1 and SSEA4 were weakly expressed.Real-time quantitative PCR results showed that compared with control group and PFF,the expressions of iPSCs genes Sox2,Klf4,c-Myc,Nanog,Oct4 and Tcl1 in JHDM2A overexpressed group were significantly increased(P<0.05),and the expressions of Tfcp2l1 and Zfp57 were significantly decreased(P<0.05).After DOX was removed from P5 iPSCs culture medium in the JHDM2A overexpressed group,with the increase of generation

关 键 词：猪 JHDM2A IPSCS 诱导效率 

分 类 号：S828[农业科学—畜牧学]