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The Potential of Rat Inner Cell Mass and Fetal Neural Stem Cells to Generate Chimeras
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作者 郭继彤 李雪峰 +6 位作者 Shahnaz Fida 苟克勉 Nakisa Malakooti ZHANG Chun-fang John R Morrison Alan O Trounson DU Zhong-tao 《Zoological Research》 CAS CSCD 北大核心 2009年第2期158-164,共7页
The rat chimera is an important animal model for the study of complex human diseases. In the present study we evaluated the chimeric potential of rat inner cell masses (ICMs) and fetal neural stem (FNS) cells. In ... The rat chimera is an important animal model for the study of complex human diseases. In the present study we evaluated the chimeric potential of rat inner cell masses (ICMs) and fetal neural stem (FNS) cells. In result, three rat chimeras were produced by day 5 (D5) Sprague-Dawley (SD) blastocysts injected with ICMs derived from day 6 (D6) and D5 Dark Agouti (DA) blastocysts; four rat chimeras had been generated by D5 DA blastocyst injected with D5 SD ICMs. For the requirement of gene modification, cultured rat inner cell mass cells were assessed to produce chimeras, but no chimeras were generated from injected embryos. The potential to generate chimeras from rFNS and transfected rFNS cells were tested, but no chimeric pups were produced. Only 2 of 41 fetuses derived from D5 DA blastocyst injection with SD LacZ transfected rFNS cells showed very low number of LacZ positive cells in the section. These results indicate that DA and SD rat ICMs arc able to contribute to chimeras, but their potential decreases significantly after culture in vitro (P〈0.05), and rFNS cells only have the potential to contribute to early fetal development. 展开更多
关键词 rat chimeras Inner cell mass rat fetal neural stem cells Blastocyst injection
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用大鼠心肌条件培养基建立来源于C57BL/6J小鼠的ES细胞系 被引量:8
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作者 童英 邹冀中 尚克刚 《北京大学学报(自然科学版)》 CAS CSCD 北大核心 2000年第4期472-476,共5页
报道一种新的建立C57BL/ 6J小鼠ES细胞系的方法。采用大鼠心肌条件培养基 ,在不使用饲养层细胞和白血病抑制因子 (LIF)的情况下 ,从C57BL/ 6J品系小鼠中建成 1个ES细胞系即MESPU 4 1,成系率为 1 0 %。MESPU 4 1细胞为XX型 ,核型正常率高... 报道一种新的建立C57BL/ 6J小鼠ES细胞系的方法。采用大鼠心肌条件培养基 ,在不使用饲养层细胞和白血病抑制因子 (LIF)的情况下 ,从C57BL/ 6J品系小鼠中建成 1个ES细胞系即MESPU 4 1,成系率为 1 0 %。MESPU 4 1细胞为XX型 ,核型正常率高达 89% ,表现出XX型ES细胞系少有的稳定性。进行体内分化实验时MESPU 4 1细胞能发生广泛分化形成畸胎瘤。嵌合体制作实验证实MESPU 4 1细胞具有嵌合能力 ,能参与胚胎的发育。采用RT PCR方法 ,检测出大鼠心肌细胞有LIFmRNA的表达 ,这可能与其条件培养基保持ES细胞未分化状态并使X染色体稳定有关。同时 ,还对大鼠心肌细胞进行了永生化的尝试 ,共得到了 4个永生化克隆 ,这将进一步简化ES细胞建系和培养工作 ,为进一步研究ES细胞在体外培养过程中的稳定性开创了新的起点。 展开更多
关键词 ES细胞系 小鼠品系 大鼠心肌条件培养基
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骨髓间充质干细胞参与牙髓损伤修复的体内实验研究 被引量:1
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作者 郝靖惠 杨博 +3 位作者 白庆霞 张艳 刘晓静 陆群 《牙体牙髓牙周病学杂志》 CAS 北大核心 2012年第4期189-193,218,共6页
目的:观察体内的骨髓间充质干细胞(BMMSCs)能否参与牙髓损伤的局部修复,初步探讨骨髓间充质干细胞在牙髓损伤修复中的作用。方法:构建绿色荧光蛋白转基因大鼠骨髓间充质干细胞(GFP-BMMSCs)嵌合SD大鼠模型,30 d后,通过流式细胞术检测外... 目的:观察体内的骨髓间充质干细胞(BMMSCs)能否参与牙髓损伤的局部修复,初步探讨骨髓间充质干细胞在牙髓损伤修复中的作用。方法:构建绿色荧光蛋白转基因大鼠骨髓间充质干细胞(GFP-BMMSCs)嵌合SD大鼠模型,30 d后,通过流式细胞术检测外周血单核细胞和骨髓间充质干细胞中荧光细胞的比例,冰冻切片观察心、肝、肾组织中是否有荧光细胞的分布,检测模型是否构建成功。然后利用该模型,通过制备牙本质缺损构建牙髓损伤模型,分别于牙本质缺损后5、10、15 d取材,切片,HE及免疫荧光染色,观察牙髓的病理变化以及GFP-BMMSCs在牙髓组织中的分布情况和变化。结果:HE染色可见牙本质缺损组初期有牙髓充血,后期牙髓炎症逐渐恢复并有修复性牙本质形成。免疫荧光染色可见牙髓组织中有荧光细胞的分布,牙本质缺损组比正常组中可见更多的荧光细胞,且随着牙髓炎症的恢复,荧光细胞减少。结论:牙髓损伤时,骨髓间充质干细胞可以迁移到损伤的牙髓处参与其损伤的修复。 展开更多
关键词 GFP转基因大鼠 骨髓间充质干细胞 嵌合 牙本质缺损
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Generation of rat-mouse chimeras by introducing single cells of rat inner cell masses into mouse blastocysts
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作者 TiANDa Li Leyun Wang +7 位作者 Xinxin Zhang Liyuan Jiang Yufei Li Junjie Mao Tongtong Cui Wei Li Liu Wang Qi Zhou 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2018年第6期325-328,共4页
In the field of developmental biology and regenerative medicine,mammalian interspecific chimeras have been proved very useful for investigating early embryonic development and the immune system establishment,and exten... In the field of developmental biology and regenerative medicine,mammalian interspecific chimeras have been proved very useful for investigating early embryonic development and the immune system establishment,and extended to a promising potential for human organ generation(Rossant et al.,1982). 展开更多
关键词 Generation of rat-mouse chimeras by introducing single cells of rat inner cell masses into mouse blastocysts GFP
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Derivation of embryonic stem cells from Brown Norway rats blastocysts 被引量:5
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作者 Xiaoyang Zhao Zhuo Lv +3 位作者 Lei Liu Liu Wang Man Tong Qi Zhou 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2010年第7期467-473,共7页
Knockout Brown Norway (BN) rat could be a useful disease model for human disorders,however,a failure to derive embryonic stem (ES) cells disturbs the further development of the model.In this study,we reported a ca... Knockout Brown Norway (BN) rat could be a useful disease model for human disorders,however,a failure to derive embryonic stem (ES) cells disturbs the further development of the model.In this study,we reported a case of successful derivation of the BN rat ES cells with the derivation efficiency comparable to that of Sprague Dawley (SD) rats.The BN rat ES cells expressed the key transcription factors,and were able to form embryonic bodies (EBs) when being differentiated in vitro.After injecting the BN rat ES cells into the SD rat blastocysts,high-contribution chimeric rats were generated and could survive to their adulthood.Our success in generating pluripotent rat ES cells will benefit the generation of the knockout rats in the future. 展开更多
关键词 Brown Norway (BN) rat embryonic stem cells PLURIPOTENCY chimera rat
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