中华医学杂志
中華醫學雜誌
중화의학잡지
National Medical Journal of China
2014年
27期
2143-2147
,共5页
刘新秀%陈嘉瑜%李小刚%高绍荣%邓敏
劉新秀%陳嘉瑜%李小剛%高紹榮%鄧敏
류신수%진가유%리소강%고소영%산민
肌萎缩侧索硬化%诱导多功能干细胞%运动神经元%超氧化物歧化酶
肌萎縮側索硬化%誘導多功能榦細胞%運動神經元%超氧化物歧化酶
기위축측색경화%유도다공능간세포%운동신경원%초양화물기화매
Amyotrophic lateral sclerosis%Induced pluripotent stem cell%Motor neuron%SOD1
目的 建立家族性肌萎缩侧索硬化(ALS)患者特异性的诱导性多能干细胞(iPS细胞)系,并诱导其分化为运动神经元,为研究中国人群ALS发病机制及药物筛选提供疾病模型.方法 通过逆转录病毒导入外源性的yamanaka转录因子,将SOD1-V14M基因突变的ALS患者成纤维细胞诱导为iPS细胞,并采用核型分析、免疫荧光染色、定量反转录PCR、畸胎瘤形成等实验对iPS细胞进行全能性鉴定,通过抑制SMAD信号通路诱导iPS细胞分化为运动神经元.结果 建立了SOD1-V14M基因突变的ALS病人特异性的iPS细胞系,验证具有全能性,并成功分化为运动神经元.结论 SOD1基因突变不影响成纤维细胞的重编程及iPS细胞的多能性,也不阻碍iPS细胞定向分化为运动神经元.本研究成功建立了SOD1-V14M基因突变的ALS患者iPS细胞系,为中国汉族人群家族性ALS疾病的研究及药物筛选提供了不可替代的资源.
目的 建立傢族性肌萎縮側索硬化(ALS)患者特異性的誘導性多能榦細胞(iPS細胞)繫,併誘導其分化為運動神經元,為研究中國人群ALS髮病機製及藥物篩選提供疾病模型.方法 通過逆轉錄病毒導入外源性的yamanaka轉錄因子,將SOD1-V14M基因突變的ALS患者成纖維細胞誘導為iPS細胞,併採用覈型分析、免疫熒光染色、定量反轉錄PCR、畸胎瘤形成等實驗對iPS細胞進行全能性鑒定,通過抑製SMAD信號通路誘導iPS細胞分化為運動神經元.結果 建立瞭SOD1-V14M基因突變的ALS病人特異性的iPS細胞繫,驗證具有全能性,併成功分化為運動神經元.結論 SOD1基因突變不影響成纖維細胞的重編程及iPS細胞的多能性,也不阻礙iPS細胞定嚮分化為運動神經元.本研究成功建立瞭SOD1-V14M基因突變的ALS患者iPS細胞繫,為中國漢族人群傢族性ALS疾病的研究及藥物篩選提供瞭不可替代的資源.
목적 건립가족성기위축측색경화(ALS)환자특이성적유도성다능간세포(iPS세포)계,병유도기분화위운동신경원,위연구중국인군ALS발병궤제급약물사선제공질병모형.방법 통과역전록병독도입외원성적yamanaka전록인자,장SOD1-V14M기인돌변적ALS환자성섬유세포유도위iPS세포,병채용핵형분석、면역형광염색、정량반전록PCR、기태류형성등실험대iPS세포진행전능성감정,통과억제SMAD신호통로유도iPS세포분화위운동신경원.결과 건립료SOD1-V14M기인돌변적ALS병인특이성적iPS세포계,험증구유전능성,병성공분화위운동신경원.결론 SOD1기인돌변불영향성섬유세포적중편정급iPS세포적다능성,야불조애iPS세포정향분화위운동신경원.본연구성공건립료SOD1-V14M기인돌변적ALS환자iPS세포계,위중국한족인군가족성ALS질병적연구급약물사선제공료불가체대적자원.
Objective To generate familial ALS patient specific induced pluripotent stem (iPS) cell lines and motor neurons and provide a cell-based disease model for amyotrophic lateral sclerosis (ALS) in Han Chinese.Methods iPS cells were derived from familial ALS patient by introducing 4 transcription factors OCT3/4,SOX2,KLF4 and c-MYC into fibroblast cells by retroviruses.Karyotypic analysis,immunofluorescence staining and quantitative reverse transcription-polymerase chain reaction (RT-PCR) were used to identify the pluripotency of these iPS cell lines.In addition,motor neurons were derived from these iPS cells by inhibiting SMAD pathway.Results IPS cell lines were established from ALS patient carrying SOD1-V14M mutation.They had pluripotency and were similar to human ES cells.Furthermore,motor neurons were successfully induced from these iPS cells.Conclusion SOD1-V14M mutation does not affect the reprogramming of fibroblast cells and pluripotency of iPS cells,nor does it prevent differentiation of motor neurons.Furthermore,the above cell-based disease model can recapitulate key aspects of ALS pathogenesis so that it provides an indispensible resource for further elucidating ALS disease pathogenesis and screening appropriate drug candidates in Han Chinese.