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[1]黃小龍,全仁夫,胡華輝,等.HLA-B2704基因型強直性脊柱炎患者來源的人誘導多能干細胞體系的建立[J].中醫(yī)正骨,2017,29(12):11-18.
 HUANG Xiaolong,QUAN Renfu,HU Huahui,et al.Establishment of human-induced pluripotent stem cells system originated from patients with HLA-B2704 genotypic ankylosing spondylitis[J].The Journal of Traditional Chinese Orthopedics and Traumatology,2017,29(12):11-18.
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HLA-B2704基因型強直性脊柱炎患者來源的人誘導多能干細胞體系的建立()
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《中醫(yī)正骨》[ISSN:1001-6015/CN:41-1162/R]

卷:
第29卷
期數:
2017年12期
頁碼:
11-18
欄目:
基礎研究
出版日期:
2017-12-20

文章信息/Info

Title:
Establishment of human-induced pluripotent stem cells system originated from patients with HLA-B2704 genotypic ankylosing spondylitis
作者:
黃小龍1全仁夫1胡華輝1李偉1李強1邱銳2孫亞萍3楊迪生4
1.浙江省杭州市蕭山區(qū)中醫(yī)院,浙江 杭州 311201; 2.浙江中醫(yī)藥大學,浙江 杭州 310053; 3.浙江大學,浙江 杭州 310058; 4.浙江大學附屬第二醫(yī)院,浙江 杭州 310009
Author(s):
HUANG Xiaolong1QUAN Renfu1HU Huahui1LI Wei1LI Qiang1QIU Rui2SUN Yaping3YANG Disheng4
1.Xiaoshan Hospital of Chinese Medicine,Hangzhou 311201,Zhejiang,China 2.Zhejiang Chinese Medical University,Hangzhou 310053,Zhejiang,China 3.Zhejiang University,Hangzhou 310058,Zhejiang,China 4.The Second Affiliated Hospital of Zhejiang University,Hangzhou 310009,Zhejiang,China
關鍵詞:
脊柱炎強直性 HLA抗原 尿 誘導多能干細胞
Keywords:
Key words spondylitisankylosing HLA antigens urine induced pluripotent stem cells
摘要:
目的:建立人類白細胞抗原(human leukocyte antigen,HLA)-B2704基因型強直性脊柱炎(ankylosing spondylitis,AS)患者來源的人誘導多能干細胞(human-induced pluripotent stem cells,hiPSCs)體系。方法:采用逆轉錄病毒介導的感染系統(tǒng)把OCT4、SOX2、c-MYC、KLF4這4個外源轉錄因子導入HLA-B2704基因型AS患者的尿液細胞中,重編程獲得hiPSCs。通過形態(tài)觀察、堿性磷酸酶染色、免疫熒光染色、內源多能性相關基因檢測、體外擬胚體(embryoid bodies,EBs)分化檢測、EBs三胚層基因檢測以及畸胎瘤形成實驗,鑒定獲得的hiPSCs。結果:病毒感染尿液細胞后第4天至第5天細胞核質比增大,第14天左右出現克隆,第24天后形成與人胚胎干細胞(human embryonic stem cells,hESCs)相似的克隆。堿性磷酸酶染色顯示,hiPSCs和hESCs-H1一樣,均被染成紫紅色,呈陽性。免疫熒光染色顯示,hESCs階段特異性胚胎抗原4及ESCs轉錄因子OCT4、SOX2均呈陽性。hiPSCs內源多能性基因OCT4、SOX2、NANOG和REX1的表達與H1內源多能性相關基因的表達比較,差異均無統(tǒng)計學意義(1.006±0.208,1.000±0.340,t=0.038,P=0.972; 1.061±0.140,1.000±0.387,t=0.431,P=0.689; 1.386±0.354,1.000±0.032,t=1.467,P=0.303; 1.280±0.283,1.000±0.013,t=1.398,P=0.235)。EBs高表達內胚層基因AFP、GATA4,中胚層基因MEX1、TBX1,外胚層基因PAX6、SOX1; EBs三胚層基因AFP、GATA4、TBX1、MSX1、PAX6、SOX1的相對表達量均高于hiPSCs(60.695±8.746,1.000±0.245,t=9.647,P=0.011; 3.724±0.144,1.000±0.417,t=12.136,P=0.007; 4.224±0.869,1.000±0.130,t=4.988,P=0.038; 684.800±63.326,1.000±0.211,t=15.270,P=0.004; 131.561±15.785,1.000±0.232,t=11.700,P=0.007; 98.507±40.443,1.000±0.215,t=16.000,P=0.004)。hiPSC體內形成畸胎瘤,HE染色可見內、中、外3個胚層的組織細胞; 其中內胚層為小腸上皮組織細胞,中胚層為肌肉組織細胞,外胚層為神經上皮組織細胞。結論:采用逆轉錄病毒介導的感染系統(tǒng)把OCT4、SOX2、c-MYC、KLF4這4個外源轉錄因子導入HLA-B2704基因型AS患者的尿液細胞中,經過重編程,可成功建立HLA-B2704基因型AS患者來源hiPSCs體系。
Abstract:
ABSTRACT Objective:To establish the human-induced pluripotent stem cells(hiPSCs)system originated from patients with human leukocyte antigen(HLA)-B2704 genotypic ankylosing spondylitis(AS).Methods:Four exogenous transcription factors including OCT4,SOX2,c-MYC and KLF4 were introduced into the urinary cells(UCs)of patients with HLA-B2704 genotypic AS by using retrovirus-mediated infection system,and the infected UCs were reprogrammed for obtaining hiPSCs.The hiPSCs were identified through morphologic observation,alkaline phosphatase staining,immunofluorescence staining,endogenous multipotent related gene detection,embryoid bodies(EBs)differentiation detection,EBs triploblastic gene detection and teratoma formation experiment.Results:The nuclear-cytoplasmic ratioincreased at the 4th and 5th day after UCs were infected by virus.The clone appeared at the 14th day and it was similar to human embryonic stem cells(hESCs)at the 24th day.The result of alkaline phosphatase staining showed that both hiPSCs and hESCs-H1 were presented with prunosus positive staining.The result of immunofluorescent staining showed that the stage specific embryonic antigen 4(SSEA4)of hESCs and the transcription factor of ESCs including OCT4 and SOX2 presented with positive staining.There was no statistical difference in the expression of endogenous multipotent related gene including OCT4,SOX2,NANOG and REX1 between hiPSCs and hiPSCs-H1(1.006+/-0.208 vs 1.000+/-0.340,t=0.038,P=0.972; 1.061+/-0.140 vs 1.000+/-0.387,t=0.431,P=0.689; 1.386+/-0.354,1.000+/-0.032,t=1.467,P=0.303; 1.280+/-0.283 vs 1.000+/-0.013,t=1.398,P=0.235).High expressions of endodermal genes including AFP and GATA4,mesodermal genes including MEX1 and TBX1 and ectodermal genes including PAX6 and SOX1 were found in EBs.The relative expression levels of triploblastic genes including AFP,GATA4,TBX1,MSX1,PAX6 and SOX1 were higher in EBs compared to hiPSCs(60.695+/-8.746 vs 1.000+/-0.245,t=9.647,P=0.011; 3.724+/-0.144 vs 1.000+/-0.417,t=12.136,P=0.007; 4.224+/-0.869 vs 1.000+/-0.130,t=4.988,P=0.038; 684.800+/-63.326 vs 1.000+/-0.211,t=15.270,P=0.004; 131.561+/-15.785 vs 1.000+/-0.232,t=11.700,P=0.007; 98.507+/-40.443 vs 1.000+/-0.215,t=16.000,P=0.004).Teratoma appeared in hiPSC.Small intestine epithelial histocytes,muscular histocytes and neuroepithelial histocytes were found respectively in entoderm,mesoderm and ectoderm of teratoma through HE staining.Conclusion:The hiPSCs system originated from patients with HLA-B2704 genotypic AS can be successfully established through introducing four exogenous transcription factors including OCT4,SOX2,c-MYC and KLF4 into UCs of patients with HLA-B2704 genotypic AS by using retrovirus-mediated infection system and reprogramming the UCs.

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備注/Memo

備注/Memo:
基金項目:浙江省科技計劃項目(2014C03031) 通訊作者:全仁夫 E-mail:[email protected]
更新日期/Last Update: 2018-05-02