敲减SOX9基因对骨髓间充质干细胞表达的影响
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作者Author单位AddressE-Mail
梁大川 LIANG Da-chuan 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China  
白洁玉 BAI Jie-yu 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China  
杜少华 DU Shao-hua 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China  
程鹏 CHENG Peng 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China  
王震 WANG Zhen 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China  
康宁 KANG Ning 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China  
杨自权 YANG Zi-quan 山西医科大学第二医院骨科 骨与软组织损伤修复山西省重点实验室, 山西 太原 030001 Department of Orthopaedics, the Second Hospital Affiliated to Shanxi Medical Univeristy, Taiyuan 030001, Shanxi, China yzqonline@126.com 
期刊信息:《中国骨伤》2013年,第26卷,第9期,第760-763页
DOI:10.3969/j.issn.1003-0034.2013.09.014
基金项目:国家自然科学基金资助项目(编号:30973048);国际科技合作项目(编号:2010DFA32450);国家人事部及山西省人事厅留学回国人员科技活动择优资助项目;山西省留学基金项目(编号 :107);山西省自然科学基金资助项目(编号:2010011050-6)
中文摘要:

目的:构建小鼠S0X9基因干扰的慢病毒载体,体外转染小鼠骨髓间充质干细胞,观察小鼠SOX9基因在小鼠间充质干细胞中的表达影响.

方法:针对小鼠SOX9基因序列,设计RNA干扰靶点序列,合成含干扰序列的双链DNAoligo连入酶切后的RNA干扰载体上,构建Lenti-SOX9-siRNA-EGFP载体,鉴定扩增.利用SOX9基因沉默载体体外转染小鼠骨髓间充质细胞,利用倒置荧光显微镜观察转染是否成功,并通过流式细胞仪测定转染效率.同时利用RT-PCR和Western Blot检测小鼠SOX9基因的表达.

结果:成功构建了Lenti-SOX9-siRNA-EGFP,SOX9基因沉默慢病毒载体,能高效转染小鼠骨髓间充质细胞.RT-PCR和Western Blot检测显示经SOX9基因转染的小鼠骨髓间充质细胞基因表达沉默.

结论:利用慢病毒结合RNA干扰技术敲减小鼠SOX9基因成功地转染小鼠骨髓间充质干细胞,且SOX9基因在小鼠骨髓间充质干细胞中发生了沉默,这为SOX9修复软骨损伤的进一步研究奠定了基础.
【关键词】SOX9  慢病毒属  转染  骨髓间充质干细胞细胞
 
Gene expression of bone mesenehymal stem cells transduced by the lentiviral vector of SOX9 gene knockdown
ABSTRACT  

Objective:To construct one lentiviral vector containing mouse SRY-related silencing group-box gene 9 (SOX9) and to transfect murine bone mesenehymal stem cells(mBMSCs) in vitro and observe the expressi on of target gene.

Methods:RNA inteference target sequence was designed in connectin with mice SOX9 genese quence.The double strands DNAoligo containing interference sequence were synthesized and cloned into len tivirus vector.The siRNA lentiviral vector with SOX9 gene silencing was constructed and identified,which was transfected into rat bone mesenehymal stem cells.The expression of target gene was detected by immuno fluorescence,RT-PCR and Western blot.

Results:Lenti-SOX9-siRNA-EGFP was recombined successfully and tra nsduced efficiently into mBMSCs.The expression of SOX9 gene silencing was confirmed by RT-PCR and Western blot.

Conclusion:Mouse SOX9 gene silencing by RNA interference and Lentiviral vector can transfected successfully into mBMSCs.Meanwhile,SOX9 gene may be silenced in SOX9 transduced mBMSCs.This will provide targ et cells for the following study about SOX9 gene respairing cartilage injury.
KEY WORDS  SOX9  Lentivirus  Transfection  Bone mesenehymal stem cells
 
引用本文,请按以下格式著录参考文献:
中文格式:梁大川,白洁玉,杜少华,程鹏,王震,康宁,杨自权.敲减SOX9基因对骨髓间充质干细胞表达的影响[J].中国骨伤,2013,26(9):760~763
英文格式:LIANG Da-chuan,BAI Jie-yu,DU Shao-hua,CHENG Peng,WANG Zhen,KANG Ning,YANG Zi-quan.Gene expression of bone mesenehymal stem cells transduced by the lentiviral vector of SOX9 gene knockdown[J].zhongguo gu shang / China J Orthop Trauma ,2013,26(9):760~763
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