In vitro construction of a recombinant human embryonic brain-derived neurotrophin-4 gene and pEGFP-N1 vector
Jintao Li
Qi Yan
Xingbao Zhu
Dan Xu
Tinghua Wang
Huatang Zhang
Jia Liu
摘要:BACKGROUND: Neurotrophin-4 (NT-4) can promote neuronal growth, development, differentiation, maturation, and survival. NT-4 can also improve recovery and regeneration of injured neurons, but cannot pass through the blood-brain barrier, which limits its activity in the central nervous system. Delivering NT-4 into the central nervous system via cells or vectors may have therapeutic benefit.OBJECTIVE: To construct a recombinant vector with a human embryonic brain-derived NT-4 gene and pEGFP-N1.DESIGN, TIME AND SETTING: Neural genetic engineering experiment. The study was performed at the Neuroscience Institute of Kunming Medical College between October 2007 and March 2008.MATERIALS: The pEGFP-N1 plasmid vector was provided by Kunming Institute of Zoology, Chinese Academy of Sciences; embryonic brain tissues were provided by the First Affiliated Hospital of Kunming Medical College. TRIzol RNA extraction Kit was purchased from Sigma (USA), One Step RNA PCR Kit (AMV) etc. were from Takara (Dalian, China).METHODS: Total RNA was extracted from human embryonic brain tissues using Trizol. The agarose gel electrophoresis showed two bands: 18 S and 28 S, which were essential subunits of total RNA. The human NT-4 DNA was obtained via RT-PCR and inserted into the pEGFP-N1 vector using ligation and transformation reaction.MAIN OUTCOME MEASURES: The sequencing results of the DNA in the recombinant of NT-4-pEGFP-N1.RESULTS: The NT-4-pEGFP-N1 vector was sequence-verified and showed the expected molecular weight.CONCLUSION: The recombinant of NT-4-pEGFP-N1 was constructed successfully in vitro.
机标关键词:central nervous systemNT-4First Affiliated Hospitalgenetic engineeringgel electrophoresisrecombinant vectorprovidedhuman
资助基金:(No. 07C10388)
论文发表日期:2009-01-01
在线出版日期:2025-08-15(本平台首次上网日期,不代表文献的发表时间)
页数:4( 312-315 )
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中国神经再生研究(英文版)

中国神经再生研究(英文版)

CSTPCDSCI
ISSN:1673-5374
年,卷(期):2009,4(4)
所属栏目:Techniques and Methods