首页 | 本学科首页   官方微博 | 高级检索  
检索        


Controlled release of cell-permeable gene complex from poly(L-lactide) scaffold for enhanced stem cell tissue engineering
Authors:Mi-Ra JungIn-Kyong Shim  Eun-Sung KimYoon-Jeong Park  Young-Il YangSang-Kyou Lee  Seung-Jin Lee
Institution:
  • a Department of Pharmacy, Ewha Womans University, Daehyun-dong, Seodaemun-gu, Seoul 120-750, Republic of Korea
  • b Department of Biotechnology, College of Engineering, Yonsei University, Sinchon-dong, Seodaemun-gu, Seoul 120-749, Republic of Korea
  • c Department of Craniomaxillofacial Reconstructive Science, School of Dentistry, Seoul National University, Yongon-dong, Chongno-gu, Seoul 110-749, Republic of Korea
  • d Department of Pathology, College of Medicine, Inje University, Gaegeum-dong, Jin-gu, Busan 614-735, Republic of Korea
  • Abstract:The use of tissue engineering to deliver genes to stem cells has been impeded by low transfection efficiency of the inserted gene and poor retention at the target site. Herein, we describe the use of non-viral gene transfer by cell-permeable peptide (CPP) to increase the transfection efficiency. The combination of this technique with the use of a controlled release concept using a poly (l-lactide) scaffold allowed for prolonged uptake in stem cells. High transfection efficiency was obtained using a human-derived arginine-rich peptide denoted as Hph-1 (YARVRRRGPRR). The formation of complex between pDNA and Hph-1 was monitored using gel retardation tests to measure size and zeta potential. Complex formation was further assessed using a DNase I protection assay. A sustained gene delivery system was developed using a fibrous 3-D scaffold coated with pDNA/Hph-1 complexes. Transfection efficiency and the mean fluorescence intensity of human adipose-derived stem cells (hASCs) on the sustained delivery scaffold were compared to those of cells transfected via bolus delivery. Plasmid DNA completely bound Hph-1 at a negative-to-positive (N/P) charge ratio of 10. After complex formation, Hph-1 appeared to effectively protect pDNA against DNase I attack and exhibited cytotoxicity markedly lower than that of the pDNA/PEI complex. Plasmid DNA/Hph-1 complexes were released from the scaffolds over 14 days and were successfully transfected hASCs seeded on the scaffolds. Flow cytometry revealed that the transfection efficiency in hASCs treated with pDNA/Hph-1 complex was approximately 5-fold higher than that in cells transfected using Lipofectamine. The sustained delivery system showed a significantly higher transfection efficiency and remained able to transfect cells for a longer period of time than bolus delivery. These results suggest that cell-scaffold-based tissue regeneration can be further improved by transduction concept using CPP and controlled release using polymeric scaffold.
    Keywords:Tissue engineering  Gene delivery  Gene transfection of stem cells  Human adipose-derived stem cells  Cell-permeable peptide  PLLA fibrous 3-D scaffold
    本文献已被 ScienceDirect 等数据库收录!
    设为首页 | 免责声明 | 关于勤云 | 加入收藏

    Copyright©北京勤云科技发展有限公司  京ICP备09084417号