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Minicircle microporation-based non-viral gene delivery improved the targeting of mesenchymal stem cells to an injury site

첫 페이지 보기
  • 발행기관
    한국당과학회 바로가기
  • 간행물
    한국당과학회 학술대회 바로가기
  • 통권
    2017 한국당과학회 동계학술대회 (2017.01)바로가기
  • 페이지
    pp.42-42
  • 저자
    Ji-Young Mun, Keun Koo Shin, Doo-Byoung Oh
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A294800

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원문정보

초록

영어
Genetic engineering approaches to improve therapeutic potentials of mesenchymal stem cells (MSCs) have been made by viral or non-viral gene delivery methods. Viral methods have severe limitations in clinical application due to potential oncogenic, pathogenic, and immunogenic risks while non-viral ones have suffered from low transfection efficiency and transient weak expression as MSCs are hard-to-transfect cells. In this study, minicircle, which is a minimal expression vector free of bacterial sequences, was employed for MSC transfection as a non-viral gene delivery. Conventional cationic liposome method was not effective for MSC transfection to result in very low transfection efficiency (less than 5%). Microporation, a new electroporation method, greatly improved the transfection efficiency of minicircles up to 66% in MSCs without significant loss of cell viability. Furthermore, minicircle microporation generated much stronger and prolonged transgene expression, compared to plasmid microporation. When the MSCs transfected to express firefly luciferase by minicircle microporation were subcutaneously injected to mice, their bioluminescence was monitored for more than a week whereas the bioluminescence of the MSCs induced by plasmid microporation rapidly decreased and disappeared in mice within three days. By using minicircle microporation as a non-viral gene delivery, the engineered MSCs to overexpress CXCR4 were shown to have greatly increased homing ability toward the injury site through in vivo bioluminescence imaging in mice, which showed a promise to enhance therapeutic potentials of MSCs in clinical applications.

저자

  • Ji-Young Mun [ Synthetic Biology and Bioengineering Research Center, Korean Research Institute of Bioscience & Biotechnology, Daejeon 305-806, Korea ]
  • Keun Koo Shin [ Synthetic Biology and Bioengineering Research Center, Korean Research Institute of Bioscience & Biotechnology, Daejeon 305-806, Korea ]
  • Doo-Byoung Oh [ Synthetic Biology and Bioengineering Research Center, Korean Research Institute of Bioscience & Biotechnology, Daejeon 305-806, Korea ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국당과학회 [Korean Society for Glycoscience]
  • 설립연도
    2006
  • 분야
    의약학>약학
  • 소개
    본 학회는 화학, 생화학, 분자생물학, 미생물학, 식품공학, 의학, 약학, 유전공학 및 생물공학, 환경 및 기타 공업 등 전 분야의 탄수화물관련 이론과 기술을 연구 발전시키고 산학협동을 통해 이를 보급하여 국내 관련 산업의 발전 및 국민생활의 과학화에 기여하고자 하며, 이러한 목표와 비젼의 실현을 위해 회원들이 적극적인 참여와 활동을 전개하고자 한다.

간행물

  • 간행물명
    한국당과학회 학술대회
  • 간기
    연간
  • 수록기간
    2006~2022
  • 십진분류
    KDC 517 DDC 614

이 권호 내 다른 논문 / 한국당과학회 학술대회 2017 한국당과학회 동계학술대회

    피인용수 : 0(자료제공 : 네이버학술정보)

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