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  • [Biomedicines.] Interleukin-4 Receptor Targeting Peptide Decorated Extracellular Vesicles as a Platform for In Vivo Drug Delivery to Thyroid Cancer

    2022년 10월호
    [Biomedicines.] Interleukin-4 Receptor Targeting Peptide Decorated Extracellular Vesicles as a Platform for In Vivo Drug Delivery to Thyroid Cancer

    경북대 / Prakash Gangadaran, 안병철*

  • 출처
    Biomedicines.
  • 등재일
    2022 Aug 15
  • 저널이슈번호
    10(8):1978. doi: 10.3390/biomedicines10081978.
  • 내용

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    Abstract
    Mesenchymal stem cell (MSC)-derived extracellular vesicles (EVs) have been demonstrated to deliver therapeutic drugs in preclinical studies. However, their use is limited, as they lack the ability to specifically deliver drugs to tumor tissues in vivo. In the present study, we propose the use of a targeting peptide, IL-4R-binding peptide (IL4RPep-1), to specifically deliver intravenously (i.v.) infused EVs to thyroid tumors. In vivo, a xenograft tumor model was treated with either the control peptide (NSSSVDK) or IL4RPep-1-Flamma; mice were fluorescently imaged (FLI) using an in vivo imaging system at 0-3 h post-treatment. EVs (labeled with DiD dye) were conjugated with IL4RPep-1 through a DOPE-NHS linker and administered to mice intravenously. FLI was performed 0-24 h post-injection, and the animals were sacrificed for further experiments. The morphology and size of EVs, the presence of EV markers such as CD63 and ALIX, and the absence of the markers GM130 and Cyto-C were confirmed. In vivo, FLI indicated an accumulation of i.v. injected IL4RPep-1-Flamma at the tumor site 90 min post-injection. No accumulation of NSSSVDK-Flamma was detected. In vivo, IL4RPep-1-EVs targeted the Cal-62 tumor 2 h post-injection. NSSSVDK-EVs were not even detected in the tumor 24 h post-injection. The quantification of FLI showed a significant accumulation of MSC-EVs in the tumor 2 h, 3 h, and 24 h post-injection. Furthermore, ex vivo imaging and an IF analysis confirmed the in vivo findings. Our results demonstrate the use of the IL4RPep-1 peptide as a targeting moiety of EVs for IL-4R-expressing anaplastic thyroid tumors.

     

     

    Affiliations

    Prakash Gangadaran  1   2 , Gowri Rangaswamy Gunassekaran  3 , Ramya Lakshmi Rajendran  2 , Ji Min Oh  2 , Sri Murugan Poongkavithai Vadevoo  3 , Ho Won Lee  2 , Chae Moon Hong  2   4 , Byungheon Lee  1   3 , Jaetae Lee  2   4 , Byeong-Cheol Ahn  1   2   4
    1 BK21 FOUR KNU Convergence Educational Program of Biomedical Sciences for Creative Future Talents, Department of Biomedical Sciences, School of Medicine, Kyungpook National University, Daegu 41944, Korea.
    2 Department of Nuclear Medicine, School of Medicine, Kyungpook National University, Daegu 41944, Korea.
    3 Department of Biochemistry and Cell Biology, Kyungpook National University, Daegu 41944, Korea.
    4 Department of Nuclear Medicine, Kyungpook National University Hospital, Daegu 41944, Korea.

  • 키워드
    IL-4R-binding peptide; anaplastic thyroid cancer; drug delivery; extracellular vesicles; interleukin-4 receptor.
  • 연구소개
    세포밖소포체(Extracellular vesicles; EV)는 다양한 질환에서 치료제로서의 가능성이 기대대고 있다. 또한 EV는 약제전달체로서의 가능성도 기대되고 있다. 본 연구에서는 EV에 종양 추적 기능이 있는 펩타이드를 표지하면 종양 추적능을 높이는 결과를 보여줄 수 있다는 연구이다. 이 연구에서 사용한 펩타이드는 IL-4 수용체를 추적할 수 있는 펩타이드이며, 다양향 종양에서 IL-4 수용체가 발현되는 것으로 알려져 있다. 이 연구는 종양치료에 EV를 사용한다면 EV에 종양추적 moiety를 도입하면 더 양호한 결과를 나타낼 수 있음을 보여준다.
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