Adeno‐Associated Virus‐Encapsulated Alginate Microspheres Loaded in Collagen Gel Carriers for Localized Gene Transfer

Author:

Kurashina Yuta12ORCID,Kurihara Sho34,Kubota Takeshi5,Takatsuka Shuhei5,Hirabayashi Motoki34,Shimmura Hajime34,Miyahara Hideo5,Hioki Aiki5,Matsushita Yutaka34,Muramatsu Jumpei5,Ogawa Yuki4,Fujioka Masato678,Okano Hirotaka J.4,Onoe Hiroaki1ORCID

Affiliation:

1. Department of Mechanical Engineering Faculty of Science and Technology Keio University 3‐14‐1 Hiyoshi Kohoku‐ku Yokohama 223–8522 Japan

2. Division of Advanced Mechanical Systems Engineering Institute of Engineering Tokyo University of Agriculture and Technology 2‐24‐16 Nakacho Koganei‐shi Tokyo 184–8588 Japan

3. Department of Otorhinolaryngology The Jikei University School of Medicine 3‐25‐8 Nishishimbashi Minato‐ku Tokyo 105–8461 Japan

4. Division of Regenerative Medicine The Jikei University School of Medicine 3‐25‐8 Nishishimbashi Minato‐ku Tokyo 105–8461 Japan

5. School of Integrated Design Engineering Graduate School of Science and Technology Keio University 3‐14‐1 Hiyoshi Kohoku‐ku Yokohama 223–8522 Japan

6. Department of Molecular Genetics Kitasato University School of Medicine 1‐15‐1 Kitasato, Minami‐ku Sagamihara Kanagawa 252–0374 Japan

7. Clinical and Translational Research Center Keio University Hospital 35 Shinanomachi Shinjuku‐ku Tokyo 160–8582 Japan

8. Department of Otorhinolaryngology Head and Neck Surgery Keio University School of Medicine 35 Shinanomachi, Shinjuku‐ku Tokyo 160–8582 Japan

Abstract

AbstractThis work reports localized in vivo gene transfer by biodegradation of the adeno‐associated virus‐encapsulating alginate microspheres (AAV‐AMs) loaded in collagen gel carriers. AAV‐AMs are centrifugally synthesized by ejecting a mixed pre‐gel solution of alginate and AAV to CaCl2 solution to form an ionically cross‐linked hydrogel microsphere immediately. The AAV‐AMs are able to preserve the AAV without diffusing out even after spreading them on the cells, and the AAV is released and transfected by the degradation of the alginate microsphere. In addition, AAV‐AMs can be stored by cryopreservation until use. By implanting this highly convenient AAV‐encapsulated hydrogel, AAV‐AMs can be loaded into collagen gel carriers to fix the position of the implanted AAV‐AMs and achieve localized gene transfer in vivo. In vivo experiments show that the AAV‐AMs loaded in collagen gel carriers are demonstrated to release the encapsulated AAV for gene transfer in the buttocks muscles of mice. While conventional injections caused gene transfer to the entire surrounding tissue, the biodegradation of AAV‐AMs shows that gene transfer is achieved locally to the muscles. This means that the proposed AAV‐loaded system is shown to be a superior method for selective gene transfer.

Funder

Japan Agency for Medical Research and Development

Publisher

Wiley

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