体内
腺相关病毒
微球
化学
转染
基因转移
基因传递
遗传增强
生物物理学
基因
生物化学
生物
化学工程
载体(分子生物学)
工程类
重组DNA
生物技术
作者
Yuta Kurashina,Sho Kurihara,Takeshi Kubota,Shuhei Takatsuka,Motoki Hirabayashi,Hajime Shimmura,Hideo Miyahara,Aiki Hioki,Yutaka Matsushita,Jumpei Muramatsu,Yuki Ogawa,Masato Fujioka,Hirotaka James Okano,Hiroaki Onoe
标识
DOI:10.1002/adhm.202303546
摘要
Abstract This 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 CaCl 2 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.
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