In vivo neuronal gene editing via CRISPR-Cas9 amphiphilic nanocomplexes alleviates deficits in mouse models of Alzheimer's disease

  • Park, Hanseul; 
  • Oh, Jungju; 
  • Shim, Gayong; 
  • Cho, Byounggook; 
  • Chang, Yujung; 
  • ... Lee, Minhyung; 
  • 외 11명
Citations

WEB OF SCIENCE

224
Citations

SCOPUS

266

초록

In vivo gene editing in post-mitotic neurons of the adult brain may be a useful strategy for treating neurological diseases. Here, we develop CRISPR-Cas9 nanocomplexes and show they were effective in the adult mouse brain, with minimal off-target effects. Using this system to target Bacel suppressed amyloid beta (A beta)-associated pathologies and cognitive deficits in two mouse models of Alzheimer's disease. These results broaden the potential application of CRISPR-Cas9 systems to neurodegenerative diseases.

키워드

MICE; EXPRESSION; PROTEIN; MUSCLE
제목
In vivo neuronal gene editing via CRISPR-Cas9 amphiphilic nanocomplexes alleviates deficits in mouse models of Alzheimer's disease
저자
Park, Hanseul; Oh, Jungju; Shim, Gayong; Cho, Byounggook; Chang, Yujung; Kim, Siyoung; Baek, Soonbong; Kim, Hongwon; Shin, Jeain; Choi, Hwan; Yoo, Junsang; Kim, Junyeop; Jun, Won; Lee, Minhyung; Lengner, Christopher J.; Oh, Yu-Kyoung; Kim, Jongpil
DOI
10.1038/s41593-019-0352-0
발행일
2019-04
유형
Article
저널명
Nature Neuroscience
권
22
호
4
페이지
524 ~ 528