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Abstract
CRISPR/Cas9-mediated gene activation is a potential therapeutic strategy that does not induce double-strand break (DSB) DNA damage. However, in vivo gene activation via a Cas9 activator remains a challenge, currently limiting its therapeutic applications. We developed a Cas9 activator nanocomplex that efficiently activates an endogenous gene in the brain in vivo, suggesting its possible application in novel therapeutics. We demonstrated a potential treatment application of the Cas9 activator nanocomplex by activating Adam10 in the mouse brain without introducing insertions and deletions (inDels). Remarkably, in vivo activation of Adam10 with the Cas9 activator nanocomplex improved cognitive deficits in an Alzheimer's disease (AD) mouse model. These results demonstrate the therapeutic potential of Cas9 activator nanocomplexes for a wide range of neurological diseases.

Affiliations

Hanseul Park  1 , Yerim Hwang  1 , Jongpil Kim  2
1 Laboratory of Cell Reprogramming & Gene Editing, Department of Chemistry & Biomedical Engineering, Dongguk University, Seoul, 04620, Republic of Korea.
2 Laboratory of Cell Reprogramming & Gene Editing, Department of Chemistry & Biomedical Engineering, Dongguk University, Seoul, 04620, Republic of Korea. Electronic address: jk2316@gmail.com.