Blood-brain barrier-penetrating single CRISPR-Cas9 nanocapsules for effective and safe glioblastoma gene therapy.
Bingyang ShiXinhong SunQingshan YangBingyang ShiOlga ShimoniWeimin RuanFeiyan ZhuDongya ZhangJinlong YinXiangang HuangWei TaoJong Bae ParkXing-Jie LiangKam W LeongBingyang ShiPublished in: Science advances (2022)
We designed a unique nanocapsule for efficient single CRISPR-Cas9 capsuling, noninvasive brain delivery and tumor cell targeting, demonstrating an effective and safe strategy for glioblastoma gene therapy. Our CRISPR-Cas9 nanocapsules can be simply fabricated by encapsulating the single Cas9/sgRNA complex within a glutathione-sensitive polymer shell incorporating a dual-action ligand that facilitates BBB penetration, tumor cell targeting, and Cas9/sgRNA selective release. Our encapsulating nanocapsules evidenced promising glioblastoma tissue targeting that led to high PLK1 gene editing efficiency in a brain tumor (up to 38.1%) with negligible (less than 0.5%) off-target gene editing in high-risk tissues. Treatment with nanocapsules extended median survival time (68 days versus 24 days in nonfunctional sgRNA-treated mice). Our new CRISPR-Cas9 delivery system thus addresses various delivery challenges to demonstrate safe and tumor-specific delivery of gene editing Cas9 ribonucleoprotein for improved glioblastoma treatment that may potentially be therapeutically useful in other brain diseases.
Keyphrases
- crispr cas
- genome editing
- gene therapy
- blood brain barrier
- cerebral ischemia
- cancer therapy
- single cell
- cell therapy
- white matter
- resting state
- gene expression
- stem cells
- multiple sclerosis
- type diabetes
- insulin resistance
- drug delivery
- functional connectivity
- bone marrow
- smoking cessation
- high fat diet induced
- neuroendocrine tumors