Lipid Nanoparticles Deliver mRNA to the Brain after an Intracerebral Injection

海马体 小胶质细胞 信使核糖核酸 纹状体 医学 神经科学 病毒载体 转染 载体(分子生物学) 药理学 生物 细胞生物学 免疫学 细胞培养 炎症 重组DNA 遗传学 生物化学 基因 多巴胺
作者
Jan Tůma,Y Chen,Michael G. Collins,Abhik Paul,Jie Li,Hesong Han,Rohit Sharma,Niren Murthy,Hye Young Lee
出处
期刊:Biochemistry [American Chemical Society]
卷期号:62 (24): 3533-3547 被引量:51
标识
DOI:10.1021/acs.biochem.3c00371
摘要

Neurological disorders are often debilitating conditions with no cure. The majority of current therapies are palliative rather than disease-modifying; therefore, new strategies for treating neurological disorders are greatly needed. mRNA-based therapeutics have great potential for treating such neurological disorders; however, challenges with delivery have limited their clinical potential. Lipid nanoparticles (LNPs) are a promising delivery vector for the brain, given their safer toxicity profile and higher efficacy. Despite this, very little is known about LNP-mediated delivery of mRNA into the brain. Here, we employ MC3-based LNPs and successfully deliver Cre mRNA and Cas9 mRNA/Ai9 sgRNA to the adult Ai9 mouse brain; greater than half of the entire striatum and hippocampus was found to be penetrated along the rostro-caudal axis by direct intracerebral injections of MC3 LNP mRNAs. MC3 LNP Cre mRNA successfully transfected cells in the striatum (∼52% efficiency) and hippocampus (∼49% efficiency). In addition, we demonstrate that MC3 LNP Cas9 mRNA/Ai9 sgRNA edited cells in the striatum (∼7% efficiency) and hippocampus (∼3% efficiency). Further analysis demonstrates that MC3 LNPs mediate mRNA delivery to multiple cell types including neurons, astrocytes, and microglia in the brain. Overall, LNP-based mRNA delivery is effective in brain tissue and shows great promise for treating complex neurological disorders.
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