Selective suppression of polyglutamine-expanded protein by lipid nanoparticle-delivered siRNA targeting CAG expansions in the mouse CNS

Tomoki Hirunagi, Kentaro Sahashi, Kiyoshi Tachikawa, Angel I. Leu, Michelle Nguyen, Rajesh Mukthavaram, Priya P. Karmali, Padmanabh Chivukula, Genki Tohnai, Madoka Iida, Kazunari Onodera, Manabu Ohyama, Yohei Okada, Hideyuki Okano, Masahisa Katsuno

Research output: Contribution to journalArticlepeer-review

Abstract

Polyglutamine (polyQ) diseases are inherited neurodegenerative disorders caused by expansion of cytosine-adenine-guanine (CAG)-trinucleotide repeats in causative genes. These diseases include spinal and bulbar muscular atrophy (SBMA), Huntington's disease, dentatorubral-pallidoluysian atrophy, and spinocerebellar ataxias. Targeting expanded CAG repeats is a common therapeutic approach to polyQ diseases, but concomitant silencing of genes with normal CAG repeats may lead to toxicity. Previous studies have shown that CAG repeat-targeting small interfering RNA duplexes (CAG-siRNAs) have the potential to selectively suppress mutant proteins in in vitro cell models of polyQ diseases. However, in vivo application of these siRNAs has not yet been investigated. In this study, we demonstrate that an unlocked nucleic acid (UNA)-modified CAG-siRNA shows high selectivity for polyQ-expanded androgen receptor (AR) inhibition in in vitro cell models and that lipid nanoparticle (LNP)-mediated delivery of the CAG-siRNA selectively suppresses mutant AR in the central nervous system of an SBMA mouse model. In addition, a subcutaneous injection of the LNP-delivered CAG-siRNA efficiently suppresses mutant AR in the skeletal muscle of the SBMA mouse model. These results support the therapeutic potential of LNP-delivered UNA-modified CAG-siRNAs for selective suppression of mutant proteins in SBMA and other polyQ diseases. Mutant-allele selective suppression by CAG repeat-targeting oligonucleotides is a promising therapeutic approach to polyglutamine diseases. Hirunagi et al. demonstrate selective suppression of polyglutamine-expanded androgen receptor by lipid nanoparticle-mediated delivery of siRNA targeting CAG expansions in the mouse CNS of an SBMA mouse model.

Original languageEnglish
Pages (from-to)1-10
Number of pages10
JournalMolecular Therapy - Nucleic Acids
Volume24
DOIs
Publication statusPublished - 2021 Jun 4

Keywords

  • CAG repeat
  • SBMA
  • androgen receptor
  • lipid nanoparticle
  • polyglutamine diseases
  • selective suppression
  • siRNA
  • unlocked nucleic acid

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

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