CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model

Nat Commun. 2022 Apr 14;13(1):1847. doi: 10.1038/s41467-022-29473-4.

Abstract

Ribitol-phosphate modification is crucial for the functional maturation of α-dystroglycan. Its dysfunction is associated with muscular dystrophy, cardiomyopathy, and central nervous system abnormalities; however, no effective treatments are currently available for diseases caused by ribitol-phosphate defects. In this study, we demonstrate that prodrug treatments can ameliorate muscular dystrophy caused by defects in isoprenoid synthase domain containing (ISPD), which encodes an enzyme that synthesizes CDP-ribitol, a donor substrate for ribitol-phosphate modification. We generated skeletal muscle-selective Ispd conditional knockout mice, leading to a pathogenic reduction in CDP-ribitol levels, abnormal glycosylation of α-dystroglycan, and severe muscular dystrophy. Adeno-associated virus-mediated gene replacement experiments suggested that the recovery of CDP-ribitol levels rescues the ISPD-deficient pathology. As a prodrug treatment strategy, we developed a series of membrane-permeable CDP-ribitol derivatives, among which tetraacetylated CDP-ribitol ameliorated the dystrophic pathology. In addition, the prodrug successfully rescued abnormal α-dystroglycan glycosylation in patient fibroblasts. Consequently, our findings provide proof-of-concept for supplementation therapy with CDP-ribitol and could accelerate the development of therapeutic agents for muscular dystrophy and other diseases caused by glycosylation defects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Dystroglycans
  • Humans
  • Mice
  • Muscle, Skeletal
  • Muscular Dystrophies* / drug therapy
  • Muscular Dystrophies* / genetics
  • Phosphates
  • Prodrugs* / pharmacology
  • Prodrugs* / therapeutic use
  • Ribitol / therapeutic use

Substances

  • Dystroglycans
  • Phosphates
  • Prodrugs
  • Ribitol