Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy

Lina S. Correa-Cerro, Christopher A. Wassif, Lisa Kratz, Georgina F. Miller, Jeeva P. Munasinghe, Alexander Grinberg, Steven J. Fliesler, Forbes D. Porter

Research output: Contribution to journalArticlepeer-review

Abstract

Smith-Lemli-Opitz syndrome (SLOS) is a genetic syndrome caused by mutations in the 3β-hydroxysterol Δ7-reductase gene (DHCR7). SLOS patients have decreased cholesterol and increased 7-dehydrocholesterol (7-DHC) levels. Dietary cholesterol supplementation improves systemic biochemical abnormalities; however, because of the blood-brain barrier, the central nervous system (CNS) is not treated. Simvastatin therapy has been proposed as a means to treat the CNS. Mice homozygous for a null disruption of Dhcr7, Dhcr7Δ3-5/Δ3-5, die soon after birth, thus they cannot be used to study postnatal development or therapy. To circumvent this problem, we produced a hypomorphic SLOS mouse model by introducing a mutation corresponding to DHCR7T93M. Both Dhcr7T93M/T93M and Dhcr7Δ3-5/T93M mice are viable. Phenotypic findings in Dhcr7T93M/Δ3-5 mice include CNS ventricular dilatation and two to three syndactyly. Biochemically, both Dhcr7T93M/T93M and Dhcr7T93M/Δ3-5 mice have elevated tissue 7-DHC levels; however, the biochemical defect improved with age. This has not been observed in human patients, and is due to elevated Dhcr7 expression in mouse tissues. Dietary cholesterol therapy improved sterol profiles in peripheral, but not CNS tissues. However, treatment of Dhcr7T93M/Δ3-5 mice with simvastatin decreased 7-DHC levels in both peripheral and brain tissues. Expression of Dhcr7 increased in Dhcr7T93M/Δ3-5 tissues after simvastatin therapy, consistent with the hypothesis that simvastatin therapy improves the biochemical phenotype by increasing the expression of a Dhcr7 allele with residual enzymatic activity. We conclude that simvastatin treatment is efficacious in improving the SLOS-associated sterol abnormality found in the brain, and thus has the potential to be an effective therapeutic intervention for behavioral and learning problems associated with SLOS.

Original languageEnglish (US)
Pages (from-to)839-851
Number of pages13
JournalHuman molecular genetics
Volume15
Issue number6
DOIs
StatePublished - Mar 2006

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

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