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Extensive beta-glucuronidase activity in murine central nervous system after adenovirus-mediated gene transfer to

A Ghodsi1, C Stein, T Derksen

  • 1Department of Neurosurgery, University of Iowa College of Medicine, Iowa City 52242, USA.

Human Gene Therapy
|November 26, 1998
PubMed

Insights

Gene therapy using adenovirus delivered beta-glucuronidase to the mouse central nervous system. This enzyme treatment reduced cellular vacuoles in Mucopolysaccharidosis type VII mice, showing potential for lysosomal storage disorder treatment.

Area of Science:

  • Neuroscience
  • Genetics
  • Biochemistry

Background:

  • Mucopolysaccharidosis type VII (MPS VII) is a lysosomal storage disease characterized by central nervous system (CNS) pathology due to beta-glucuronidase deficiency.
  • Effective CNS enzyme delivery and cellular uptake are crucial for MPS VII therapeutic strategies.

Purpose of the Study:

  • To evaluate the efficacy of direct gene transfer using recombinant adenovirus encoding beta-glucuronidase (Ad betagluc) for treating MPS VII in the CNS.
  • To assess the distribution and persistence of beta-glucuronidase activity following Ad betagluc administration in mouse models.

Main Methods:

  • Intrastriatal, intraventricular, and cisterna magna injections of Ad betagluc were performed in MPS VII and wild-type mice.
  • Histochemical staining was used to detect beta-glucuronidase activity and distribution.
  • Histological analysis assessed the reduction of distended vacuoles in neurons and glia.

Main Results:

  • Ad betagluc resulted in widespread beta-glucuronidase mRNA and enzyme activity throughout the mouse CNS, extending beyond the injection site.
  • Sustained enzyme expression was observed for at least 84 days post-injection.
  • Beta-glucuronidase-deficient mice showed a significant reduction in neuronal and glial vacuoles in both hemispheres after treatment.

Conclusions:

  • Direct gene transfer with Ad betagluc effectively distributes functional beta-glucuronidase throughout the CNS.
  • This approach demonstrates significant therapeutic potential for treating lysosomal storage disorders like MPS VII.

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