Chronic enzyme replacement therapy ameliorates neuropathology in alpha-mannosidosis mice

Markus Damme, Stijn Stroobants, Meike Lüdemann, Michelle Rothaug, Renate Lüllmann-Rauch, Hans Christian Beck, Annika Ericsson, Claes Andersson, Jens Fogh, Rudi D'Hooge, Paul Saftig, Judith Blanz*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Objective: The lysosomal storage disease alpha-mannosidosis is caused by the deficiency of the lysosomal acid hydrolase alpha-mannosidase (LAMAN) leading to lysosomal accumulation of neutral mannose-linked oligosaccharides throughout the body, including the brain. Clinical findings in alpha-mannosidosis include skeletal malformations, intellectual disabilities and hearing impairment. To date, no curative treatment is available. We previously developed a beneficial enzyme replacement therapy (ERT) regimen for alpha-mannosidase knockout mice, a valid mouse model for the human disease. However, humoral immune responses against the injected recombinant human alpha-mannosidase (rhLAMAN) precluded long-term studies and chronic treatment. Methods: Here, we describe the generation of an immune-tolerant alpha-mannosidosis mouse model that allowed chronic injection of rhLAMAN by transgenic expression of a catalytically inactive variant of human LAMAN in the knockout background. Results: Chronic ERT of rhLAMAN revealed pronounced effects on primary substrate storage throughout the brain, normalization of lysosomal enzyme activities and morphology as well as a decrease in microglia activation. The positive effect of long-term ERT on neuronal lysosomal function was reflected by an improvement of cognitive deficits and exploratory activity. in vivo and in vitro uptake measurements indicate rapid clearance of rhLAMAN from circulation and a broad uptake into different cell types of the nervous system. Interpretation: Our data contribute to the understanding of neurological disorders treatment by demonstrating that lysosomal enzymes such as rhLAMAN can penetrate into the brain and is able to ameliorate neuropathology.

Original languageEnglish (US)
Pages (from-to)987-1001
Number of pages15
JournalAnnals of clinical and translational neurology
Volume2
Issue number11
DOIs
StatePublished - Nov 2015

ASJC Scopus subject areas

  • Neuroscience(all)
  • Clinical Neurology

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