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Research Article Free access | 10.1172/JCI117434

Behavioral consequences of bone marrow transplantation in the treatment of murine mucopolysaccharidosis type VII.

L Bastedo, M S Sands, D T Lambert, M A Pisa, E Birkenmeier, and P L Chang

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Find articles by Bastedo, L. in: PubMed | Google Scholar

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Find articles by Sands, M. in: PubMed | Google Scholar

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Find articles by Lambert, D. in: PubMed | Google Scholar

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Find articles by Pisa, M. in: PubMed | Google Scholar

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Find articles by Birkenmeier, E. in: PubMed | Google Scholar

Department of Biology, McMaster University, Hamilton, Ontario, Canada.

Find articles by Chang, P. in: PubMed | Google Scholar

Published September 1, 1994 - More info

Published in Volume 94, Issue 3 on September 1, 1994
J Clin Invest. 1994;94(3):1180–1186. https://doi.org/10.1172/JCI117434.
© 1994 The American Society for Clinical Investigation
Published September 1, 1994 - Version history
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Abstract

The gusmps/gusmps mouse is a model of the human lysosomal storage disease mucopolysaccharidosis type VII caused by deficient beta-glucuronidase activity. Bone marrow transplantation has been shown to correct some of their biochemical and pathological abnormalities but its efficacy in correcting their neurological functional deficits is unknown. We transplanted the neonatal gusmps/gusmps mice and their normal controls and evaluated their central nervous system function with two behavioral tests: the grooming test, a developmentally regulated and genetically based activity, and a Morris water maze test which assessed spatial learning abilities. The two transplanted groups groomed less than the normals, were unable to remember the location of an invisible platform from day to day, and were severely impaired at developing strategies to locate the platform in unfamiliar locations. The performance of both normal and mutant transplanted groups was clearly inferior to the untreated normals and, in some instances, close to or worse than the untreated mutants, even though the enzyme abnormalities of the mutants have been partially corrected. Hence, the behavioral deficits in the mutant mice were not restored to normal while similarly treated normal mice showed significant functional deterioration, indicating the detrimental consequence of this therapy in the neonatal period.

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