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Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis.

Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis. Research Abstract Details 

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  • Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis. Abstract Text:

    bo leiBo Lei,gregory e tullisGregory E Tullis,mark d kirkMark D Kirk,keqing zhangKeqing Zhang,martin l katzMartin L Katz,

    Mutations in the human protein palmitoyl thioesterase-1 (PPT-1) gene result in an autosomal recessive neurodegenerative disorder designated neuronal ceroid lipofuscinosis (NCL), type CLN1, or infantile NCL. Among the symptoms of the CLN1 disease are accumulation of autofluorescent lysosomal storage bodies in neurons and other cell types, seizures, motor and cognitive decline, blindness, and premature death. Development of an effective therapy for this disorder will be greatly assisted by the availability of suitable animal models. A mouse PPT-1 gene knockout model has recently been generated. Studies were performed to determine whether the mouse model exhibits ocular features of the human CLN1 disorder. A progressive accumulation of autofluorescent storage material in all layers of the retina was observed in the PPT-1 knockout mice. Accompanying the storage body accumulation was a modest loss of cells with nuclei in the outer and inner nuclear layers. As indicated by electroretinogram (ERG) responses, retinal function was only mildly impaired at 4 months of age but was severely impaired by 8 months, despite only modest changes in retinal morphology. The pupillary light reflex (PLR), on the other hand, was exaggerated in the knockout mice. The apparent anomaly between the ERG and the PLR findings suggests that disease-related PLR changes may be due to changes in extraocular signal processing. The pronounced ocular phenotype in the PPT-1 knockout mice makes these animals a good model for testing therapeutic interventions for treatment of the human CLN1 disorder.

    Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis. Publishing Authors By Initials

    b leiB Lei,ge tullisGE Tullis,md kirkMD Kirk,k zhangK Zhang,ml katzML Katz,

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    Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of neuroscience research

    VOLUME: 84

    Page Numbers: 1139-49

    Journal Abbreviation:

    ISSN: 0360-4012

    DAY: 3

    MONTH: Oct

    YEAR: 2006

    Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis. Information

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    LANGUAGE: eng

    NlmUniqueID: 7600111

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    Grant and Affiliation Information for Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis.

    AFFILIATION: Mason Eye Institute, University of Missouri, Columbia, Missouri 65212, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: J Neurosci Res

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