دورية أكاديمية

Aspartoacylase-LacZ Knockin Mice: An Engineered Model of Canavan Disease.

التفاصيل البيبلوغرافية
العنوان: Aspartoacylase-LacZ Knockin Mice: An Engineered Model of Canavan Disease.
المؤلفون: Mersmann, Nadine, Tkachev, Dmitri, Jelinek, Ruth, Röth, Philipp Thomas, Möbius, Wiebke, Ruhwedel, Torben, Rühle, Sabine, Weber-Fahr, Wolfgang, Sartorius, Alexander, Klugmann, Matthias
المصدر: PLoS ONE; 2011, Vol. 6 Issue 5, p1-14, 14p
مصطلحات موضوعية: ASPARTOACYLASE, CANAVAN disease, GENETIC mutation, ASPARTATES, GALACTOSIDASES, SCHWANN cells
مستخلص: Canavan Disease (CD) is a recessive leukodystrophy caused by loss of function mutations in the gene encoding aspartoacylase (ASPA), an oligodendrocyte-enriched enzyme that hydrolyses N-acetylaspartate (NAA) to acetate and aspartate. The neurological phenotypes of different rodent models of CD vary considerably. Here we report on a novel targeted aspa mouse mutant expressing the bacterial b-Galactosidase (lacZ) gene under the control of the aspa regulatory elements. X-Gal staining in known ASPA expression domains confirms the integrity of the modified locus in heterozygous aspa lacZ-knockin (aspalacZ/+) mice. In addition, abundant ASPA expression was detected in Schwann cells. Homozygous (aspalacZ/lacZ) mutants are ASPA-deficient, show CD-like histopathology and moderate neurological impairment with behavioural deficits that are more pronounced in aspalacZ/lacZ males than females. Non-invasive ultrahigh field proton magnetic resonance spectroscopy revealed increased levels of NAA, myo-inositol and taurine in the aspalacZ/lacZ brain. Spongy degeneration was prominent in hippocampus, thalamus, brain stem, and cerebellum, whereas white matter of optic nerve and corpus callosum was spared. Intracellular vacuolisation in astrocytes coincides with axonal swellings in cerebellum and brain stem of aspalacZ/lacZ mutants indicating that astroglia may act as an osmolyte buffer in the aspadeficient CNS. In summary, the aspalacZ mouse is an accurate model of CD and an important tool to identify novel aspects of its complex pathology. [ABSTRACT FROM AUTHOR]
Copyright of PLoS ONE is the property of Public Library of Science and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0020336