Journal
NEUROBIOLOGY OF DISEASE
Volume 20, Issue 3, Pages 823-836Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2005.05.018
Keywords
Batten disease; juvenile neuronal ceroid lipofuscinosis; JNCL; CLN3; thalamocortical degeneration; astrocytosis; lysosomal storage disorder
Categories
Funding
- NINDS NIH HHS [R01 NS033648, NS33648, NS41930] Funding Source: Medline
Ask authors/readers for more resources
Juvenile neuronal ceroid lipofuscinosis (JNCL) is the result of mutations in the Cln3 gene. The Cln(3) knock-in mouse (Cln(3)(Delta ex7/8)) reproduces the most common Cln3 mutation and we have now characterized the CNS of these mice at 12 months of age. With the exception of the thalamus, Cln3(Delta ex7/8) homozygotes displayed no significant regional atrophy, but a range of changes in individual laminar thickness that resulted in variable cortical thinning across subfields. Stereological analysis revealed a pronounced loss of. neurons within individual laminae of somatosensory cortex of affected mice and the novel finding of a loss of sensory relay thalamic neurons. These affected mice also exhibited profound astrocytic reactions that were most pronounced in the neocorlex and thalamus, but diminished in other brain regions. These data provide the first direct evidence for neurodegenerative and reactive changes in the thalamocortical system in JNCL and emphasize the localized nature of these events. (c) 2005 Elsevier Inc. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available