Abstract:
:On the basis of the recent cloning of the beta-secretase, the beta-site amyloid precursor protein (APP)-cleaving enzyme (BACE), (Science, 286 (1999) 735), digoxigenin-labelled riboprobes were generated to localize the cellular expression pattern of BACE mRNA in brain sections of transgenic Tg2576 mice, overexpressing the Swedish mutation of the APP695 isoform. Non-radioactive in situ hybridization in combination with immunohistochemistry to identify the cell types and beta-amyloid deposits revealed strong BACE mRNA hybridization signals in neurons of the cerebral cortex, hippocampal formation, thalamus and cholinergic basal forebrain nuclei, while astrocytes did not display any labeling. Neurons surrounding beta-amyloid deposits did not demonstrate altered expression level of BACE mRNA as compared to neurons in cortical areas that are free of beta-amyloid deposits, and the regional expression pattern of BACE mRNA did not correlate with the distribution of beta-amyloid deposits. These data suggest that high level of expression of BACE mRNA is not necessarily related to enhanced deposition of beta-amyloid plaques. To elucidate those factors that contribute to beta-amyloid plaque deposition in a particular region, the transgenic Tg2576 mouse may represent an appropriate tool.
journal_name
Neurosci Lettjournal_title
Neuroscience lettersauthors
Bigl M,Apelt J,Luschekina EA,Lange-Dohna C,Rossner S,Schliebs Rdoi
10.1016/s0304-3940(00)01452-xkeywords:
subject
Has Abstractpub_date
2000-10-06 00:00:00pages
107-10issue
2eissn
0304-3940issn
1872-7972pii
S0304-3940(00)01452-Xjournal_volume
292pub_type
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journal_title:Neuroscience letters
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pub_type: 杂志文章,评审
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pub_type: 杂志文章
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