Related Experiment Video
Updated: Sep 27, 2026

Visualizing the DNA Damage Response in Purkinje Cells Using Cerebellar Organotypic Cultures
Published on: December 27, 2024
When parsimony backfires: neglecting DNA repair may doom neurons in Alzheimer's disease
Thierry Nouspikel1, Philip C Hanawalt
1Department of Biological Sciences, Stanford University, CA 94305-5020, USA. nouspikel@stanford.edu
Abstract:
Taking advantage of the fact that they need not replicate their DNA, terminally differentiated neurons only repair their expressed genes and largely dispense with the burden of removing damage from most of their genome. However, they may pay a heavy price for this laxity if unforeseen circumstances, such as a pathological condition like Alzheimer's disease, cause them to re-enter the cell cycle. The lifetime accumulation of unrepaired lesions in the silent genes of neurons is likely to be significant and may result in aborting the mitotic process and triggering cell death if the cells attempt to express these dormant genes and resume DNA replication.
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