1. Polyploidy in the adult Drosophila brain
- Author
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Shyama Nandakumar, Laura Buttitta, and Olga Grushko
- Subjects
Programmed cell death ,glia ,QH301-705.5 ,DNA damage ,Science ,neurons ,Biology ,medicine.disease_cause ,General Biochemistry, Genetics and Molecular Biology ,Polyploid ,medicine ,Biology (General) ,polyploidy ,General Immunology and Microbiology ,General Neuroscience ,fungi ,endocycles ,General Medicine ,biology.organism_classification ,Cell biology ,Ageing ,Medicine ,Exogenous DNA ,Drosophila melanogaster ,Ploidy ,Developmental biology ,Oxidative stress - Abstract
Long-lived cells such as terminally differentiated postmitotic neurons and glia must cope with the accumulation of damage over the course of an animal’s lifespan. How long-lived cells deal with ageing-related damage is poorly understood. Here we show that polyploid cells accumulate in the ageing adult fly brain and that polyploidy protects against DNA damage-induced cell death. Multiple types of neurons and glia that are diploid at eclosion, become polyploid with age in the adultDrosophilabrain. The optic lobes exhibit the highest levels of polyploidy, associated with an elevated DNA damage response in this brain region with age. Inducing oxidative stress or exogenous DNA damage leads to an earlier onset of polyploidy, and polyploid cells in the adult brain are more resistant to DNA damage-induced cell death than diploid cells. Our results suggest polyploidy may serve a protective role for neurons and glia in ageingDrosophila melanogasterbrains.
- Published
- 2020