Novel Neuroprotective Function of Apical-Basal Polarity Gene Crumbs in Amyloid Beta 42 (A beta 42) Mediated Neurodegeneration: e78717

• Published in: PloS one Vol. 8; no. 11
• Main Authors: Steffensmeier, Andrew M, Tare, Meghana, Puli, Oorvashi Roy, Modi, Rohan, Nainaparampil, Jaison, Kango-Singh, Madhuri, Singh, Amit
• Format: Journal Article
• Language: English
• Published: 01.11.2013
• Subjects: Alzheimer's disease; Drosophila
• ISSN: 1932-6203
• DOI: 10.1371/journal.pone.0078717

Alzheimer's disease (AD, OMIM: 104300), a progressive neurodegenerative disorder with no cure to date, is caused by the generation of amyloid-beta-42 (A beta 42) aggregates that trigger neuronal cell death by unknown mechanism(s). We have developed a transgenic Drosophila eye model where misexpression of human A beta 42 results in AD-like neuropathology in the neural retina. We have identified an apical-basal polarity gene crumbs (crb) as a genetic modifier of A beta 42-mediated-neuropathology. Misexpression of A beta 42 caused upregulation of Crb expression, whereas downregulation of Crb either by RNAi or null allele approach rescued the A beta 42-mediated-neurodegeneration. Co-expression of full length Crb with A beta 42 increased severity of A beta 42-mediated-neurodegeneration, due to three fold induction of cell death in comparison to the wild type. Higher Crb levels affect axonal targeting from the retina to the brain. The structure function analysis identified intracellular domain of Crb to be required for A beta 42-mediated-neurodegeneration. We demonstrate a novel neuroprotective role of Crb in A beta 42-mediated-neurodegeneration.