Dictyostelium discoideum as a Model for Investigating Neurodegenerative Diseases
Open Access
- 27 October 2021
- journal article
- review article
- Published by Frontiers Media SA in Frontiers in Cellular Neuroscience
- Vol. 15
Abstract
The social amoeba Dictyostelium discoideum is a model organism that is used to investigate many cellular processes including chemotaxis, cell motility, cell differentiation, and human disease pathogenesis. While many single-cellular model systems lack homologs of human disease genes, Dictyostelium’s genome encodes for many genes that are implicated in human diseases including neurodegenerative diseases. Due to its short doubling time along with the powerful genetic tools that enable rapid genetic screening, and the ease of creating knockout cell lines, Dictyostelium is an attractive model organism for both interrogating the normal function of genes implicated in neurodegeneration and for determining pathogenic mechanisms that cause disease. Here we review the literature involving the use of Dictyostelium to interrogate genes implicated in neurodegeneration and highlight key questions that can be addressed using Dictyostelium as a model organism.Keywords
This publication has 188 references indexed in Scilit:
- The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative diseaseBrain Research, 2012
- The dynamic cytoskeleton: backbone of dendritic spine plasticityCurrent Opinion in Neurobiology, 2011
- L10p and P158DEL DJ‐1 mutations cause protein instability, aggregation, and dimerization impairmentsJournal of Neuroscience Research, 2010
- Leucine-rich repeat kinase 2 induces α-synuclein expression via the extracellular signal-regulated kinase pathwayCellular Signalling, 2010
- Prions, protein homeostasis, and phenotypic diversityTrends in Cell Biology, 2010
- Neurodegenerative diseases: Lessons from genome‐wide screens in small model organismsEMBO Molecular Medicine, 2009
- A Systematic Survey Identifies Prions and Illuminates Sequence Features of Prionogenic ProteinsCell, 2009
- Wild-type LRRK2 but not its mutant attenuates stress-induced cell death via ERK pathwayNeurobiology of Disease, 2008
- Mitochondrial Medicine for Aging and Neurodegenerative DiseasesNeuroMolecular Medicine, 2008
- Amyloid beta, mitochondrial dysfunction and synaptic damage: implications for cognitive decline in aging and Alzheimer's diseaseTrends in Molecular Medicine, 2008