Dictyostelium as a model for human disease.
نویسنده
چکیده
Does it make sense to use a simple organism to study human disease? I am sure that all those scientists using non-mammalian models in biomedical research have faced this question many times, perhaps informally in front of the family and friends or in more critical situations under the scrutiny of grant agencies or evaluation committees. There are obvious arguments supported by the history of science telling us the usefulness of learning from simple models and how this has become essential to understand certain pathologies. In addition to the well-known conservation of genes and molecular pathways among distant species there are practical reasons, such as their simplicity and tractability compared with the complexity and the experimental inaccessibility of the human body. An added value from the studies of simple models is that, not infrequently, they open radically new perspectives in the study of a given pathology. This is often the result of applying unbiased genetic analysis and the opportunity in a model organism to address the function of a given gene in the organism as a whole. As a consequence, this research might not be translated immediately to human disease but serve as a ground for more applied approaches. As Louis Pasteur stated “There does not exist a category of science to which one can give the name applied science. There are sciences and the applications of science, bound together as the fruit of the tree which bears it”. This series of reviews exemplifies beautifully howthe social amoeba Dictyostelium fulfills all the requirements for a useful experimental model in understanding the basic principles of human disease.
منابع مشابه
An ancestral non-proteolytic role for presenilin proteins in multicellular development of the social amoeba Dictyostelium discoideum.
Mutations in either of two presenilin genes can cause familial Alzheimer's disease. Presenilins have both proteolysis-dependent functions, as components of the γ-secretase complex, and proteolysis-independent functions in signalling. In this study, we investigate a conserved function of human presenilins in the development of the simple model organism Dictyostelium discoideum. We show that the ...
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The neuronal ceroid lipofuscinoses (NCL) are a group of inherited, severe neurodegenerative disorders also known as Batten disease. Juvenile NCL (JNCL) is caused by recessive loss-of-function mutations in CLN3, which encodes a transmembrane protein that regulates endocytic pathway trafficking, though its primary function is not yet known. The social amoeba Dictyostelium discoideum is increasing...
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Ndufaf5 (also known as C20orf7) is a mitochondrial complex I (CI) assembly factor whose mutations lead to human mitochondrial disease. Little is known about the function of the protein and the cytopathological consequences of the mutations. Disruption of Dictyostelium Ndufaf5 leads to CI deficiency and defects in growth and development. The predicted sequence of Ndufaf5 contains a putative meth...
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Human patients with mitochondrial diseases are more susceptible to bacterial infections, particularly of the respiratory tract. To investigate the susceptibility of mitochondrially diseased cells to an intracellular bacterial respiratory pathogen, we exploited the advantages of Dictyostelium discoideum as an established model for mitochondrial disease and for Legionella pneumophila pathogenesis...
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Lipid droplet formation and subsequent steatosis (the abnormal retention of lipids within a cell) has been reported to contribute to hepatotoxicity and is an adverse effect of many pharmacological agents including the antiepileptic drug valproic acid (VPA). In this study, we have developed a simple model system (Dictyostelium discoideum) to investigate the effects of VPA and related compounds i...
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عنوان ژورنال:
- Seminars in cell & developmental biology
دوره 22 1 شماره
صفحات -
تاریخ انتشار 2011