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Autophagy in neurodegeneration and development
Ashley R. Winslow, David Chaim Rubinsztein
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2008 · ▲ 126 citations
Abstract
Efficient protein turnover is essential for the maintenance of cellular health. Here we review how autophagy(definition) has fundamental functions in cellular homeostasis and possible uses as a therapeutic strategy for neurodegenerative diseases associated with intracytosolic aggregate formation, like Huntington's disease (HD). Drugs like mTOR(definition)-inhibiting drug studied for extending healthspan and lifespan." style="text-decoration:underline dotted; text-underline-offset:2px; cursor:help;">rapamycin(definition), that induce autophagy, increase the clearance of mutant huntingtin fragments and ameliorate the pathology in cell and animal models of HD and related conditions. In Drosophila, the beneficial effects of rapamycin in diseases related to HD are autophagy-dependent. We will also discuss the importance of autophagy in early stages of development and its possible contribution as a secondary disease mechanism in forms of fronto-temporal dementias, motor neuron disease, and lysosomal storage disorders.
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- 10.1016/j.bbadis.2008.06.010
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- 2026-10-22 MST
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APA
Winslow, A.R., & Rubinsztein, D.C. (2008). Autophagy in neurodegeneration and development. <em>Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease</em>. https://doi.org/10.1016/j.bbadis.2008.06.010
Vancouver
Winslow AR, Rubinsztein DC. Autophagy in neurodegeneration and development. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2008. doi:10.1016/j.bbadis.2008.06.010.
BibTeX
@article{ashley2008Autoph,
title = {Autophagy in neurodegeneration and development},
author = {Ashley R. Winslow and David Chaim Rubinsztein},
journal = {Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease},
year = {2008},
doi = {10.1016/j.bbadis.2008.06.010},
}
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