24S-hydroxycholesterol: cellular effects and variations in brain diseases
Abstract The adult brain exhibit a characteristic cholesterol homeostasis, with low synthesis rate and active catabolism. Brain cholesterol turnover is possible thanks to the action of the enzyme Cytochrome P450 46A1 (CYP46A1) or 24-cholesterol hydroxylase, that transforms cholesterol into 24S-h...
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| Formato: | Artículo |
| Lenguaje: | Inglés |
| Publicado: |
Wiley
2020
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| Acceso en línea: | https://repositorio.uca.edu.ar/handle/123456789/10916 |
| Aporte de: |
| Sumario: | Abstract
The adult brain exhibit a characteristic cholesterol homeostasis, with low synthesis rate and
active catabolism. Brain cholesterol turnover is possible thanks to the action of the enzyme
Cytochrome P450 46A1 (CYP46A1) or 24-cholesterol hydroxylase, that transforms cholesterol into
24S-hydroxycholesterol (24S-HC). But before crossing the blood-brain barrier (BBB), this oxysterol
that is the most abundant in the brain can act locally, affecting the functioning of neurons, astrocytes,
oligodendrocytes, and vascular cells. The first part of this review addresses different aspects of 24SHC production and elimination from the brain. The second part concentrates in the effects of 24S-HC
at the cellular level, describing how this oxysterol affects cell viability, amyloid β production,
neurotransmission, and transcriptional activity. Finally, the role of 24S-HC in Alzheimer, Huntington
and Parkinson diseases, multiple sclerosis and amyotrophic lateral sclerosis, as well as the possibility
of using this oxysterol as predictive and/or evolution biomarker in different brain disorders is
discussed. |
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