Prions Link Cholesterol To Neurodegeneration
Main Category: Neurology / NeuroscienceAlso Included In: Cholesterol; Biology / Biochemistry; Infectious Diseases / Bacteria / Viruses
Article Date: 12 Feb 2008 - 2:00 PDT
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Prion infection of neurons increases the free cholesterol content in cell membranes. A new study published in the online open access journal BMC Biology suggests that disturbances in membrane cholesterol may be the mechanism by which prions cause neurodegeneration and could point to a role for cholesterol in other neurodegenerative diseases.
It is widely believed that prions (protein only infectious material) are the cause of rare progressive neurodegenerative disorders that affect both humans and animals. A prion is an infectious agent made solely of protein. However what is not known is how the prions damage brain cells (neurons).
Dr Clive Bate and colleagues from the Royal Veterinary College in the UK compared the amounts of protein and cholesterol in prion-infected neuronal cell lines and primary cortical neurons with uninfected controls. Protein levels were similar but the amount of total cholesterol (a mixture of free and esterified cholesterol) was significantly higher in the infected cell lines. The cholesterol balance was also affected: the amount of free cholesterol increased but that of cholesterol esters reduced, suggesting that prion infection affects cholesterol regulation. The team attempted to reproduce the effects of prions on cholesterol levels, by stimulating cholesterol biosynthesis or by adding exogenous cholesterol. Both approaches resulted in increased amounts of cholesterol esters but not of free cholesterol. The free cholesterol is thought to affect the function of the cell membranes and to lead to abnormal activation of phospholipase A2, an enzyme implicated in the depletion of neurons in prion and Alzheimer's disease.
Studies have recently shown that the controlling cholesterol levels within the brain is critical in limiting the development of neurodegenerative diseases such as Alzheimer's, Parkinson's and prion diseases, multiple sclerosis, and senile dementia. This study now gives far more specific insight into the kind of mechanisms at work. Dr Bate stated: "Our observations raise the possibility that disturbances in membrane cholesterol induced by prions are major triggering events in the neuropathogenesis of prion diseases".
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Article adapted by Medical News Today from original press release.
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1. Sequestration of free cholesterol in cell membranes by prions correlates with cytoplasmic phospholipase A2 activation
Clive Bate, Mourad Tayebi and Alun Williams
BMC Biology (in press)
Article available at BMC Biology journal website: http://www.biomedcentral.com/bmcbiol/
All articles are available free of charge, according to BioMed Central's open access policy.
2. BMC Biology - the flagship biology journal of the BMC series - publishes research and methodology articles of special importance and broad interest in any area of biology and biomedical sciences. BMC Biology (ISSN 1741-7007) is covered by PubMed, MEDLINE, BIOSIS, CAS, Scopus, EMBASE, Zoological Record, Thomson Scientific (ISI) and Google Scholar. The journal will receive its first Impact Factor in 2008.
3. BioMed Central (http://www.biomedcentral.com/) is an independent online publishing house committed to providing immediate access without charge to the peer-reviewed biological and medical research it publishes. This commitment is based on the view that open access to research is essential to the rapid and efficient communication of science.
4. The Royal Veterinary College is the UK's first and largest veterinary school and a constituent College of the University of London. The College is one of the leading veterinary research centres in Europe and received 5 out of 5 in the latest Research Assessment Exercise. It also provides support for veterinary and related professions through its three referral hospitals, diagnostic services and continuing professional development courses. http://www.rvc.ac.uk
Source: Charlotte Webber
BioMed Central
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