Transmissible spongiform encephalopathiesÂ (TSEs) are rare, but always fatal, neurodegenerative disorders ofÂ humans and other mammals. They are characterized by long incubation periods, spongiform changes in the brain associated with loss of neurons, and the absence of host responses. TSEs are caused by infectious proteins calledÂ prions. Insight into how prions cause TSEs comes from the observation that exposure of neurons to prions causes retraction of dendritic spines (link to paper).
Early alterationsÂ in the nervous system caused by prions include changes in the synapse such asÂ retraction of dendritic spines, the projections where synaptic contacts occur (illustrated;Â image credit). Understanding theseÂ pathologies has been difficult due to a lack of an appropriate neuronal culture system.
To determine if prions are toxic for neurons, primary neuronal cultures were prepared from mice and grown on layers of astrocytes. Addition of an infected brain homogenate from mice that had been inoculated with the scrapie prion, PrPsc, led within 24 hours to retraction of dendritic spines and a reduction in their number and area. Similar effects on dendritic spines were also observed when purified PrPscÂ was used.
No effects of brain homogenates were observed using neurons prepared from mice lacking the prion gene prnp. This observation might have been predicted because prion diseases do not occur in mice lacking the prnp gene. However only anÂ N-terminal domain of PrPcÂ (amino acids 23-31) is required for the loss of dendritic spines.Â It seems likely that this part of PrPcÂ on neurons binds the pathogenic PrPscÂ form, leading to neuronal loss.
Normal prions (PrPc) are completely digested with the enzyme proteinase K, while the pathogenic prionÂ PrPscÂ is relatively resistant. Proteinase K treated PrPscÂ retained the ability to cause retraction of dendritic spines, showing that amino acids 23-90 of the protein are not needed for synaptotoxicity.
Dendritic spines are responsible forÂ excitatory postsynaptic transmission and have roles in learningÂ andÂ memory. Their retraction by pathogenic prions are likely early changes leading to the pathogenic consequences of TSEs. How prions cause spine retractions can now be determined using culturedÂ neurons. It will also be possible to determine if similar mechanisms are involved in dendritic spine loss associated with other neurodegenerative diseases, such asÂ Alzheimer’s, Huntington’s, and Parkinson’s diseases.