TY - JOUR
T1 - Virus-induced alterations of membrane lipids affect the incorporation of PrPSc into cells
AU - Avrahami, Dana
AU - Dayan-Amouyal, Yael
AU - Tal, Saar
AU - Mincberg, Michal
AU - Davis, Claytus
AU - Abramsky, Oded
AU - Gabizon, Ruth
PY - 2008
Y1 - 2008
N2 - Prion diseases are fatal neurodegenerative disorders characterized by long incubation periods. To investigate whether concurrent diseases can modify the clinical outcome of prion-affected subjects, we tested the effect of viral infection on the binding and internalization of PrPSc, essential steps of prion propagation. To this effect, we added scrapie brain homogenate or purified PrPSc to fibroblasts previously infected with minute virus of mice (MVM), a mouse parvovirus. We show here that the rate of incorporation of PrPSc into MVM-infected cells was significantly higher than that observed for naïve cells. Immunostaining of cells and immunoblotting of subcellular fractions using antibodies recognizing PrP and Lyso-Tracker, a lysosomal marker, revealed that in both control and MVM-infected cells the incorporated PrPSc was associated mostly with lysosomes. Interestingly, floatation gradient analysis revealed that the majority of the PrPSc internalized into MVM-infected cells shifted toward raft-containing low-density fractions. Concomitantly, the MVM-infected cells demonstrated increased levels of the glycosphingolipid GM1 (an essential raft lipid component) throughout the gradient and a shift in caveolin 1 (a raft protein marker) toward lighter membrane fractions compared with noninfected cells. Our results suggest that the effect of viral infection on membrane lipid composition may promote the incorporation of exogenous PrPSc into rafts. Importantly, membrane rafts are believed to be the conversion site of PrPC to PrPSc; therefore, the association of exogenous PrPSc with such membrane microdomains may facilitate prion infection.
AB - Prion diseases are fatal neurodegenerative disorders characterized by long incubation periods. To investigate whether concurrent diseases can modify the clinical outcome of prion-affected subjects, we tested the effect of viral infection on the binding and internalization of PrPSc, essential steps of prion propagation. To this effect, we added scrapie brain homogenate or purified PrPSc to fibroblasts previously infected with minute virus of mice (MVM), a mouse parvovirus. We show here that the rate of incorporation of PrPSc into MVM-infected cells was significantly higher than that observed for naïve cells. Immunostaining of cells and immunoblotting of subcellular fractions using antibodies recognizing PrP and Lyso-Tracker, a lysosomal marker, revealed that in both control and MVM-infected cells the incorporated PrPSc was associated mostly with lysosomes. Interestingly, floatation gradient analysis revealed that the majority of the PrPSc internalized into MVM-infected cells shifted toward raft-containing low-density fractions. Concomitantly, the MVM-infected cells demonstrated increased levels of the glycosphingolipid GM1 (an essential raft lipid component) throughout the gradient and a shift in caveolin 1 (a raft protein marker) toward lighter membrane fractions compared with noninfected cells. Our results suggest that the effect of viral infection on membrane lipid composition may promote the incorporation of exogenous PrPSc into rafts. Importantly, membrane rafts are believed to be the conversion site of PrPC to PrPSc; therefore, the association of exogenous PrPSc with such membrane microdomains may facilitate prion infection.
KW - MVM
KW - Prions
KW - Rafts
UR - http://www.scopus.com/inward/record.url?scp=57049109793&partnerID=8YFLogxK
U2 - 10.1002/jnr.21720
DO - 10.1002/jnr.21720
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C2 - 18478553
AN - SCOPUS:57049109793
SN - 0360-4012
VL - 86
SP - 2753
EP - 2762
JO - Journal of Neuroscience Research
JF - Journal of Neuroscience Research
IS - 12
ER -