Prion strains depend on different endocytic routes for productive infection.

Prion strains depend on different endocytic routes for productive infection.
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DOI:
10.1038/s41598-017-07260-2
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发表时间:
2017-07-31
期刊:
影响因子:
4.6
通讯作者:
Vorberg IM
Vorberg IM
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Fehlinger A;Wolf H;Hossinger A;Duernberger Y;Pleschka C;Riemschoss K;Liu S;Bester R;Paulsen L;Priola SA;Groschup MH;Schätzl HM;Vorberg IM

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Prions are unconventional agents composed of misfolded prion protein that cause fatal neurodegenerative diseases in mammals. Prion strains induce specific neuropathological changes in selected brain areas. The mechanism of strain-specific cell tropism is unknown. We hypothesised that prion strains rely on different endocytic routes to invade and replicate within their target cells. Using prion permissive cells, we determined how impairment of endocytosis affects productive infection by prion strains 22L and RML. We demonstrate that early and late stages of prion infection are differentially sensitive to perturbation of clathrin- and caveolin-mediated endocytosis. Manipulation of canonical endocytic pathways only slightly influenced prion uptake. However, blocking the same routes had drastic strain-specific consequences on the establishment of infection. Our data argue that prion strains use different endocytic pathways for infection and suggest that cell type-dependent differences in prion uptake could contribute to host cell tropism.