Table 1.
Potential candidate disease-associated transmissible proteins.
| Disease | Protein (location) | Experimental Transmission | Natural Transmission | References* |
|---|---|---|---|---|
| Prion diseases | PrPSc (extracellular) | Infectious in diverse animal species by various routes | Infectious in diverse species by various routes | (Prusiner, 1998; Aguzzi and Calella, 2009) |
| Alzheimer's disease | Aβ (extracellular) | Induction of pathology in transgenic mice by intracerebral and intraperiotoneal inoculation | Not shown | (Kane et al., 2000; Meyer-Luehmann et al., 2006; Eisele et al., 2010; Morales et al., 2011) |
| Parkinson's disease | α-synuclein (cytoplasmatic) | Cell-to-cell and host-to-graft spreading in animal models | Host-to-graft spreading in humans | (Desplats et al., 2009; Luk et al., 2009; Volpicelli-Daley et al., 2011; Mougenot et al., 2011; Hansen et al., 2011) |
| Huntington's disease | Huntingtin (nuclear) | Cell-to-cell spreading in culture | Not shown | (Ren et al., 2009) |
| Tauopathies | Tau (cytoplasmatic) | Cell-to-cell spreading in culture and transmission in transgenic mice by intracerebral inoculation | Not shown | (Clavaguera et al., 2009; Frost et al., 2009; Nonaka et al., 2010; Guo and Lee, 2011) |
| Secondary amyloidosis | Amyloid-A (extracellular) | Acceleration of pathology in mice by various routes of administration | Possible transmission to captive cheetah | (Lundmark et al., 2002; Zhang et al., 2008) |
| Mouse senile amyloidosis | Apolipoprotein A (extracellular) | Acceleration of pathology in mice by various routes of administration | Transmission to mice in the same cage by feces consumption | (Xing et al., 2001; Korenaga et al., 2006) |
There are several more references that could have been cited, but for space constraints only the most relevant articles are listed.