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. Author manuscript; available in PMC: 2013 May 25.
Published in final edited form as: Cell. 2012 May 25;149(5):968–977. doi: 10.1016/j.cell.2012.05.007

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.