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. 2017 Nov;1863(11):2762–2771. doi: 10.1016/j.bbadis.2017.07.007

Table 1.

Examples of misfolding proteins involved in neurodegenerative diseases that undergo cell-to-cell transfer in different conditioned medium experimental set ups. N.A., not applicable, N.C., not characterised.

Experimental set up Protein of interest Disease Transferring species Cell line
Membrane barrier Dipeptide repeat proteins from C9orf72 hexanucleotide repeat expansions ALS N.C. NSC-34 [51]
SOD1 ALS N.C. Neuro 2 A [45]
Application onto acceptor culture Tau Alzheimer's N.C [80].,
Fibrils [81]
HEK293 [80],
Primary neurons [81]
Huntingtin (Q19 and Q103) Huntington's N.C. HEK donors and SH-SY5Y acceptors [82]
α-Synuclein Parkinson's Monomers, oligomers and fibrils [83]
High and low molecular weight oligomers [84]
SH-SY5Y donors and COS-7 acceptors [83]
Differentiated and undifferentiated SH-SY5Y [84]
SOD1 ALS N.C [45]. Neuro 2 A [45]
TDP-43 ALS N.C. HEK293 [27], [74]
Exosome isolation Yeast prion Sup35 (NM domain) N.A. Multimers [85]
N.C [86].
Neuro2A [85], [86]
SOD1 ALS N.C. NSC-34 [66]
Complementary protein assay model Tau Alzheimer's N.C. HEK293T [87]
TDP-43 ALS Dimers, oligomers HEK293 [75]