TY - JOUR
T1 - Alpha-synuclein and tau
T2 - teammates in neurodegeneration?
AU - Moussaud, Simon
AU - Jones, Daryl R.
AU - Moussaud-Lamodière, Elisabeth L.
AU - Delenclos, Marion
AU - Ross, Owen A.
AU - McLean, Pamela J.
N1 - Funding Information:
This work was supported by the Mayo Clinic and the NIH NS063963. OAR is partially supported by NINDS R01# NS078086 and Mayo Clinic Florida is a Morris K. Udall Parkinson's Disease Research Center of Excellence (NINDS P50 #NS072187). The authors would like to thank A.-M. Baine, A. Bradshaw, A. Bronnhuber, Dr. M. Gan, Dr. W. Springer, Dr. F. Fiesel, Dr. C. Labbé, Dr. P. M. Tacik , Dr. M. G. Plumot and Dr. K. F. Bieniek for passionate scientific discussions.
PY - 2014
Y1 - 2014
N2 - The accumulation of α-synuclein aggregates is the hallmark of Parkinson's disease, and more generally of synucleinopathies. The accumulation of tau aggregates however is classically found in the brains of patients with dementia, and this type of neuropathological feature specifically defines the tauopathies. Nevertheless, in numerous cases α-synuclein positive inclusions are also described in tauopathies and vice versa, suggesting a co-existence or crosstalk of these proteinopathies. Interestingly, α-synuclein and tau share striking common characteristics suggesting that they may work in concord. Tau and α-synuclein are both partially unfolded proteins that can form toxic oligomers and abnormal intracellular aggregates under pathological conditions. Furthermore, mutations in either are responsible for severe dominant familial neurodegeneration. Moreover, tau and α-synuclein appear to promote the fibrillization and solubility of each other in vitro and in vivo. This suggests that interactions between tau and α-synuclein form a deleterious feed-forward loop essential for the development and spreading of neurodegeneration. Here, we review the recent literature with respect to elucidating the possible links between α-synuclein and tau.
AB - The accumulation of α-synuclein aggregates is the hallmark of Parkinson's disease, and more generally of synucleinopathies. The accumulation of tau aggregates however is classically found in the brains of patients with dementia, and this type of neuropathological feature specifically defines the tauopathies. Nevertheless, in numerous cases α-synuclein positive inclusions are also described in tauopathies and vice versa, suggesting a co-existence or crosstalk of these proteinopathies. Interestingly, α-synuclein and tau share striking common characteristics suggesting that they may work in concord. Tau and α-synuclein are both partially unfolded proteins that can form toxic oligomers and abnormal intracellular aggregates under pathological conditions. Furthermore, mutations in either are responsible for severe dominant familial neurodegeneration. Moreover, tau and α-synuclein appear to promote the fibrillization and solubility of each other in vitro and in vivo. This suggests that interactions between tau and α-synuclein form a deleterious feed-forward loop essential for the development and spreading of neurodegeneration. Here, we review the recent literature with respect to elucidating the possible links between α-synuclein and tau.
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U2 - 10.1186/1750-1326-9-43
DO - 10.1186/1750-1326-9-43
M3 - Review article
C2 - 25352339
AN - SCOPUS:84964313762
SN - 1750-1326
VL - 9
SP - 43
JO - Molecular neurodegeneration
JF - Molecular neurodegeneration
ER -