Synucleinopathies

Synucleinopathies (also called α-Synucleinopathies) are neurodegenerative diseases characterised by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibres or glial cells.[1] One prevailing hypothesis has been that the death of dopaminergic cells is the proximate cause of functional deficits.[2] However, introduction of exogenous α-SYN in a rodent animal model has been shown to induce functional deficits preceding cell death.[2]

There are three main types of synucleinopathy: Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy.[1] Other rare disorders, such as various neuroaxonal dystrophies, also have α-synuclein pathologies.[1]

Positive α-Synuclein staining of a Lewy body in a patient with Parkinson's disease.

Because each of the synucleinopathies has a distinct set of symptoms, prognosis and management issues, it has been suggested that the term "has little practical value as a diagnostic term for the clinician."[3]

Synucleinopathies can sometimes overlap with tauopathies, possibly because of interaction between the synuclein and tau proteins.[4][5]

See also

References

  1. 1 2 3 McCann, H; Stevens, C. H.; Cartwright, H; Halliday, G. M. (2014). "Α-Synucleinopathy phenotypes". Parkinsonism & Related Disorders. 20 Suppl 1: S62–7. doi:10.1016/S1353-8020(13)70017-8. PMID 24262191.
  2. 1 2 Peelaerts W, Bousset L, Van der Perren A, et al. (Jun 2015). "α-Synuclein strains cause distinct synucleinopathies after local and systemic administration". Nature. advance online publication. doi:10.1038/nature14547. Lay summary KU Leuven (2015).
  3. Martí MJ, Tolosa E, Campdelacreu J. (Sep 2003). "Clinical overview of the synucleinopathies". Movement Disorders. 18 (Suppl 6): S21–7. doi:10.1002/mds.10559. PMID 14502652.
  4. Simon Moussaud, Daryl R Jones, Elisabeth L Moussaud-Lamodière, Marion Delenclos, Owen A Ross, and Pamela J McLean, corresponding author (October 2014). "Alpha-synuclein and tau: teammates in neurodegeneration?". Mol Neurodegener. doi:10.1186/1750-1326-9-43. PMC 4230508Freely accessible. PMID 25352339.
  5. Jing L. Guo,1 Dustin J. Covell,1 Joshua P. Daniels,1 Michiyo Iba,1 Anna Stieber,1 Bin Zhang,1 Dawn M. Riddle,1 Linda K. Kwong,1 Yan Xu,1 John Q. Trojanowski,1 and Virginia M.Y. Lee1,* (July 2013). "Distinct α-Synuclein Strains Differentially Promote Tau Inclusions in Neurons". Cell. 154 (1): 103–17. doi:10.1016/j.cell.2013.05.057. PMC 3820001Freely accessible. PMID 23827677.
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