Acta Neuropathologica

, Volume 120, Issue 5, pp 633–639

Cell type specific sequestration of choline acetyltransferase and tyrosine hydroxylase within Lewy bodies

Original Paper

DOI: 10.1007/s00401-010-0739-1

Cite this article as:
Dugger, B.N. & Dickson, D.W. Acta Neuropathol (2010) 120: 633. doi:10.1007/s00401-010-0739-1


Lewy bodies (LBs), the pathological hallmark of Lewy body disease (LBD), contain α-synuclein, as well as other proteins. In this study, we examined the relationship of α-synuclein to two rate-limiting enzymes in neurotransmitter synthesis, tyrosine hydroxylase (TH) and choline acetyltransferase (ChAT). Double-labeling immunohistochemistry for α-synuclein and TH revealed TH immunoreactivity within LBs in catecholaminergic neurons in the substantia nigra and locus coeruleus, but not within LBs in cholinergic neurons in the pedunculopontine nucleus and nucleus basalis of Meynert. In contrast, ChAT immunoreactivity within LBs was detected in cholinergic, but not within LBs in catecholaminergic neurons. The amygdala was devoid of TH and ChAT positive LBs, although a few Lewy neurites contained ChAT immunoreactivity. Further analysis revealed two distinct patterns of neurotransmitter immunoreactivity within LBs. One pattern had diffuse co-localization of TH or ChAT with α-synuclein as in cortical-type LBs, while the other had intense TH or ChAT immunoreactivity in the LB core surrounded by a peripheral rim of α-synuclein as in brainstem-type LBs. Levels of both TH and ChAT were higher in brainstem-type LBs than in the cytoplasm of the same neuron or in neurons from the same case devoid of LBs. Given the fact that LB-containing neurons have decreases in cytoplasmic TH and ChAT immunoreactivity, these results suggest LBs may disrupt cholinergic and catecholaminergic neurotransmitter production by sequestration of the rate-limiting enzymes for acetylcholine and catecholamine synthesis.


α-Synuclein Choline acetyltransferase Lewy bodies Locus coeruleus Nucleus basalis of Meynert Pedunculopontine nucleus Substantia nigra Tyrosine hydroxylase 

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  1. 1.Neuropathology LaboratoryMayo Clinic College of MedicineJacksonvilleUSA

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