Selective expression of α-synuclein-immunoreactivity in vesicular acetylcholine transporter-immunoreactive axons in the guinea pig rectum and human colon

J Comp Neurol. 2013 Feb 15;521(3):657-76. doi: 10.1002/cne.23198.

Abstract

Parkinson's disease is a neurodegenerative disorder characterized by motor and nonmotor impairments, including constipation. The hallmark pathological features of Parkinson's disease are Lewy bodies and neurites, of which aggregated α-synuclein is a major constituent. Frequently, Lewy pathology is identified in the distal gut of constipated Parkinson's disease patients. The neurons that innervate the distal gut that express α-synuclein have not been identified. We used multiple-labeling immunohistochemistry and anterograde tracing to quantify which neurons projecting to the guinea pig rectum and human colon expressed α-synuclein in their axons. α-Synuclein-immunoreactivity was present in 24 ± 0.7% of somatostatin (SOM)-immunoreactive (IR) varicosities; 20 ± 4.3% of substance P (SP)-IR varicosities and 9 ± 1.3% vasoactive intestinal polypeptide (VIP)-IR varicosities in guinea pig rectal myenteric ganglia. However, α-synuclein-immunoreactivity was localized in significantly more vesicular acetylcholine transporter (VAChT)-IR varicosities (88 ± 3%, P < 0.001). Of SOM-IR, SP-IR, and VIP-IR varicosities that lacked VAChT-immunoreactivity, only 1 ± 0.3%, 0 ± 0.3%, and 0% contained α-synuclein-immunoreactivity, respectively. 71 ± 0.8% of VAChT-IR varicosities in myenteric ganglia of human colon were α-synuclein-IR. In guinea pig rectal myenteric ganglia, α-synuclein- and VAChT-immunoreactivity coexisted in 15 ± 1.4% of biotinamide-labeled extrinsic varicosities; only 1 ± 0.3% of biotinamide-labeled extrinsic varicosities contained α-synuclein-immunoreactivity without VAChT-immunoreactivity. α-Synuclein expression in axons to the distal gut correlates closely with expression of the cholinergic marker, VAChT. This is the first report of cell-selective α-synuclein expression in the nervous system. Our results suggest cholinergic neurons in the gut may be vulnerable in Parkinson's disease.

MeSH terms

  • Adult
  • Aged
  • Animals
  • Antibody Specificity
  • Axons / metabolism
  • Axons / pathology
  • Cholinergic Neurons / metabolism
  • Cholinergic Neurons / pathology
  • Colon / innervation
  • Constipation / etiology
  • Constipation / metabolism*
  • Constipation / pathology
  • Female
  • Guinea Pigs
  • Humans
  • Immunohistochemistry / standards
  • Lewy Bodies / metabolism
  • Lewy Bodies / pathology
  • Male
  • Middle Aged
  • Myenteric Plexus / metabolism*
  • Myenteric Plexus / pathology
  • Parkinson Disease / complications
  • Parkinson Disease / metabolism*
  • Parkinson Disease / pathology
  • Rectum / innervation
  • Reproducibility of Results
  • Vesicular Acetylcholine Transport Proteins / immunology
  • Vesicular Acetylcholine Transport Proteins / metabolism*
  • alpha-Synuclein / immunology
  • alpha-Synuclein / metabolism*

Substances

  • SLC18A3 protein, human
  • SNCA protein, human
  • Vesicular Acetylcholine Transport Proteins
  • alpha-Synuclein