Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated a-synuclein gene mutations precede central nervous system changes

• Published in: Human molecular genetics Vol. 19; no. 9; pp. 1633 - 1650
• Main Authors: Kuo, Yien-Ming, Li, Zhishan, Jiao, Yun, Gaborit, Nathalie, Pani, Amar K, Orrison, Bonnie M, Bruneau, Benoit G, Giasson, Benoit I, Smeyne, Richard J, Gershon, Michael D, Nussbaum, Robert L
• Format: Journal Article
• Language: English
• Published: 01.05.2010
• ISSN: 0964-6906; 1460-2083
• DOI: 10.1093/hmg/ddq038

Parkinson disease (PD) is a neurodegenerative disease with motor as well as non-motor signs in the gastrointestinal tract that include dysphagia, gastroparesis, prolonged gastrointestinal transit time, constipation and difficulty with defecation. The gastrointestinal dysfunction commonly precedes the motor symptoms by decades. Most PD is sporadic and of unknown etiology, but a fraction is familial. Among familial forms of PD, a small fraction is caused by missense (A53T, A30P and E46K) and copy number mutations in SNCA which encodes a-synuclein, a primary protein constituent of Lewy bodies, the pathognomonic protein aggregates found in neurons in PD. We set out to develop transgenic mice expressing mutant a-synuclein (either A53T or A30P) from insertions of an entire human SNCA gene as models for the familial disease. Both the A53T and A30P lines show robust abnormalities in enteric nervous system (ENS) function and synuclein-immunoreactive aggregates in ENS ganglia by 3 months of age. The A53T line also has abnormal motor behavior but neither demonstrates cardiac autonomic abnormalities, olfactory dysfunction, dopaminergic neurotransmitter deficits, Lewy body inclusions or neurodegeneration. These animals recapitulate the early gastrointestinal abnormalities seen in human PD. The animals also serve as an in vivo system in which to investigate therapies for reversing the neurological dysfunction that target a-synuclein toxicity at its earliest stages.