Brain gangliosides of a transgenic mouse model of Alzheimer's disease with deficiency in GD3-synthase: Expression of elevated levels of a cholinergic-specific ganglioside, GT1aα
- Toshio Ariga,
- ,
- Michael P. McDonald,
- Yoshio Hirabayashi,
- Susumu Ando,
- Robert K Yu
- Augusta University,
- VA Medical Center,
- University of Tennessee Health Science Center,
- Brain Science Institute,
- Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology,
Open access
Abstract
In order to examine the potential involvement of gangliosides in AD (Alzheimer's disease), we compared the ganglioside compositions of the brains of a double-transgenic (Tg) mouse model [APP (amyloid precursor protein)/PSEN1 (presenilin)] of AD and a triple mutant mouse model with an additional deletion of the GD3S (GD3-synthase) gene (APP/PSEN1/GD3S-/-). These animals were chosen since it was previously reported that APP/PSEN1/GD3S-/- triplemutant mice performed as well as WT (wild-type) control and GD3S-/- mice on a number of reference memory tasks. Cholinergic neuron-specific gangliosides, such as GT1aα and GQ1bα, were elevated in the brains of double-Tg mice (APP/PSEN1), as compared with those of WT mice. Remarkably, in the triple mutant mouse brains (APP/PSEN1/GD3S-/-), the concentration of GT1aα was elevated and as expected there was no expression of GQ1bα. On the other hand, the level of c-series gangliosides, including GT3, was significantly reduced in the double-Tg mouse brain as compared with the WT. Thus, the disruption of the gene of a specific ganglioside-synthase, GD3S, altered the expression of cholinergic neuron-specific gangliosides. Our data thus suggest the intriguing possibility that the elevated cholinergic-specific ganglioside, GT1aα, in the triple mutant mouse brains (APP/PSEN1/GD3S-/-) may contribute to the memory retention in these mice.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 141-148 (8 pages)Journal (Volume, Issue Number)
ASN Neuro (Volume 5, Issue 2)Publication milestones
- Published - 2013
Publication status
ISSN
1759-0914Publication IDs
- Scopus: 84880980912
- PubMed: 23565921
