Previous work in our laboratory determined that a relentless inflammatory response in the CNS preceded the onset of symptoms in the Sandhoff mouse, an authentic model of infantile Tay-Sachs and Sandhoff disease. Specifically we found that inflammatory proteins including TNF-a, IL-1b and MIP1-a precede the onset of neuronal apoptosis and clinical decline. In addition, the accumulation of GM1 or GM2 ganglioside in the brain parenchyma of GM1 and GM2 gangliosidosis patients, respectively, has long been known to be a hallmark of these diseases? ? We are currently conducting a natural history study (Protocol 02-DK-0107, Investigation of Neurodegeneration in the Glycopshingolipid Storage Disorders) to investigate the expression of inflammatory proteins and quantitate GM1 and GM2 ganglioside in the CNS of children with GSL storage diseases and to correlate them with neurodegenerative changes as assessed by magnetic resonance imaging and clinical disease progression.

Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2007
Total Cost
$303,244
Indirect Cost
City
State
Country
United States
Zip Code
Wu, Yun-Ping; Mizugishi, Kiyomi; Bektas, Meryem et al. (2008) Sphingosine kinase 1/S1P receptor signaling axis controls glial proliferation in mice with Sandhoff disease. Hum Mol Genet 17:2257-64
Kono, Mari; Allende, Maria Laura; Proia, Richard L (2008) Sphingosine-1-phosphate regulation of mammalian development. Biochim Biophys Acta 1781:435-41