GM1-Ganglioside-Mediated Activation of the Unfolded Protein Response Causes Neuronal Death in a Neurodegenerative Gangliosidosis

• Published in: Molecular cell Vol. 15; no. 5; pp. 753 - 766
• Main Authors: Tessitore, Alessandra, del P. Martin, Maria, Sano, Renata, Ma, Yanjun, Mann, Linda, Ingrassia, Angela, Laywell, Eric D., Steindler, Dennis A., Hendershot, Linda M., d'Azzo, Alessandra
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 10-09-2004
• Subjects: Animals; Animals, Newborn; Apoptosis - genetics; beta-Galactosidase - deficiency; beta-Galactosidase - genetics; Calcium - metabolism; Caspase 12; Caspases - metabolism; CCAAT-Enhancer-Binding Proteins - metabolism; Cell Death - genetics; Cells, Cultured; Disease Models, Animal; Endoplasmic Reticulum Chaperone BiP; G(M1) Ganglioside - metabolism; Gangliosidosis, GM1 - genetics; Gangliosidosis, GM1 - metabolism; Gangliosidosis, GM1 - physiopathology; Heat-Shock Proteins - metabolism; Mice; Mice, Knockout; Mitogen-Activated Protein Kinase 9; Mitogen-Activated Protein Kinases - metabolism; Molecular Chaperones - metabolism; N-Acetylgalactosaminyltransferases - metabolism; Nerve Degeneration - genetics; Nerve Degeneration - metabolism; Nerve Degeneration - physiopathology; Neurons - metabolism; Neurons - pathology; Polypeptide N-acetylgalactosaminyltransferase; Protein Folding; Transcription Factor CHOP; Transcription Factors - metabolism
• ISSN: 1097-2765; 1097-4164
• DOI: 10.1016/j.molcel.2004.08.029

GM1-ganglioside (GM1) is a major sialoglycolipid of neuronal membranes that, among other functions, modulates calcium homeostasis. Excessive accumulation of GM1 due to deficiency of lysosomal β-galactosidase (β-gal) characterizes the neurodegenerative disease GM1-gangliosidosis, but whether the accumulation of GM1 is directly responsible for CNS pathogenesis was unknown. Here we demonstrate that activation of an unfolded protein response (UPR) associated with the upregulation of BiP and CHOP and the activation of JNK2 and caspase-12 leads to neuronal apoptosis in the mouse model of GM1-gangliosidosis. GM1 loading of wild-type neurospheres recapitulated the phenotype of β-gal−/− cells and activated this pathway by depleting ER calcium stores, which ultimately culminated in apoptosis. Activation of UPR pathways did not occur in mice double deficient for β-gal and ganglioside synthase, β-gal−/−/GalNAcT−/−, which do not accumulate GM1. These findings suggest that the UPR can be induced by accumulation of the sialoglycolipid GM1 and this causes a novel mechanism of neuronal apoptosis.