Apoptotic death induces Abeta production and fibril formation to a much larger extent than necrotic-like death in CGNs.

In this study we report that apoptotic death of primary cultures of cerebellar granule neurons is accompanied by release of thioflavin-binding proteins - indicative of the presence of beta-sheet structures - and fibril formation in the culture medium. When the same neurons are subjected to an excytotoxic death caused by 100 microM glutamate exposure, the amount of thioflavin binding is markedly reduced. Western blot analysis shows that fibrils contain monomers, dimers and trimers of amyloid-beta (Abeta) which, when observed at the electron microscope, have morphologies reminiscent of fibrils of senile plaques. These findings demonstrate that triggering an apoptotic pathway leads to beta-sheet transition and fibril formation of a protein primarily involved in Alzheimer's disease and may be of direct relevance to the possible link between apoptosis and this neuropathology.

[1]  H. Wootz,et al.  ER stress and neurodegenerative diseases , 2006, Cell Death and Differentiation.

[2]  M. Costanzi,et al.  NMDA receptor mediates tau-induced neurotoxicity by calpain and ERK/MAPK activation. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[3]  E. Mackenzie,et al.  NMDA Receptor Activation Inhibits α-Secretase and Promotes Neuronal Amyloid-β Production , 2005, The Journal of Neuroscience.

[4]  S. Westerheide,et al.  Heat Shock Response Modulators as Therapeutic Tools for Diseases of Protein Conformation* , 2005, Journal of Biological Chemistry.

[5]  Adriana B Ferreira,et al.  The Generation of a 17 kDa Neurotoxic Fragment: An Alternative Mechanism by which Tau Mediates β-Amyloid-Induced Neurodegeneration , 2005, The Journal of Neuroscience.

[6]  Nektarios Tavernarakis,et al.  Proteolytic mechanisms in necrotic cell death and neurodegeneration , 2005, FEBS letters.

[7]  M. Moskowitz,et al.  Exciting, radical, suicidal: how brain cells die after stroke. , 2005, Stroke.

[8]  D. Selkoe,et al.  Cell biology of protein misfolding: The examples of Alzheimer's and Parkinson's diseases , 2004, Nature Cell Biology.

[9]  D. Dickson Apoptotic mechanisms in Alzheimer neurofibrillary degeneration: cause or effect? , 2004, The Journal of clinical investigation.

[10]  C. Ross,et al.  Protein aggregation and neurodegenerative disease , 2004, Nature Medicine.

[11]  C. Cotman,et al.  Caspase-cleavage of tau is an early event in Alzheimer disease tangle pathology. , 2004, The Journal of clinical investigation.

[12]  Alexei Degterev,et al.  Diversity in the Mechanisms of Neuronal Cell Death , 2003, Neuron.

[13]  M. Tymianski,et al.  Molecular mechanisms of calcium-dependent neurodegeneration in excitotoxicity. , 2003, Cell calcium.

[14]  R. Berry,et al.  Caspase cleavage of tau: Linking amyloid and neurofibrillary tangles in Alzheimer's disease , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[15]  S Rabe-Hesketh,et al.  Head injury as a risk factor for Alzheimer’s disease: the evidence 10 years on; a partial replication , 2003, Journal of neurology, neurosurgery, and psychiatry.

[16]  M. Ciotti,et al.  Transfer of the apoptotic message in sister cultures of cerebellar neurons , 2001, Neuroreport.

[17]  D. R. Kaplan,et al.  Neurotrophin signalling pathways regulating neuronal apoptosis , 2001, Cellular and Molecular Life Sciences CMLS.

[18]  David Smith,et al.  Involvement of Caspases in Proteolytic Cleavage of Alzheimer’s Amyloid-β Precursor Protein and Amyloidogenic Aβ Peptide Formation , 1999, Cell.

[19]  C. Barbato,et al.  Tau Cleavage and Dephosphorylation in Cerebellar Granule Neurons Undergoing Apoptosis , 1998, The Journal of Neuroscience.

[20]  E. Gratton,et al.  Prodan as a membrane surface fluorescence probe: partitioning between water and phospholipid phases. , 1998, Biophysical journal.

[21]  M. Ciotti,et al.  Increased amyloidogenic secretion in cerebellar granule cells undergoing apoptosis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[22]  C. Finch,et al.  Evidence for Apoptotic Cell Death in Alzheimer's Disease , 1995, Experimental Neurology.

[23]  Antonella,et al.  Apoptosis in cerebellar granule cells is blocked by high KCl, forskolin, and IGF-1 through distinct mechanisms of action: the involvement of intracellular calcium and RNA synthesis , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[24]  Brian J Cummings,et al.  Immunohistochemical evidence for apoptosis in Alzheimer's disease. , 1994, Neuroreport.

[25]  S. D’Mello,et al.  Induction of apoptosis in cerebellar granule neurons by low potassium: inhibition of death by insulin-like growth factor I and cAMP. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[26]  L. Battistini,et al.  Recombinant human insulin-like growth factor I exerts a trophic action and confers glutamate sensitivity on glutamate-resistant cerebellar granule cells. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[27]  C. Cotman,et al.  Apoptosis is induced by beta-amyloid in cultured central nervous system neurons. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[28]  J. Kabat,et al.  Molecular characterization of the minimal protease resistant tau unit of the Alzheimer's disease paired helical filament. , 1993, The EMBO journal.

[29]  E Gratton,et al.  Quantitation of lipid phases in phospholipid vesicles by the generalized polarization of Laurdan fluorescence. , 1991, Biophysical journal.

[30]  E. Costa,et al.  Serum and depolarizing agents cause acute neurotoxicity in cultured cerebellar granule cells: role of the glutamate receptor responsive to N-methyl-D-aspartate. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[31]  C. Masters,et al.  Amyloid plaque core protein in Alzheimer disease and Down syndrome. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[32]  V. Gallo,et al.  Autoradiographic localization and depolarization-induced release of acidic amino acids in differentiating cerebellar granule cell cultures , 1984, Brain Research.

[33]  P. Calissano,et al.  In vitro cultured neurons for molecular studies correlating apoptosis with events related to Alzheimer disease , 2008, The Cerebellum.

[34]  H. Levine Quantification of beta-sheet amyloid fibril structures with thioflavin T. , 1999, Methods in enzymology.