Prion Pathogenesis is Independent of Caspase-12

Andrew D. Steele, Claudio Hetz, Caroline H. Yi, Walker S. Jackson, Andrew W. Borkowski, Junying Yuan, Robert H. Wollmann and Susan Lindquist

volume 1 | issue 4

october/november/december 2007
Pages: 243 - 247

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The pathogenic mechanism(s) underlying neurodegenerative diseases associated with protein misfolding is unclear. Several studies have implicated ER stress pathways in neurodegenerative conditions, including prion disease, amyotrophic lateral sclerosis, Alzheimer's disease and many others. The ER stress response and up-regulation of ER stress-responsive chaperones is observed in the brains of patients affected with Creutzfeldt-Jacob disease and in mouse models of prion diseases. In particular, the processing of caspase-12, an ER-localized caspase, correlates with neuronal cell death in prion disease. However, the contribution of caspase-12 to neurodegeneration has not been directly addressed in vivo. We confirm that ER stress is induced and that caspase-12 is proteolytically processed in a murine model of infectious prion disease. To address the causality of caspase-12 in mediating infectious prion pathogenesis, we inoculated mice deficient in caspase-12 with prions. The survival, behavior, pathology and accumulation of proteinase K-resistant PrP are indistinguishable between caspase-12 knockout and control mice, suggesting that caspase-12 is not necessary for mediating the neurotoxic effects of prion protein misfolding.

Authors

Andrew D. Steele

Whitehead Insititute, Massachusetts Institute of Technology

Claudio Hetz

Institute of Biomedical Sciences, University of Chile

Caroline H. Yi

Harvard Medical School

Walker S. Jackson

Whitehead Institute for Biomedical Research, Howard Hughes Medical Institute

Andrew W. Borkowski