[HTML][HTML] Cell-autonomous death of cerebellar purkinje neurons with autophagy in Niemann-Pick type C disease

DC Ko, L Milenkovic, SM Beier, H Manuel… - PLoS …, 2005 - journals.plos.org
DC Ko, L Milenkovic, SM Beier, H Manuel, JA Buchanan, MP Scott
PLoS genetics, 2005journals.plos.org
Niemann-Pick type C is a neurodegenerative lysosomal storage disorder caused by
mutations in either of two genes, npc1 and npc2. Cells lacking Npc1, which is a
transmembrane protein related to the Hedgehog receptor Patched, or Npc2, which is a
secreted cholesterol-binding protein, have aberrant organelle trafficking and accumulate
large quantities of cholesterol and other lipids. Though the Npc proteins are produced by all
cells, cerebellar Purkinje neurons are especially sensitive to loss of Npc function. Since …
Niemann-Pick type C is a neurodegenerative lysosomal storage disorder caused by mutations in either of two genes, npc1 and npc2. Cells lacking Npc1, which is a transmembrane protein related to the Hedgehog receptor Patched, or Npc2, which is a secreted cholesterol-binding protein, have aberrant organelle trafficking and accumulate large quantities of cholesterol and other lipids. Though the Npc proteins are produced by all cells, cerebellar Purkinje neurons are especially sensitive to loss of Npc function. Since Niemann-Pick type C disease involves circulating molecules such as sterols and steroids and a robust inflammatory response within the brain parenchyma, it is crucial to determine whether external factors affect the survival of Purkinje cells (PCs). We investigated the basis of neurodegeneration in chimeric mice that have functional npc1 in only some cells. Death of mutant npc1 cells was not prevented by neighboring wild-type cells, and wild-type PCs were not poisoned by surrounding mutant npc1 cells. PCs undergoing cell-autonomous degeneration have features consistent with autophagic cell death. Chimeric mice exhibited a remarkable delay and reduction of wasting and ataxia despite their substantial amount of mutant tissue and dying cells, revealing a robust mechanism that partially compensates for massive PC death.
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