Altered transition metal homeostasis in Niemann-Pick disease, type C1

Metallomics. 2014 Mar;6(3):542-53. doi: 10.1039/c3mt00308f. Epub 2013 Dec 16.

Abstract

The loss of NPC1 protein function is the predominant cause of Niemann-Pick type C1 disease (NP-C1), a systemic and neurodegenerative disorder characterized by late-endosomal/lysosomal accumulation of cholesterol and other lipids. Limited evidence from post-mortem human tissues, an Npc1(-/-) mouse model, and cell culture studies also suggest failure of metal homeostasis in NP-C1. To investigate these findings, we performed a comprehensive transition metal analysis of cerebrospinal fluid (CSF), plasma and tissue samples from human NP-C1 patients and an Npc1(-/-) mouse model. NPC1 deficiency in the Npc1(-/-) mouse model resulted in a perturbation of transition metal homeostasis in the plasma and key organs (brain, liver, spleen, heart, lungs, and kidneys). Analysis of human patient CSF, plasma and post-mortem brain tissues also indicated disrupted metal homeostasis. There was a disparity in the direction of metal changes between the human and the Npc1(-/-) mouse samples, which may reflect species-specific metal metabolism. Nevertheless, common to both species is brain zinc accumulation. Furthermore, treatment with the glucosylceramide synthase inhibitor miglustat, the only drug shown in a controlled clinical trial to have some efficacy for NP-C1, did not correct the alterations in CSF and plasma transition metal and ceruloplasmin (CP) metabolism in NP-C1 patients. These findings highlight the importance of NPC1 function in metal homeostasis, and indicate that metal-targeting therapy may be of value as a treatment for NP-C.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Deoxynojirimycin / analogs & derivatives
  • 1-Deoxynojirimycin / therapeutic use
  • Animals
  • Brain / metabolism
  • Brain / pathology
  • Ceruloplasmin / antagonists & inhibitors
  • Ceruloplasmin / metabolism
  • Enzyme Inhibitors / therapeutic use
  • Female
  • Gene Deletion
  • Homeostasis
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Metals / blood
  • Metals / cerebrospinal fluid
  • Metals / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Niemann-Pick C1 Protein
  • Niemann-Pick Disease, Type C / blood
  • Niemann-Pick Disease, Type C / cerebrospinal fluid
  • Niemann-Pick Disease, Type C / drug therapy
  • Niemann-Pick Disease, Type C / metabolism*
  • Proteins / genetics
  • Transition Elements / blood
  • Transition Elements / cerebrospinal fluid
  • Transition Elements / metabolism*

Substances

  • Enzyme Inhibitors
  • Intracellular Signaling Peptides and Proteins
  • Metals
  • Niemann-Pick C1 Protein
  • Npc1 protein, mouse
  • Proteins
  • Transition Elements
  • 1-Deoxynojirimycin
  • miglustat
  • Ceruloplasmin