Role of zinc transporter ZIP12 in susceptibility-weighted brain magnetic resonance imaging (MRI) phenotypes and mitochondrial function

FASEB J. 2020 Sep;34(9):10702-12725. doi: 10.1096/fj.202000772R. Epub 2020 Jul 27.

Abstract

Brain zinc dysregulation is linked to many neurological disorders. However, the mechanisms regulating brain zinc homeostasis are poorly understood. We performed secondary analyses of brain MRI GWAS and exome sequencing data from adults in the UK Biobank. Coding ZIP12 polymorphisms in zinc transporter ZIP12 (SLC39A12) were associated with altered brain susceptibility weighted MRI (swMRI). Conditional and joint association analyses revealed independent GWAS signals in linkage disequilibrium with 2 missense ZIP12 polymorphisms, rs10764176 and rs72778328, with reduced zinc transport activity. ZIP12 rare coding variants predicted to be deleterious were associated with similar impacts on brain swMRI. In Neuro-2a cells, ZIP12 deficiency by short hairpin RNA (shRNA) depletion or CRISPR/Cas9 genome editing resulted in impaired mitochondrial function, increased superoxide presence, and detectable protein carbonylation. Inhibition of Complexes I and IV of the electron transport chain reduced neurite outgrowth in ZIP12 deficient cells. Transcriptional coactivator PGC-1α, mitochondrial superoxide dismutase (SOD2), and chemical antioxidants α-tocopherol, MitoTEMPO, and MitoQ restored neurite extension impaired by ZIP12 deficiency. Mutant forms of α-synuclein and tau linked to familial Parkinson's disease and frontotemporal dementia, respectively, reduced neurite outgrowth in cells deficient in ZIP12. Zinc and ZIP12 may confer resilience against neurological diseases or premature aging of the brain.

Keywords: SLC39A12; metal homeostasis; mitochondria; neurite outgrowth; neurodegeneration; nutrigenomics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Brain / diagnostic imaging
  • Brain / metabolism*
  • CHO Cells
  • Cation Transport Proteins / deficiency
  • Cation Transport Proteins / genetics*
  • Cation Transport Proteins / metabolism
  • Cell Line, Tumor
  • Cricetinae
  • Cricetulus
  • Humans
  • Magnetic Resonance Imaging / methods*
  • Mice
  • Mitochondria / genetics*
  • Mitochondria / metabolism
  • Neuronal Outgrowth / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism
  • Polymorphism, Single Nucleotide
  • RNA Interference
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Zinc / metabolism

Substances

  • Cation Transport Proteins
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • SLC39A12 protein, human
  • Superoxide Dismutase
  • superoxide dismutase 2
  • Zinc