Expression Analysis of Zinc Transporters in Nervous Tissue Cells Reveals Neuronal and Synaptic Localization of ZIP4

Int J Mol Sci. 2021 Apr 26;22(9):4511. doi: 10.3390/ijms22094511.

Abstract

In the last years, research has shown that zinc ions play an essential role in the physiology of brain function. Zinc acts as a potent neuromodulatory agent and signaling ions, regulating healthy brain development and the function of both neurons and glial cells. Therefore, the concentration of zinc within the brain and its cells is tightly controlled. Zinc transporters are key regulators of (extra-) cellular zinc levels, and deregulation of zinc homeostasis and zinc transporters has been associated with neurodegenerative and neuropsychiatric disorders. However, to date, the presence of specific family members and their subcellular localization within brain cells have not been investigated in detail. Here, we analyzed the expression of all zinc transporters (ZnTs) and Irt-like proteins (ZIPs) in the rat brain. We further used primary rat neurons and rat astrocyte cell lines to differentiate between the expression found in neurons or astrocytes or both. We identified ZIP4 expressed in astrocytes but significantly more so in neurons, a finding that has not been reported previously. In neurons, ZIP4 is localized to synapses and found in a complex with major postsynaptic scaffold proteins of excitatory synapses. Synaptic ZIP4 reacts to short-term fluctuations in local zinc levels. We conclude that ZIP4 may have a so-far undescribed functional role at excitatory postsynapses.

Keywords: SLC30; SLC39A4; ZIP; Zinc; ZnT; brain; glia; synapse.

MeSH terms

  • Animals
  • Astrocytes / metabolism
  • Brain / metabolism
  • Carrier Proteins / metabolism*
  • Carrier Proteins / physiology
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Cell Line
  • Female
  • Gene Expression / genetics
  • Homeostasis / physiology
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue / metabolism
  • Neurons / metabolism*
  • Pregnancy
  • Primary Cell Culture
  • Rats
  • Rats, Sprague-Dawley
  • Transcriptome / genetics
  • Zinc / metabolism*

Substances

  • Carrier Proteins
  • Cation Transport Proteins
  • Slc39a4 protein, rat
  • zinc-binding protein
  • Zinc