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Zinc homeostatic proteins in the CNS are regulated by crosstalk between extracellular and intracellular zinc

✍ Scribed by Natalya Karol; Claude Brodski; Yuval Bibi; Tehila Kaisman; Michal Forberg; Michal Hershfinkel; Israel Sekler; William F. Silverman


Book ID
102314059
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
426 KB
Volume
224
Category
Article
ISSN
0021-9541

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✦ Synopsis


Abstract

Release of Zn^2+^ from presynaptic glutamatergic terminals has long been considered the principle challenge necessitating the existence of zinc homeostatic proteins (ZHP) in the mammalian nervous system. It is now known that neural cells also possess an intracellular zinc pool, termed here [Zn^2+^]~i~, which functions in a cell signaling context. A major challenge is characterizing the interaction of these two populations of zinc ions. To assess the relationship of this Zn^2+^ pool to cellular ZHP production, we employed immunofluorescence and immunoblot analysis to compare the expression of ZHP's ZnT‐1 and MT‐I/II in olfactory bulb and hippocampus of wild‐type and ZnT‐3 KO mice, which lack synaptic Zn^2+^. In both areas, the respective distribution and concentration of ZnT‐1 and MT‐I/II were identical in ZnT‐3 KO and control animals. We subsequently examined ZHP content in ZnT‐3 KO and WT mice treated with a membrane‐permeable Zn^2+^ chelator. In both olfactory bulb and hippocampus of the KO mice, the ZHP content was significantly reduced 15 h after chelation of [Zn^2+^]~i~ compared to WT controls. Our findings support the conclusion that ZHP expression is regulated by crosstalk between synaptic and intracellular pools of Zn^2+^. J. Cell. Physiol. 224: 567–574, 2010. © 2010 Wiley‐Liss, Inc.