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Evidence That the ZNT3 Protein Controls the Total Amount of Elemental Zinc in Synaptic Vesicles
Author(s) -
David H. Linkous,
Jane M. Flinn,
Jae Young Koh,
Antonio Lanzirotti,
Paul M. Bertsch,
Blair F. Jones,
Leonard J. Giblin,
Christopher J. Frederickson
Publication year - 2007
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1369/jhc.6a7035.2007
Subject(s) - zinc , synaptic vesicle , chemistry , vesicle , mossy fiber (hippocampus) , hippocampal formation , microprobe , biophysics , microbiology and biotechnology , biochemistry , biology , neuroscience , mineralogy , dentate gyrus , organic chemistry , membrane
The ZNT3 protein decorates the presynaptic vesicles of central neurons harboring vesicular zinc, and deletion of this protein removes staining for zinc. However, it has been unclear whether only histochemically reactive zinc is lacking or if, indeed, total elemental zinc is missing from neurons lacking the Slc30a3 gene, which encodes the ZNT3 protein. The limitations of conventional histochemical procedures have contributed to this enigma. However, a novel technique, microprobe synchrotron X-ray fluorescence, reveals that the normal 2- to 3-fold elevation of zinc concentration normally present in the hippocampal mossy fibers is absent in Slc30a3 knockout (ZNT3) mice. Thus, the ZNT3 protein evidently controls not only the "stainability" but also the actual mass of zinc in mossy-fiber synaptic vesicles. This work thus confirms the metal-transporting role of the ZNT3 protein in the brain.

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