期刊
JOURNAL OF CELLULAR PHYSIOLOGY
卷 234, 期 9, 页码 15872-15884出版社
WILEY
DOI: 10.1002/jcp.28245
关键词
cadmium; neurotoxicity; rat hippocampal neurons; Zinc; ZnT3 gene silencing
资金
- Inserm, Universite Paris Diderot, Investissement d'Avenir [ANR-11-INBS-0011]
- ERA-NET Neuron (Micromet)
- DHU PROTECT
- Association Robert Debre
- PremUP
- Fondation de France
- Fondation pour la Recherche sur le Cerveau
- Fondation des Gueules Cassees
- Roger de Spoelberch Foundation
- Grace de Monaco Foundation
- Cerebral Palsy Alliance Research Foundation Australia
- Ministry of Higher Education, Scientific Research and Technology of Tunisia
The present study examined the involvement of zinc (Zn)-transporters (ZnT3) in cadmium (Cd)-induced alterations of Zn homeostasis in rat hippocampal neurons. We treated primary rat hippocampal neurons for 24 or 48hr with various concentrations of CdCl2 (0, 0.5, 5, 10, 25, or 50M) and/or ZnCl (2) (0, 10, 30, 50, 70, or 90M), using normal neuronal medium as control. By The CellTiter 96 ((R)) Aqueous One Solution Cell Proliferation Assay (MTS; Promega, Madison, WI) assay and immunohistochemistry for cell death markers, 10 and 25M of Cd were found to be noncytotoxic doses, and both 30 and 90M of Zn as the best concentrations for cell proliferation. We tested these selected doses. Cd, at concentrations of 10 or 25M (and depending on the absence or presence of Zn), decreased the percentage of surviving cells. Cd-induced neuronal death was either apoptotic or necrotic depending on dose, as indicated by 7-AAD and/or annexin V labeling. At the molecular level, Cd exposure induced a decrease in hippocampal brain-derived neurotrophic factor-tropomyosin receptor kinase B (BDNF-TrkB) and Erk1/2 signaling, a significant downregulation of the expression of learning- and memory-related receptors and synaptic proteins such as the NMDAR NR2A subunit and PSD-95, as well as the expression of the synapse-specific vesicular Zn transporter ZnT3 in cultured hippocampal neurons. Zn supplementation, especially at the 30M concentration, led to partial or total protection against Cd neurotoxicity both with respect to the number of apoptotic cells and the expression of several genes. Interestingly, after knockdown of ZnT3 by small interfering RNA transfection, we did not find the restoration of the expression of this gene following Zn supplementation at 30M concentration. These data indicate the involvement of ZnT3 in the mechanism of Cd-induced hippocampal neurotoxicity.
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