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Published on: March 31, 2015
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Vesicular Zinc Modulates Cell Proliferation and Survival in the Developing Hippocampus
Selena Fu1,2,3, Ashley T Cho1, Simon C Spanswick1,2
1Hotchkiss Brain Institute, University of Calgary, Calgary, AB T2N 1N4, Canada.
Cells
|March 29, 2023
Summary
Loss of vesicular zinc impacts early brain development, affecting cell proliferation and survival differently in male and female mice across postnatal ages. This research highlights crucial sex- and age-dependent variations in neurogenesis.
Area of Science:
- Neuroscience
- Developmental Biology
- Cell Biology
Background:
- Vesicular zinc, stored in synaptic vesicles by zinc transporter 3 (ZnT3), influences neuronal signaling.
- Research on vesicular zinc has primarily focused on adult neurogenesis in the hippocampus.
- Its role in early postnatal neurogenesis remains less understood.
Purpose of the Study:
- To investigate the role of vesicular zinc in modulating neurogenesis during early postnatal development.
- To evaluate cell proliferation, survival, and neuronal differentiation in ZnT3 knockout mice.
- To identify potential sex- and age-dependent differences in neurogenesis.
Main Methods:
- Utilized ZnT3 knockout (KO) mice lacking vesicular zinc.
- Assessed cell proliferation at postnatal days P6, P14, and P28.
- Evaluated cell survival and neuronal phenotype in adulthood using BrdU labeling.
Main Results:
- ZnT3 KO mice showed reduced cell proliferation at P14 but increased survival to adulthood.
- Cells labeled at P6 exhibited enhanced survival to adulthood in both male and female KO mice.
- Observed sex-dependent differences in proliferation, survival, and neuronal differentiation, with age-dependent effects of BrdU injection timing.
Conclusions:
- Loss of vesicular zinc significantly alters postnatal neurogenesis, affecting cell proliferation and survival.
- Results reveal prominent sex- and age-dependent variations in developmental neurogenesis.
- This study provides a foundation for further research into vesicular zinc's role in neurogenesis modulation.

