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Updated: Jan 26, 2026

Organotypic Cultures of Adult Human Cortex as an Ex vivo Model for Human Stem Cell Transplantation and Validation
Published on: December 9, 2022
Oxidative Stress-Tolerant Stem Cells from Human Exfoliated Deciduous Teeth Decrease Hydrogen Peroxide-Induced Damage
Li Xiao1, Chikako Saiki2, Hisashi Okamura3
1Department of Pharmacology, School of Life Dentistry at Tokyo, The Nippon Dental University, 1-9-20 Fujimi, Chiyoda-ku, Tokyo 102-0071, Japan. xiaoli@tky.ndu.ac.jp.
Oxidative stress-tolerant stem cells from deciduous teeth (OST-SHED) show superior neuroprotection against oxidative brain damage compared to normal stem cells. These findings highlight OST-SHED as a promising therapeutic for brain injuries and neurodegenerative diseases.
Area of Science:
- Neuroscience
- Stem Cell Biology
- Regenerative Medicine
Background:
- Oxidative stress is a key factor in central nervous system injuries like ischemic brain damage (IBD), traumatic brain injury (TBI), and neurodegenerative disorders.
- Organotypic brain slice cultures (OBSCs) provide a model to study neuroprotection.
Purpose of the Study:
- To investigate the neuroprotective effects of stem cells from human exfoliated deciduous teeth (SHED) against oxidative stress in OBSCs.
- To compare the efficacy of normal SHED and oxidative stress-tolerant SHED (OST-SHED).
Main Methods:
- Induction of oxidative stress using hydrogen peroxide (H₂O₂) in OBSCs.
- Co-cultivation of OBSCs with normal SHED and OST-SHED.
- Assessment of cell viability (Presto Blue assay), neuronal survival, progenitor proliferation, and DNA damage (ELISA).
- Immunostaining to evaluate neuronal differentiation and marker expression.
Main Results:
- Both normal SHED and OST-SHED protected against H₂O₂-induced cell death and increased mature neurons and progenitors in OBSCs.
- OST-SHED, but not normal SHED, exhibited neuronal morphology and expressed neuronal markers during co-cultivation.
- Both SHED types reduced oxidative DNA damage; OST-SHED demonstrated superior neuroprotection despite lower viability.
- SHED produced brain-derived neurotrophic factor (BDNF) and promoted IL-6 production.
Conclusions:
- SHED, particularly OST-SHED, can prevent oxidative stress-induced brain damage.
- OST-SHED shows significant therapeutic potential for conditions like IBD, TBI, and neurodegenerative disorders.
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