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A Neurite Outgrowth Assay and Neurotoxicity Assessment with Human Neural Progenitor Cell-Derived Neurons
Published on: August 6, 2020
D609-mediated inhibition of ATP synthesis in neural progenitor cells
Haviryaji S G Kalluri1, Robert J Dempsey
1aDepartment of Neurological Surgery bCardiovascular Research Center, University of Wisconsin, Madison, Wisconsin, USA.
Abstract:
Tricyclodecan-9-yl-xanthogenate (D609) is an antioxidative molecule with antiproliferative and neuroprotective properties in a variety of cells. Previously, we have shown that D609 decreased the proliferation of neural progenitor cells. In this study, we examined the antioxidative property of D609 on neural progenitor cells isolated from the subventricular zone of the rat brain. Cellular oxidation was assessed by measuring the ATP content of the cells. Our results show that D609 decreased the ATP content of the neural progenitor cells by ∼40%, suggesting the possible inhibition of cellular metabolic activity. Cytochrome c oxidase (Cox), also known as complex IV of the electron transport chain, is a terminal enzyme involved in the oxidation of substrates resulting in the generation of energy required for the cellular activity. Therefore, regulating the activity of Cox could interfere with the generation of ATP, consequently affecting the proliferation of cells. Consistent with this hypothesis, we also observed a decrease in the Cox activity following the incubation of neural progenitor cells with D609. These results suggest that D609 could inhibit the activity of Cox and subsequent ATP synthesis in the neural progenitor cells.
Insights
Tricyclodecan-9-yl-xanthogenate (D609) reduces neural progenitor cell proliferation by inhibiting ATP synthesis. This molecule decreases cellular ATP content and cytochrome c oxidase activity, impacting energy production.
Area of Science:
- Neuroscience
- Cell Biology
- Biochemistry
Background:
- Tricyclodecan-9-yl-xanthogenate (D609) exhibits antioxidative, antiproliferative, and neuroprotective effects.
- Previous studies indicated D609 reduces neural progenitor cell proliferation.
Purpose of the Study:
- To investigate the antioxidative effects of D609 on rat neural progenitor cells.
- To determine the impact of D609 on cellular ATP content and cytochrome c oxidase (Cox) activity.
Main Methods:
- Neural progenitor cells were isolated from the subventricular zone of rat brains.
- Cellular oxidation was assessed by measuring ATP content.
- Cytochrome c oxidase (Cox) activity was measured after D609 incubation.
Main Results:
- D609 decreased neural progenitor cell ATP content by approximately 40%.
- D609 incubation led to a reduction in Cox activity.
- These findings suggest D609 inhibits cellular metabolic activity and ATP synthesis.
Conclusions:
- D609 inhibits cytochrome c oxidase (Cox) activity in neural progenitor cells.
- D609 suppresses ATP synthesis, potentially explaining its antiproliferative effects.
- D609's antioxidative properties may involve the regulation of cellular energy metabolism.
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