1. Restoration of hippocampal neural precursor function by ablation of senescent cells in the aging stem cell niche.
- Author
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Fatt MP, Tran LM, Vetere G, Storer MA, Simonetta JV, Miller FD, Frankland PW, and Kaplan DR
- Subjects
- Aging, Aniline Compounds pharmacology, Animals, Cell Proliferation drug effects, Cellular Senescence drug effects, Dentate Gyrus cytology, Dentate Gyrus metabolism, Female, Hippocampus cytology, Male, Mice, Mice, Inbred C57BL, Neural Stem Cells cytology, Neurogenesis drug effects, Spatial Memory drug effects, Sulfonamides pharmacology, Cellular Senescence physiology, Neural Stem Cells metabolism, Stem Cell Niche physiology
- Abstract
Senescent cells are responsible, in part, for tissue decline during aging. Here, we focused on CNS neural precursor cells (NPCs) to ask if this is because senescent cells in stem cell niches impair precursor-mediated tissue maintenance. We demonstrate an aging-dependent accumulation of senescent cells, largely senescent NPCs, within the hippocampal stem cell niche coincident with declining adult neurogenesis. Pharmacological ablation of senescent cells via acute systemic administration of the senolytic drug ABT-263 (Navitoclax) caused a rapid increase in NPC proliferation and neurogenesis. Genetic ablation of senescent cells similarly activated hippocampal NPCs. This acute burst of neurogenesis had long-term effects in middle-aged mice. One month post-ABT-263, adult-born hippocampal neuron numbers increased and hippocampus-dependent spatial memory was enhanced. These data support a model where senescent niche cells negatively influence neighboring non-senescent NPCs during aging, and ablation of these senescent cells partially restores neurogenesis and hippocampus-dependent cognition., (Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2022
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