Abstract
Adult neurogenesis initiated by neural stem cells (NSCs) contributes to brain homeostasis, damage repair, and cognition. Energy metabolism plays a pivotal role in neurogenic cell fate decisions regarding self-renewal, expansion and multilineage differentiation. NSCs need to fine-tune quiescence and proliferation/commitment to guarantee lifelong neurogenesis and avoid premature exhaustion. Accumulating evidence supports a model whereby calorie restriction or increased energy expenditure reinforce NSC quiescence and promote self-renewal. Conversely, growth/proliferation inputs and anabolic signals, although necessary for neurogenesis, deplete the NSCs pool in the long run. This framework incorporates the emerging neurogenic roles of nutrient-sensing signaling pathways, providing a rationale for the alarming connection between nutritional imbalances, metabolic disorders and accelerated brain aging.
Lingua originale | English |
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pagine (da-a) | 756-769 |
Numero di pagine | 14 |
Rivista | Trends in Endocrinology and Metabolism |
Volume | 27 |
DOI | |
Stato di pubblicazione | Pubblicato - 2016 |
Keywords
- adult neurogenesis
- brain aging
- metabolism
- neural stem cells (NSC)
- self-renewal