Astrocyte-neuron metabolic cooperation shapes brain activity
Autores de IBSAL
Autores ajenos a IBSAL
- Bonvento, G
Grupos
Abstract
The brain has almost no energy reserve, but its activity coordinates organismal function, a burden that requires precise coupling between neurotransmission and energy metabolism. Deciphering how the brain accomplishes this complex task is crucial to understand central facets of human physiology and disease mechanisms. Each type of neural cell displays a peculiar metabolic signature, forcing the intercellular exchange of metabolites that serve as both energy precursors and paracrine signals. The paradigm of this biological feature is the astrocyte-neuron couple, in which the glycolytic metabolism of astrocytes contrasts with the mitochondrial oxidative activity of neurons. Astrocytes generate abundant mitochondrial reactive oxygen species and shuttle to neurons glycolytically derived metabolites, such as L-lactate and L-serine, which sustain energy needs, conserve redox status, and modulate neurotransmitter-receptor activity. Conversely, early disruption of this metabolic cooperation may contribute to the initiation or progression of several neurological diseases, thus requiring innovative therapies to preserve brain energetics.
Datos de la publicación
- ISSN/ISSNe:
- 1550-4131, 1932-7420
- Tipo:
- Review
- Páginas:
- 1546-1564
Cell Metabolism CELL PRESS
Citas Recibidas en Web of Science: 177
Documentos
- No hay documentos
Filiaciones
Financiación
Proyectos asociados
3. Frailty and Aging. 3.1. Healthy aging biological mechanisms oriented to the maintenance of functional autonomy and mechanisms leading to frailty and disability. CICERFES
Investigador Principal: Juan Pedro Bolaños Hernández
CB16/10/00282 . Instituto de Salud Carlos III . 2017
Cita
Bonvento G,Bolanos JP. Astrocyte-neuron metabolic cooperation shapes brain activity. Cell Metab. 2021. 33(8):p. 1546-1564. IF:31,373. (1).
Bonvento G, Bolanos JP. Astrocyte-neuron metabolic cooperation shapes brain activity, Cell Metabolism. 2021; 33(8): p. 1546-1564. FI: 31,373(Q1) (D1)