Cargando…

Fatty acid oxidation organizes mitochondrial supercomplexes to sustain astrocytic ROS and cognition

Having direct access to brain vasculature, astrocytes can take up available blood nutrients and metabolize them to fulfil their own energy needs and deliver metabolic intermediates to local synapses(1,2). These glial cells should be, therefore, metabolically adaptable to swap different substrates. H...

Descripción completa

Detalles Bibliográficos
Autores principales: Morant-Ferrando, Brenda, Jimenez-Blasco, Daniel, Alonso-Batan, Paula, Agulla, Jesús, Lapresa, Rebeca, Garcia-Rodriguez, Dario, Yunta-Sanchez, Sara, Lopez-Fabuel, Irene, Fernandez, Emilio, Carmeliet, Peter, Almeida, Angeles, Garcia-Macia, Marina, Bolaños, Juan P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447235/
https://www.ncbi.nlm.nih.gov/pubmed/37460843
http://dx.doi.org/10.1038/s42255-023-00835-6
Descripción
Sumario:Having direct access to brain vasculature, astrocytes can take up available blood nutrients and metabolize them to fulfil their own energy needs and deliver metabolic intermediates to local synapses(1,2). These glial cells should be, therefore, metabolically adaptable to swap different substrates. However, in vitro and in vivo studies consistently show that astrocytes are primarily glycolytic(3–7), suggesting glucose is their main metabolic precursor. Notably, transcriptomic data(8,9) and in vitro(10) studies reveal that mouse astrocytes are capable of mitochondrially oxidizing fatty acids and that they can detoxify excess neuronal-derived fatty acids in disease models(11,12). Still, the factual metabolic advantage of fatty acid use by astrocytes and its physiological impact on higher-order cerebral functions remain unknown. Here, we show that knockout of carnitine-palmitoyl transferase-1A (CPT1A)—a key enzyme of mitochondrial fatty acid oxidation—in adult mouse astrocytes causes cognitive impairment. Mechanistically, decreased fatty acid oxidation rewired astrocytic pyruvate metabolism to facilitate electron flux through a super-assembled mitochondrial respiratory chain, resulting in attenuation of reactive oxygen species formation. Thus, astrocytes naturally metabolize fatty acids to preserve the mitochondrial respiratory chain in an energetically inefficient disassembled conformation that secures signalling reactive oxygen species and sustains cognitive performance.