AMPK activation promotes lipid droplet dispersion on detyrosinated microtubules to increase mitochondrial fatty acid oxidation

Lipid droplets (LDs) are intracellular organelles that provide fatty acids (FAs) to cellular processes including synthesis of membranes and production of metabolic energy. While known to move bidirectionally along microtubules (MTs), the role of LD motion and whether it facilitates interaction with...

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Detalles Bibliográficos
Autores: Herms Fiol, Albert, Bosch i Rodríguez, Marta, Reddy, Babu J. N., Schieber, Nicole L., Fajardo, Alba, Rupérez, Celia, Fernández-Vidal, Andrea, Rentero Alfonso, Carles, Tebar Ramon, Francesc, Enrich Bastús, Carles, Parton, Robert G., Gross, Steven P., Pol i Sorolla, Albert
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/118508
Acceso en línea:https://hdl.handle.net/2445/118508
Access Level:acceso abierto
Palabra clave:Metabolisme dels lípids
Transport biològic
Mitocondris
Microtúbuls
Lipid metabolism
Biological transport
Mitochondria
Microtubules
Descripción
Sumario:Lipid droplets (LDs) are intracellular organelles that provide fatty acids (FAs) to cellular processes including synthesis of membranes and production of metabolic energy. While known to move bidirectionally along microtubules (MTs), the role of LD motion and whether it facilitates interaction with other organelles are unclear. Here we show that during nutrient starvation, LDs and mitochondria relocate on detyrosinated MT from the cell centre to adopt a dispersed distribution. In the cell periphery, LD-mitochondria interactions increase and LDs efficiently supply FAs for mitochondrial beta-oxidation. This cellular adaptation requires the activation of the energy sensor AMPK, which in response to starvation simultaneously increases LD motion, reorganizes the network of detyrosinated MTs and activates mitochondria. In conclusion, we describe the existence of a specialized cellular network connecting the cellular energetic status and MT dynamics to coordinate the functioning of LDs and mitochondria during nutrient scarcity.