Plasma membrane remodeling determines adipocyte expansion and mechanical adaptability

Adipocytes expand massively to accommodate excess energy stores and protect the organism from lipotoxicity. Adipose tissue expandability is at the center of disorders such as obesity and lipodystrophy; however, little is known about the relevance of adipocyte biomechanics on the etiology of these co...

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Detalles Bibliográficos
Autores: Aboy-Pardal , Maria C M, Guadamillas Mora, Marta Carmen, Guerrero , Carlos R, Catala Montoro , Mauro, Toledano-Donado , Mónica, Terrés Domínguez, Sara, Pavón , Dácil M, Jiménez Jiménez, Víctor, Jiménez Carretero, Daniel, Zamai , Moreno, Folgueira , Cintia, Cerezo , Ana, Lolo , Fidel-Nicolas, Nogueiras , Rubén, Sabio , Guadalupe, Sánchez Álvarez, Miguel, Echarri , Asier, García , Ricardo, del Pozo , Miguel A
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad de Castilla-La Mancha
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/46322
Acceso en línea:https://doi.org/10.1038/s41467-024-54224-y
https://hdl.handle.net/10578/46322
Access Level:acceso abierto
Palabra clave:Adipocytes
Caveolae
Lipid droplet
Mechanical adaptability
Obesity
Phosphoregulation
Plasma membrane
Descripción
Sumario:Adipocytes expand massively to accommodate excess energy stores and protect the organism from lipotoxicity. Adipose tissue expandability is at the center of disorders such as obesity and lipodystrophy; however, little is known about the relevance of adipocyte biomechanics on the etiology of these conditions. Here, we show in male mice in vivo that the adipocyte plasma membrane undergoes caveolar domain reorganization upon lipid droplet expansion. As the lipid droplet grows, caveolae disassemble to release their membrane reservoir and increase cell surface area, and transfer specific caveolar components to the LD surface. Adipose tissue null for caveolae is stiffer, shows compromised deformability, and is prone to rupture under mechanical compression. Mechanistically, phosphoacceptor Cav1 Tyr14 is required for caveolae disassembly: adipocytes bearing a Tyr14Phe mutation at this residue are stiffer and smaller, leading to decreased adiposity in vivo; exhibit deficient transfer of Cav1 and EHD2 to the LD surface, and show distinct Cav1 molecular dynamics and tension adaptation. These results indicate that Cav1 phosphoregulation modulates caveolar dynamics as a relevant component of the homeostatic mechanoadaptation of the differentiated adipocyte.