| Literature DB >> 26299452 |
Francesc Baixauli1, Rebeca Acín-Pérez2, Carolina Villarroya-Beltrí1, Carla Mazzeo3, Norman Nuñez-Andrade1, Enrique Gabandé-Rodriguez4, Maria Dolores Ledesma4, Alberto Blázquez5, Miguel Angel Martin5, Juan Manuel Falcón-Pérez6, Juan Miguel Redondo7, Jose Antonio Enríquez2, Maria Mittelbrunn8.
Abstract
The endolysosomal system is critical for the maintenance of cellular homeostasis. However, how endolysosomal compartment is regulated by mitochondrial function is largely unknown. We have generated a mouse model with defective mitochondrial function in CD4(+) T lymphocytes by genetic deletion of the mitochondrial transcription factor A (Tfam). Mitochondrial respiration deficiency impairs lysosome function, promotes p62 and sphingomyelin accumulation, and disrupts endolysosomal trafficking pathways and autophagy, thus linking a primary mitochondrial dysfunction to a lysosomal storage disorder. The impaired lysosome function in Tfam-deficient cells subverts T cell differentiation toward proinflammatory subsets and exacerbates the in vivo inflammatory response. Restoration of NAD(+) levels improves lysosome function and corrects the inflammatory defects in Tfam-deficient T cells. Our results uncover a mechanism by which mitochondria regulate lysosome function to preserve T cell differentiation and effector functions, and identify strategies for intervention in mitochondrial-related diseases.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26299452 PMCID: PMC5026297 DOI: 10.1016/j.cmet.2015.07.020
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287