1. Academic Validation
  2. Chaperone-mediated autophagy protects against hyperglycemic stress

Chaperone-mediated autophagy protects against hyperglycemic stress

  • Autophagy. 2023 Oct 5. doi: 10.1080/15548627.2023.2267415.
Emilio J Vélez 1 Simon Schnebert 1 Maxime Goguet 1 Sara Balbuena-Pecino 1 Karine Dias 1 Linda Beauclair 1 Stéphanie Fontagné-Dicharry 1 Vincent Véron 1 Alexandra Depincé 2 Florian Beaumatin 1 Amaury Herpin 2 Iban Seiliez 1
Affiliations

Affiliations

  • 1 Université de Pau et des Pays de l'Adour, Saint-Pée-sur-Nivelle, France.
  • 2 INRAE, UR1037 Laboratory of Fish Physiology and Genomics, Rennes, France.
Abstract

Chaperone-mediated Autophagy (CMA) is a major pathway of lysosomal proteolysis critical for cellular homeostasis and metabolism, and whose defects have been associated with several human pathologies. While CMA has been well described in mammals, functional evidence has only recently been documented in fish, opening up new perspectives to tackle this function under a novel angle. Now we propose to explore CMA functions in the rainbow trout (RT, Oncorhynchus mykiss), a fish species recognized as a model organism of glucose intolerance and characterized by the presence of two paralogs of the CMA-limiting factor Lamp2A (lysosomal associated membrane protein 2A). To this end, we validated a fluorescent reporter (KFERQ-PA-mCherry1) previously used to track functional CMA in mammalian cells, in an RT hepatoma-derived cell line (RTH-149). We found that incubation of cells with high-glucose levels (HG, 25 mM) induced translocation of the CMA reporter to lysosomes and/or late endosomes in a KFERQ- and Lamp2A-dependent manner, as well as reduced its half-life compared to the control (5 mM), thus demonstrating increased CMA flux. Furthermore, we observed that activation of CMA upon HG exposure was mediated by generation of mitochondrial Reactive Oxygen Species, and involving the antioxidant transcription factor Nfe2l2/Nrf2 (nfe2 like bZIP transcription factor 2). Finally, we demonstrated that CMA plays an important protective role against HG-induced stress, primarily mediated by one of the two RT Lamp2As. Together, our results provide unequivocal evidence for CMA activity existence in RT and highlight both the role and regulation of CMA during glucose-related metabolic disorders.

Keywords

CMA; Lamp2A; NFE2L2/NRF2; ROS; RTH-149; fish; glucose; glucose intolerance; metabolism; trout.

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