No energy, no autophagy—Mechanisms and therapeutic implications of autophagic response energy requirements

Author:

Mandic Milos1ORCID,Paunovic Verica1ORCID,Vucicevic Ljubica2ORCID,Kosic Milica1ORCID,Mijatovic Srdjan3ORCID,Trajkovic Vladimir1ORCID,Harhaji‐Trajkovic Ljubica2ORCID

Affiliation:

1. Institute of Microbiology and Immunology, Faculty of Medicine University of Belgrade Belgrade Serbia

2. Department of Neurophysiology, Institute for Biological Research “Sinisa Stankovic”, National Institute of Republic of Serbia University of Belgrade Belgrade Serbia

3. Clinic for Emergency Surgery University Clinical Centre of Serbia Belgrade Serbia

Abstract

AbstractAutophagy is a lysosome‐mediated self‐degradation process of central importance for cellular quality control. It also provides macromolecule building blocks and substrates for energy metabolism during nutrient or energy deficiency, which are the main stimuli for autophagy induction. However, like most biological processes, autophagy itself requires ATP, and there is an energy threshold for its initiation and execution. We here present the first comprehensive review of this often‐overlooked aspect of autophagy research. The studies in which ATP deficiency suppressed autophagy in vitro and in vivo were classified according to the energy pathway involved (oxidative phosphorylation or glycolysis). A mechanistic insight was provided by pinpointing the critical ATP‐consuming autophagic events, including transcription/translation/interaction of autophagy‐related molecules, autophagosome formation/elongation, autophagosome fusion with the lysosome, and lysosome acidification. The significance of energy‐dependent fine‐tuning of autophagic response for preserving the cell homeostasis, and potential implications for the therapy of cancer, autoimmunity, metabolic disorders, and neurodegeneration are discussed.

Publisher

Wiley

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