Mitochondria supply ATP to the ER through a mechanism antagonized by cytosolic Ca2+

• DOI: 10.7554/elife.49682
• Publication Date: 2019-09-09T12:00:22Z
• Authors: Jing Yong; Helmut Bischof; Sandra Burgstaller; Marina Siirin; Anne Murphy; Roland Malli; Randal J Kaufman
• Keywords: 0301 basic medicine; organelle bioenergetics; QH301-705.5; Cations, Divalent; Science; Endoplasmic Reticulum; Cell Line; 03 medical and health sciences; Adenosine Triphosphate; Cricetulus; Biochemistry and Chemical Biology; protein folding; Chinese hamster ovary cell; Animals; Humans; SLC35B1/AXER protein; Biology (General); Q; R; Biological Transport; Mitochondria; Rats; Medicine; Calcium; ATP and adenosine nucleotides transport; ER stress

The endoplasmic reticulum (ER) imports ATP and uses energy from ATP hydrolysis for protein folding and trafficking. However, little is known about how this vital ATP transport occurs across the ER membrane. Here, using three commonly used cell lines (CHO, INS1 and HeLa), we report that ATP enters the ER lumen through a cytosolic Ca2+-antagonized mechanism, or CaATiER (Ca2+-Antagonized Transport into ER). Significantly, we show that mitochondria supply ATP to the ER and a SERCA-dependent Ca2+ gradient across the ER membrane is necessary for ATP transport into the ER, through SLC35B1/AXER. We propose that under physiological conditions, increases in cytosolic Ca2+ inhibit ATP import into the ER lumen to limit ER ATP consumption. Furthermore, the ATP level in the ER is readily depleted by oxidative phosphorylation (OxPhos) inhibitors and that ER protein misfolding increases ATP uptake from mitochondria into the ER. These findings suggest that ATP usage in the ER may increase mitochondrial OxPhos while decreasing glycolysis, i.e. an ‘anti-Warburg’ effect.