Authors
Gabriella M. Forte
Elizabeth Davie
Shervi Lie
Mirita Franz-Wachtel
Ashley J. Ovens, Australian Catholic UniversityFollow
Tingting Wang
Jonathan S. Oakhill, Australian Catholic UniversityFollow
Boris Maček
Iain M. Hagan
Janni Petersen
Publication Date
2019
Publication Details
Forte, G. M, Davie, E., Lie, S., Franz-Wachtel, M., Ovens, A. J, Wang, T., Oakhill, J. S, Maček, B., Hagan, I. M & Petersen, J. (2019). Import of extracellular ATP in yeast and man modulates AMPK and TORC1 signalling. Journal of Cell Science,132(7), 1-15. United Kingdom: The Company of Biologists Ltd.. Retrieved from https://doi.org/10.1242/jcs.223925
Abstract
AMP-activated kinase (AMPK) and target of rapamycin (TOR) signalling coordinate cell growth, proliferation, metabolism and cell survival with the nutrient environment of cells. The poor vasculature and nutritional stress experienced by cells in solid tumours raises the question: how do they assimilate sufficient nutrients to survive? Here, we show that human and fission yeast cells import ATP and AMP from their external environment to regulate AMPK and TOR signalling. Exposure of fission yeast (Schizosaccharomyces pombe) and human cells to external AMP impeded cell growth; however, in yeast this restraining impact required AMPK. In contrast, external ATP rescued the growth defect of yeast mutants with reduced TORC1 signalling; furthermore, exogenous ATP transiently enhanced TORC1 signalling in both yeast and human cell lines. Addition of the PANX1 channel inhibitor probenecid blocked ATP import into human cell lines suggesting that this channel may be responsible for both ATP release and uptake in mammals. In light of these findings, it is possible that the higher extracellular ATP concentration reported in solid tumours is both scavenged and recognized as an additional energy source beneficial for cell growth.
School/Institute
Mary MacKillop Institute for Health Research
Document Type
Open Access Journal Article
Access Rights
Open Access
Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 License.