Extracellular pH regulates autophagy via the AMPK–ULK1 pathway in rat cardiomyocytes

16Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Various pathological conditions contribute to pH fluctuations and affect the functions of vital organs such as the heart. In this study, we show that in rat cardiomyocytes, acidic extracellular pH (pHe) inhibits autophagy, whereas alkaline pHe stimulates it. We also find that adenosine monophosphate-activated protein kinase (AMPK), mammalian target of rapamycin (mTOR) and Unc-51-like kinase 1 (ULK1) are very sensitive to pHe changes. Furthermore, by interfering with AMPK, mTOR or ULK1 activity, we demonstrate that the AMPK–ULK1 pathway, but not the mTOR pathway, plays a crucial role on pHe-regulated autophagy and cardiomyocyte viability. These data provide a potential therapeutic strategy against cardiomyocyte injury triggered by pH fluctuations.

Cite

CITATION STYLE

APA

Zhao, L., Cui, L., Jiang, X., Zhang, J., Zhu, M., Jia, J., … Huang, Y. (2016). Extracellular pH regulates autophagy via the AMPK–ULK1 pathway in rat cardiomyocytes. FEBS Letters, 590(18), 3202–3212. https://doi.org/10.1002/1873-3468.12359

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free