Soluble adenylyl cyclase is essential for proper lysosomal acidification

Author:

Rahman Nawreen12,Ramos-Espiritu Lavoisier1,Milner Teresa A.34,Buck Jochen1,Levin Lonny R.1

Affiliation:

1. Department of Pharmacology, Weill Cornell Medical College, New York, NY 10065

2. Graduate Program in Neuroscience, Weill Cornell Medical College, New York, NY 10065

3. Feil Family Brain and Mind Research Institute, Weill Cornell Medical College, New York, NY 10065

4. Laboratory of Neuroendocrinology, The Rockefeller University, New York, NY 10065

Abstract

Lysosomes, the degradative organelles of the endocytic and autophagic pathways, function at an acidic pH. Lysosomes are acidified by the proton-pumping vacuolar ATPase (V-ATPase), but the molecular processes that set the organelle’s pH are not completely understood. In particular, pH-sensitive signaling enzymes that can regulate lysosomal acidification in steady-state physiological conditions have yet to be identified. Soluble adenylyl cyclase (sAC) is a widely expressed source of cAMP that serves as a physiological pH sensor in cells. For example, in proton-secreting epithelial cells, sAC is responsible for pH-dependent translocation of V-ATPase to the luminal surface. Here we show genetically and pharmacologically that sAC is also essential for lysosomal acidification. In the absence of sAC, V-ATPase does not properly localize to lysosomes, lysosomes fail to fully acidify, lysosomal degradative capacity is diminished, and autophagolysosomes accumulate.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Physiology

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