Title | Soluble adenylyl cyclase is essential for proper lysosomal acidification. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Rahman N, Ramos-Espiritu L, Milner TA, Buck J, Levin LR |
Journal | J Gen Physiol |
Volume | 148 |
Issue | 4 |
Pagination | 325-39 |
Date Published | 2016 Oct |
ISSN | 1540-7748 |
Keywords | Adenylyl Cyclases, Animals, Brain, Cell Line, Fibroblasts, Gene Expression Regulation, Enzymologic, Lysosomes, Mice, Mice, Knockout, Purines |
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. |
DOI | 10.1085/jgp.201611606 |
Alternate Journal | J. Gen. Physiol. |
PubMed ID | 27670898 |
PubMed Central ID | PMC5037342 |
Grant List | F31 NS081930 / NS / NINDS NIH HHS / United States R01 GM062328 / GM / NIGMS NIH HHS / United States R01 GM107442 / GM / NIGMS NIH HHS / United States R01 NS055255 / NS / NINDS NIH HHS / United States |