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Title: RNA SEQ Analysis Indicates that the AE3 Cl-/HCO3- Exchanger Contributes to Active Transport-Mediated CO2 Disposal in Heart.

Authors: Vairamani, Kanimozhi; Wang, Hong-Sheng; Medvedovic, Mario; Lorenz, John N; Shull, Gary E

Published In Sci Rep, (2017 Aug 04)

Abstract: Loss of the AE3 Cl-/HCO3- exchanger (Slc4a3) in mice causes an impaired cardiac force-frequency response and heart failure under some conditions but the mechanisms are not known. To better understand the functions of AE3, we performed RNA Seq analysis of AE3-null and wild-type mouse hearts and evaluated the data with respect to three hypotheses (CO2 disposal, facilitation of Na+-loading, and recovery from an alkaline load) that have been proposed for its physiological functions. Gene Ontology and PubMatrix analyses of differentially expressed genes revealed a hypoxia response and changes in vasodilation and angiogenesis genes that strongly support the CO2 disposal hypothesis. Differential expression of energy metabolism genes, which indicated increased glucose utilization and decreased fatty acid utilization, were consistent with adaptive responses to perturbations of O2/CO2 balance in AE3-null myocytes. Given that the myocardium is an obligate aerobic tissue and consumes large amounts of O2, the data suggest that loss of AE3, which has the potential to extrude CO2 in the form of HCO3-, impairs O2/CO2 balance in cardiac myocytes. These results support a model in which the AE3 Cl-/HCO3- exchanger, coupled with parallel Cl- and H+-extrusion mechanisms and extracellular carbonic anhydrase, is responsible for active transport-mediated disposal of CO2.

PubMed ID: 28779178 Exiting the NIEHS site

MeSH Terms: Adenosine Triphosphate/metabolism; Animals; Antiporters/genetics*; Antiporters/metabolism*; Biological Transport, Active; Carbon Dioxide/metabolism*; Computational Biology/methods; Energy Metabolism/genetics; Fatty Acids/metabolism; Gene Expression; Gene Ontology; Glucose/metabolism; Hydrogen-Ion Concentration; Hypoxia/metabolism; Male; Mice; Myocardium/metabolism*; Neovascularization, Pathologic/genetics; Neovascularization, Pathologic/metabolism; Sequence Analysis, RNA*; Sodium/metabolism; Vasodilation

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