4.7 Article

The Bicarbonate Transporter SLC4A7 Plays a Key Role in Macrophage Phagosome Acidification

Journal

CELL HOST & MICROBE
Volume 23, Issue 6, Pages 766-+

Publisher

CELL PRESS
DOI: 10.1016/j.chom.2018.04.013

Keywords

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Funding

  1. Austrian Academy of Sciences
  2. Austrian Science Fund [FWF I2192-B22 ERASE, FWF F4711-B20, FWF P29250-B30 VITRA, FWF W1205 DK CCHD]
  3. European Research Council [ERC AdG 695214]
  4. European Molecular Biology Organization (EMBO Long-Term Fellowship) [ALTF245-2017]
  5. Boehringer Ingelheim [BI-CeMM 238114]
  6. European Commission (Marie Sklodowska-Curie Action Fellowship) [661491]

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Macrophages represent the first line of immune defense against pathogens, and phagosome acidification is a necessary step in pathogen clearance. Here, we identified the bicarbonate transporter SLC4A7, which is strongly induced upon macrophage differentiation, as critical for phagosome acidification. Loss of SLC4A7 reduced acidification of phagocytosed beads or bacteria and impaired the intracellular microbicidal capacity in human macrophage cell lines. The phenotype was rescued by wild-type SLC4A7, but not by SLC4A7 mutants, affecting transport capacity or cell surface localization. Loss of SLC4A7 resulted in increased cytoplasmic acidification during phagocytosis, suggesting that SLC4A7-mediated, bicarbonate-driven maintenance of cytoplasmic pH is necessary for phagosome acidification. Altogether, we identify SLC4A7 and bicarbonate-driven cytoplasmic pH homeostasis as an important element of phagocytosis and the associated microbicidal functions in macrophages.

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