Anion Exchanger 2 Regulates Dectin-1-Dependent Phagocytosis and Killing of Candida albicans

Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl-/HCO3- exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytop...

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Published inPloS one Vol. 11; no. 7; p. e0158893
Main Authors Urso, Katia, Charles, Julia F., Shull, Gary E., Aliprantis, Antonios O., Balestrieri, Barbara
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 08.07.2016
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Abstract Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl-/HCO3- exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytoplasmic pH and electroneutrality during acid secretion. Macrophages require endosomal acidification for pathogen killing during the process known as phagocytosis. Chloride is thought to be the principal ion responsible for maintaining electroneutrality during organelle acidification, but whether Cl-/HCO3- exchangers such as Ae2 contribute to macrophage function is not known. In this study we investigated the role of Ae2 in primary macrophages during phagocytosis. We find that Ae2 is expressed in macrophages where it regulates intracellular pH and the binding of Zymosan, a fungal cell wall derivative. Surprisingly, the transcription and surface expression of Dectin-1, the major phagocytic receptor for Candida albicans (C. albicans) and Zymosan, is reduced in the absence of Ae2. As a consequence, Zymosan-induced Tnfα expression is also impaired in Ae2-deficient macrophages. Similar to Ae2 deficiency, pharmacological alkalinization of lysosomal pH with bafilomycin A decreases both Dectin-1 mRNA and cell surface expression. Finally, Ae2-deficient macrophages demonstrate defective phagocytosis and killing of the human pathogenic fungus C. albicans. Our results strongly suggest that Ae2 is a critical factor in the innate response to C. albicans. This study represents an important contribution to a better understanding of how Dectin-1 expression and fungal clearance is regulated.
AbstractList Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl-/HCO3- exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytoplasmic pH and electroneutrality during acid secretion. Macrophages require endosomal acidification for pathogen killing during the process known as phagocytosis. Chloride is thought to be the principal ion responsible for maintaining electroneutrality during organelle acidification, but whether Cl-/HCO3- exchangers such as Ae2 contribute to macrophage function is not known. In this study we investigated the role of Ae2 in primary macrophages during phagocytosis. We find that Ae2 is expressed in macrophages where it regulates intracellular pH and the binding of Zymosan, a fungal cell wall derivative. Surprisingly, the transcription and surface expression of Dectin-1, the major phagocytic receptor for Candida albicans (C. albicans) and Zymosan, is reduced in the absence of Ae2. As a consequence, Zymosan-induced Tnfα expression is also impaired in Ae2-deficient macrophages. Similar to Ae2 deficiency, pharmacological alkalinization of lysosomal pH with bafilomycin A decreases both Dectin-1 mRNA and cell surface expression. Finally, Ae2-deficient macrophages demonstrate defective phagocytosis and killing of the human pathogenic fungus C. albicans. Our results strongly suggest that Ae2 is a critical factor in the innate response to C. albicans. This study represents an important contribution to a better understanding of how Dectin-1 expression and fungal clearance is regulated.
Anion exchanger 2 (Ae2; gene symbol, Slc4a2 ) is a plasma membrane Cl - /HCO 3 - exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytoplasmic pH and electroneutrality during acid secretion. Macrophages require endosomal acidification for pathogen killing during the process known as phagocytosis. Chloride is thought to be the principal ion responsible for maintaining electroneutrality during organelle acidification, but whether Cl - /HCO 3 - exchangers such as Ae2 contribute to macrophage function is not known. In this study we investigated the role of Ae2 in primary macrophages during phagocytosis. We find that Ae2 is expressed in macrophages where it regulates intracellular pH and the binding of Zymosan, a fungal cell wall derivative. Surprisingly, the transcription and surface expression of Dectin-1 , the major phagocytic receptor for Candida albicans ( C . albicans ) and Zymosan, is reduced in the absence of Ae2. As a consequence, Zymosan-induced Tnfα expression is also impaired in Ae2- deficient macrophages. Similar to Ae2 deficiency, pharmacological alkalinization of lysosomal pH with bafilomycin A decreases both Dectin-1 mRNA and cell surface expression. Finally, Ae2- deficient macrophages demonstrate defective phagocytosis and killing of the human pathogenic fungus C . albicans . Our results strongly suggest that Ae2 is a critical factor in the innate response to C . albicans . This study represents an important contribution to a better understanding of how Dectin-1 expression and fungal clearance is regulated.
Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl.sup.- /HCO.sub.3 .sup.- exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytoplasmic pH and electroneutrality during acid secretion. Macrophages require endosomal acidification for pathogen killing during the process known as phagocytosis. Chloride is thought to be the principal ion responsible for maintaining electroneutrality during organelle acidification, but whether Cl.sup.- /HCO.sub.3 .sup.- exchangers such as Ae2 contribute to macrophage function is not known. In this study we investigated the role of Ae2 in primary macrophages during phagocytosis. We find that Ae2 is expressed in macrophages where it regulates intracellular pH and the binding of Zymosan, a fungal cell wall derivative. Surprisingly, the transcription and surface expression of Dectin-1, the major phagocytic receptor for Candida albicans (C. albicans) and Zymosan, is reduced in the absence of Ae2. As a consequence, Zymosan-induced Tnf[alpha] expression is also impaired in Ae2-deficient macrophages. Similar to Ae2 deficiency, pharmacological alkalinization of lysosomal pH with bafilomycin A decreases both Dectin-1 mRNA and cell surface expression. Finally, Ae2-deficient macrophages demonstrate defective phagocytosis and killing of the human pathogenic fungus C. albicans. Our results strongly suggest that Ae2 is a critical factor in the innate response to C. albicans. This study represents an important contribution to a better understanding of how Dectin-1 expression and fungal clearance is regulated.
Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl-/HCO3- exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytoplasmic pH and electroneutrality during acid secretion. Macrophages require endosomal acidification for pathogen killing during the process known as phagocytosis. Chloride is thought to be the principal ion responsible for maintaining electroneutrality during organelle acidification, but whether Cl-/HCO3- exchangers such as Ae2 contribute to macrophage function is not known. In this study we investigated the role of Ae2 in primary macrophages during phagocytosis. We find that Ae2 is expressed in macrophages where it regulates intracellular pH and the binding of Zymosan, a fungal cell wall derivative. Surprisingly, the transcription and surface expression of Dectin-1, the major phagocytic receptor for Candida albicans (C. albicans) and Zymosan, is reduced in the absence of Ae2. As a consequence, Zymosan-induced Tnf[alpha] expression is also impaired in Ae2-deficient macrophages. Similar to Ae2 deficiency, pharmacological alkalinization of lysosomal pH with bafilomycin A decreases both Dectin-1 mRNA and cell surface expression. Finally, Ae2-deficient macrophages demonstrate defective phagocytosis and killing of the human pathogenic fungus C. albicans. Our results strongly suggest that Ae2 is a critical factor in the innate response to C. albicans. This study represents an important contribution to a better understanding of how Dectin-1 expression and fungal clearance is regulated.
Anion exchanger 2 (Ae2; gene symbol, Slc4a2 ) is a plasma membrane Cl - /HCO 3 - exchanger expressed in the gastrointestinal tract, kidney and bone. We have previously shown that Ae2 is required for the function of osteoclasts, bone resorbing cells of the macrophage lineage, to maintain homeostatic cytoplasmic pH and electroneutrality during acid secretion. Macrophages require endosomal acidification for pathogen killing during the process known as phagocytosis. Chloride is thought to be the principal ion responsible for maintaining electroneutrality during organelle acidification, but whether Cl - /HCO 3 - exchangers such as Ae2 contribute to macrophage function is not known. In this study we investigated the role of Ae2 in primary macrophages during phagocytosis. We find that Ae2 is expressed in macrophages where it regulates intracellular pH and the binding of Zymosan, a fungal cell wall derivative. Surprisingly, the transcription and surface expression of Dectin-1 , the major phagocytic receptor for Candida albicans ( C . albicans ) and Zymosan, is reduced in the absence of Ae2. As a consequence, Zymosan-induced Tnfα expression is also impaired in Ae2- deficient macrophages. Similar to Ae2 deficiency, pharmacological alkalinization of lysosomal pH with bafilomycin A decreases both Dectin-1 mRNA and cell surface expression. Finally, Ae2- deficient macrophages demonstrate defective phagocytosis and killing of the human pathogenic fungus C . albicans . Our results strongly suggest that Ae2 is a critical factor in the innate response to C . albicans . This study represents an important contribution to a better understanding of how Dectin-1 expression and fungal clearance is regulated.
Audience Academic
Author Aliprantis, Antonios O.
Urso, Katia
Balestrieri, Barbara
Charles, Julia F.
Shull, Gary E.
AuthorAffiliation 1 Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women’s, Hospital and Harvard Medical School, Boston, Massachusetts, United States of America
3 Jeff and Penny Vinik Center for Allergic Disease Research, Division of Rheumatology, Immunology and Allergy, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, United States of America
University of Birmingham, UNITED KINGDOM
2 Department of Molecular Genetics, University of Cincinnati College of Medicine, Cincinnati, Ohio, United States of America
AuthorAffiliation_xml – name: 1 Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women’s, Hospital and Harvard Medical School, Boston, Massachusetts, United States of America
– name: 2 Department of Molecular Genetics, University of Cincinnati College of Medicine, Cincinnati, Ohio, United States of America
– name: 3 Jeff and Penny Vinik Center for Allergic Disease Research, Division of Rheumatology, Immunology and Allergy, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, United States of America
– name: University of Birmingham, UNITED KINGDOM
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  surname: Urso
  fullname: Urso, Katia
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  fullname: Aliprantis, Antonios O.
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  fullname: Balestrieri, Barbara
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27391897$$D View this record in MEDLINE/PubMed
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2016 Urso et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Conceived and designed the experiments: KU AOA BB. Performed the experiments: KU BB. Analyzed the data: KU BB. Contributed reagents/materials/analysis tools: GS. Wrote the paper: KU JC GS AOA BB.
Competing Interests: The authors have declared that no competing interests exist.
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SSID ssj0053866
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Snippet Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl-/HCO3- exchanger expressed in the gastrointestinal tract, kidney and bone. We have...
Anion exchanger 2 (Ae2; gene symbol, Slc4a2) is a plasma membrane Cl.sup.- /HCO.sub.3 .sup.- exchanger expressed in the gastrointestinal tract, kidney and...
Anion exchanger 2 (Ae2; gene symbol, Slc4a2 ) is a plasma membrane Cl - /HCO 3 - exchanger expressed in the gastrointestinal tract, kidney and bone. We have...
Anion exchanger 2 (Ae2; gene symbol, Slc4a2 ) is a plasma membrane Cl - /HCO 3 - exchanger expressed in the gastrointestinal tract, kidney and bone. We have...
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SourceType Open Website
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StartPage e0158893
SubjectTerms Acidification
Animals
Anion exchanging
Bafilomycin A
Biocompatibility
Biology and Life Sciences
Biomedical materials
Candida
Candida albicans
Candida albicans - immunology
Candidiasis - genetics
Candidiasis - immunology
Cell surface
Cell walls
Chloride
Chloride-Bicarbonate Antiporters - genetics
Chloride-Bicarbonate Antiporters - immunology
Chlorides
Cytokines
Fungal infections
Fungi
Gastrointestinal tract
Gene expression
Genetic aspects
Hospitals
Immune system
Immunology
Ion exchangers
Lectins, C-Type - genetics
Lectins, C-Type - immunology
Macrophages
Macrophages, Peritoneal - immunology
Medical schools
Medicine
Medicine and Health Sciences
Mice
Mice, Knockout
Osteoclasts
Pathogens
pH effects
Phagocytes
Phagocytosis
Phagocytosis - immunology
Pharmacology
Physical Sciences
Physiological aspects
Research and Analysis Methods
Rheumatology
Rodents
Secretion
Transcription
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Title Anion Exchanger 2 Regulates Dectin-1-Dependent Phagocytosis and Killing of Candida albicans
URI https://www.ncbi.nlm.nih.gov/pubmed/27391897
https://www.proquest.com/docview/1802588996
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https://pubmed.ncbi.nlm.nih.gov/PMC4938408
https://doaj.org/article/11a75978f0cd4f69a0dcdb0a5439d373
http://dx.doi.org/10.1371/journal.pone.0158893
Volume 11
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