Figure 1.
Chloride is the predominant anion that regulates phagosomal oxidant production in PMN phagosomes. NADPH oxidase transfers electrons into the phagosomal lumen, thereby creating a transmembrane potential that activates voltage-gated proton channels, such as Hv1, to conduct an influx of protons. In addition, the ATP-driven proton pump vacuolar-type ATPase (V-ATPase) actively pumps protons in the same direction. Other cations such as K+, Na+, and Ca2+ can be transported into phagosomes via monovalent or divalent cation/H+ exchangers, or K+/Cl‒ symporter. To counterbalance the influx of the cations, Cl‒ is transported through chloride channels, including CFTR, CaCC, and voltage-gated ClCs.

Chloride is the predominant anion that regulates phagosomal oxidant production in PMN phagosomes. NADPH oxidase transfers electrons into the phagosomal lumen, thereby creating a transmembrane potential that activates voltage-gated proton channels, such as Hv1, to conduct an influx of protons. In addition, the ATP-driven proton pump vacuolar-type ATPase (V-ATPase) actively pumps protons in the same direction. Other cations such as K+, Na+, and Ca2+ can be transported into phagosomes via monovalent or divalent cation/H+ exchangers, or K+/Cl symporter. To counterbalance the influx of the cations, Cl is transported through chloride channels, including CFTR, CaCC, and voltage-gated ClCs.

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