Concentration-Dependent Effects on Intracellular and Surface pH of Exposing Xenopus oocytes to Solutions Containing NH3/NH4 +
- 26 February 2009
- journal article
- research article
- Published by Springer Nature in The Journal of Membrane Biology
- Vol. 228 (1) , 15-31
- https://doi.org/10.1007/s00232-009-9155-7
Abstract
Others have shown that exposing oocytes to high levels of \( {\text{NH}}_{ 3} /{\text{NH}}_{ 4}{}^{ + } \)(10–20 mM) causes a paradoxical fall in intracellular pH (pHi), whereas low levels (e.g., 0.5 mM) cause little pHi change. Here we monitored pHi and extracellular surface pH (pHS) while exposing oocytes to 5 or 0.5 mM NH3/NH4 +. We confirm that 5 mM \( {\text{NH}}_{ 3} /{\text{NH}}_{ 4}{}^{ + } \) causes a paradoxical pHi fall (−ΔpHi ≅ 0.2), but also observe an abrupt pHS fall (−ΔpHS ≅ 0.2)—indicative of NH3 influx—followed by a slow decay. Reducing [NH3/NH4 +] to 0.5 mM minimizes pHi changes but maintains pHS changes at a reduced magnitude. Expressing AmtB (bacterial Rh homologue) exaggerates −ΔpHS at both \( {\text{NH}}_{ 3} /{\text{NH}}_{ 4}{}^{ + } \) levels. During removal of 0.5 or 5 mM NH3/NH4 +, failure of pHS to markedly overshoot bulk extracellular pH implies little NH3 efflux and, thus, little free cytosolic NH3/NH4 +. A new analysis of the effects of NH3 vs. NH4 + fluxes on pHS and pHi indicates that (a) NH3 rather than NH4 + fluxes dominate pHi and pHS changes and (b) oocytes dispose of most incoming NH3. NMR studies of oocytes exposed to 15N-labeled \( {\text{NH}}_{ 3} /{\text{NH}}_{ 4}{}^{ + } \) show no significant formation of glutamine but substantial \( {\text{NH}}_{ 3} /{\text{NH}}_{ 4}{}^{ + } \) accumulation in what is likely an acid intracellular compartment. In conclusion, parallel measurements of pHi and pHS demonstrate that NH3 flows across the plasma membrane and provide new insights into how a protein molecule in the plasma membrane—AmtB—enhances the flux of a gas across a biological membrane.
Keywords
This publication has 48 references indexed in Scilit:
- Relative CO 2 /NH 3 selectivities of AQP1, AQP4, AQP5, AmtB, and RhAGProceedings of the National Academy of Sciences, 2009
- Subcellular localization of ammonium transporters in Dictyostelium discoideumBMC Cell Biology, 2008
- Characterization of Human SLC4A10 as an Electroneutral Na/HCO3 Cotransporter (NBCn2) with Cl– Self-exchange ActivityJournal of Biological Chemistry, 2008
- The crystal structure of the Escherichia coli AmtB–GlnK complex reveals how GlnK regulates the ammonia channelProceedings of the National Academy of Sciences, 2007
- Function of Ammonium Transporter A in the Initiation of Culmination of Development in Dictyostelium discoideumEukaryotic Cell, 2006
- Crystal structure of the archaeal ammonium transporter Amt-1 from Archaeoglobus fulgidusProceedings of the National Academy of Sciences, 2005
- The mechanism of ammonia transport based on the crystal structure of AmtB of Escherichia coliProceedings of the National Academy of Sciences, 2004
- Mechanism of Ammonia Transport by Amt/MEP/Rh: Structure of AmtB at 1.35 ÅScience, 2004
- Direct measurement of intracellular pH changes in Xenopus eggs at fertilization and cleavage.The Journal of cell biology, 1981
- Active proton transport stimulated by CO2/HCO3−, blocked by cyanideNature, 1976