Effect of expressing the water channel aquaporin-1 on the CO2 permeability ofXenopus oocytes

NL Nakhoul, BA Davis, MF Romero… - American Journal of …, 1998 - journals.physiology.org
NL Nakhoul, BA Davis, MF Romero, WF Boron
American Journal of Physiology-Cell Physiology, 1998journals.physiology.org
It is generally accepted that gases such as CO2 cross cell membranes by dissolving in the
membrane lipid. No role for channels or pores in gas transport has ever been demonstrated.
Here we ask whether expression of the water channel aquaporin-1 (AQP1) enhances the
CO2 permeability of Xenopus oocytes. We expressed AQP1 in Xenopus oocytes by injecting
AQP1 cRNA, and we assessed CO2permeability by using microelectrodes to monitor the
changes in intracellular pH (pHi) produced by adding 1.5% CO2/10 mM HCO 3− to (or …
It is generally accepted that gases such as CO2 cross cell membranes by dissolving in the membrane lipid. No role for channels or pores in gas transport has ever been demonstrated. Here we ask whether expression of the water channel aquaporin-1 (AQP1) enhances the CO2 permeability ofXenopus oocytes. We expressed AQP1 inXenopus oocytes by injecting AQP1 cRNA, and we assessed CO2permeability by using microelectrodes to monitor the changes in intracellular pH (pHi) produced by adding 1.5% CO2/10 mM to (or removing it from) the extracellular solution. Oocytes normally have an undetectably low level of carbonic anhydrase (CA), which eliminates the CO2 hydration reaction as a rate-limiting step. We found that expressing AQP1 (vs. injecting water) had no measurable effect on the rate of CO2-induced pHi changes in such low-CA oocytes: adding CO2 caused pHi to fall at a mean initial rate of 11.3 × 10−4 pH units/s in control oocytes and 13.3 × 10−4 pH units/s in oocytes expressing AQP1. When we injected oocytes with water, and a few days later with CA, the CO2-induced pHi changes in these water/CA oocytes were more than fourfold faster than in water-injected oocytes (acidification rate, 53 × 10−4 pH units/s). Ethoxzolamide (ETX; 10 μM), a membrane-permeant CA inhibitor, greatly slowed the pHi changes (16.5 × 10−4 pH units/s). When we injected oocytes with AQP1 cRNA and then CA, the CO2-induced pHi changes in these AQP1/CA oocytes were ∼40% faster than in the water/CA oocytes (75 × 10−4 pH units/s), and ETX reduced the rates substantially (14.7 × 10−4 pH units/s). Thus, in the presence of CA, AQP1 expression significantly increases the CO2 permeability of oocyte membranes. Possible explanations include1) AQP1 expression alters the lipid composition of the cell membrane, 2) AQP1 expression causes overexpression of a native gas channel, and/or 3) AQP1 acts as a channel through which CO2 can permeate. Even if AQP1 should mediate a CO2 flux, it would remain to be determined whether this CO2movement is quantitatively important.
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