Published online
doi:10.1085/jgp.200810169
The Journal of General Physiology, Vol. 133, No. 6, 603-622
The Rockefeller University Press, 0022-1295 $30.00
© Adijanto et al.
CO2-induced ion and fluid transport in human retinal pigment epithelium
Jeffrey Adijanto1,2,
Tina Banzon2,
Stephen Jalickee2,
Nam S. Wang1, and
Sheldon S. Miller2
1 Department of Chemical and Biomolecular Engineering, The University of Maryland, College Park, MD 20742
2 National Institutes of Health, National Eye Institute, Bethesda, MD 20892
Correspondence to Sheldon S. Miller: millers{at}nei.nih.gov
In the intact eye, the transition from light to dark alters pH, [Ca2+], and [K] in the subretinal space (SRS) separating the photoreceptor outer segments and the apical membrane of the retinal pigment epithelium (RPE). In addition to these changes, oxygen consumption in the retina increases with a concomitant release of CO2 and H2O into the SRS. The RPE maintains SRS pH and volume homeostasis by transporting these metabolic byproducts to the choroidal blood supply. In vitro, we mimicked the transition from light to dark by increasing apical bath CO2 from 5 to 13%; this maneuver decreased cell pH from 7.37 ± 0.05 to 7.14 ± 0.06 (n = 13). Our analysis of native and cultured fetal human RPE shows that the apical membrane is significantly more permeable (
10-fold; n = 7) to CO2 than the basolateral membrane, perhaps due to its larger exposed surface area. The limited CO2 diffusion at the basolateral membrane promotes carbonic anhydrase–mediated HCO3 transport by a basolateral membrane Na/nHCO3 cotransporter. The activity of this transporter was increased by elevating apical bath CO2 and was reduced by dorzolamide. Increasing apical bath CO2 also increased intracellular Na from 15.7 ± 3.3 to 24.0 ± 5.3 mM (n = 6; P < 0.05) by increasing apical membrane Na uptake. The CO2-induced acidification also inhibited the basolateral membrane Cl/HCO3 exchanger and increased net steady-state fluid absorption from 2.8 ± 1.6 to 6.7 ± 2.3 µl x cm–2 x hr–1 (n = 5; P < 0.05). The present experiments show how the RPE can accommodate the increased retinal production of CO2 and H2O in the dark, thus preventing acidosis in the SRS. This homeostatic process would preserve the close anatomical relationship between photoreceptor outer segments and RPE in the dark and light, thus protecting the health of the photoreceptors.
Abbreviations used in this paper: AQP1, aquaporin 1; CA, carbonic anhydrase; CPE, choroid plexus epithelium; CSF, cerebrospinal fluid; DIDS, 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid; DZA, dorzolamide; ENBC, reversal potential of NBC; hfRPE, human fetal retinal pigment epithelium; JV, steady-state fluid absorption rate; pHi, intracellular pH; RPE, retinal pigment epithelium; RT, total tissue resistance; SRS, subretinal space; TEP, transepithelial potential.
This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jgp.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

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