The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
Stoichiometry and Ion Dependencies of the Intracellular-pH-Regulating Mechanism in Squid Giant Axons
Open accessAbstract
The ion transport system responsible for intracellular pH (pHi) regulation in squid giant axons was examined in experiments with pH-sensitive microelectrodes and isotopic fluxes of Na+ and Cl-. In one study, axons were acid-loaded and the rate of the subsequent pHi recovery was used to calculate the acid extrusion rate. There was an absolute dependence of acid extrusion on external Na+, external HCO-3 (at constant pH), and internal Cl-. Furthermore, the dependence of the acid extrusion rate on each of these three parameters was described by Michaelis-Menten kinetics. Acid extrusion was stimulated by an acid pHi, required internal ATP, and was blocked by external 4-acetamido-4'-isothiocyanostilbene-2,2'-disulfonate (SITS). Under a standard set of conditions (i.e., [HCO-3]o = 12 mM, pHo = 8.00, [Na+]o = 425 mM, [Cl-]i = 150 mM, [ATP]i = 4 mM, pHi = 6.5, and 16 degrees C), the mean acid extrusion rate was 7.5 pmol X cm-2 X s-1. In a second study under the above standard conditions, the unidirectional Na+ efflux (measured with 22Na) mediated by the pHi-regulating system was found to be approximately 0, whereas the mean influx was about 3.4 pmol X cm-2 X s-1. This net influx required external HCO-3, internal Cl-, and acid pHi, internal ATP, and was blocked by SITS. In the final series of experiments under the above standard conditions, the unidirectional Cl- influx (measured with 36Cl) mediated by the pHi-regulating system was found to be approximately 0, whereas the mean efflux was approximately 3.9 pmol X cm-2 X s-1. This net efflux required external HCO-3, external Na+, an acid pHi, internal ATP, and was blocked by SITS. We conclude that the pHi-regulating system mediates the obligate net influx of HCO-3 (or equivalent species) and Na+ and the net efflux of Cl- in the stoichiometry of 2:1:1. The transport system is stimulated by intracellular acid loads, requires ATP, and is blocked by SITS.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“However, such mechanisms (e.g., Na+/H+ antiporters or histone deacetylation) consume cellular energy and can alter gene transcription and reduce cellular growth through changes in the acetylation state of chromatin (Boron and Russell, 1983; Bowen and Levinson, 1984; Boron, 2004).”
From Toward Best Practices for Controlling Mammalian Cell Culture Environments (2022) · cites this paper as Boron and Russell, 1983
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Roos, A., & Boron, W. F. (1981) · Physiological Reviews · doi:10.1152/physrev.1981.61.2.296 · Cited by 2,511
Self-citationIntracellular pH transients in squid giant axons caused by CO2, NH3, and metabolic inhibitors.
Boron, W. F., & Weer, P. D. (1976) · The Journal of General Physiology · doi:10.1085/jgp.67.1.91 · Cited by 921
Self-citationTHOMAS, R. C. (1977) · The Journal of Physiology · doi:10.1113/jphysiol.1977.sp012096 · Cited by 369
Cala, P. M. (1980) · The Journal of General Physiology · doi:10.1085/jgp.76.6.683 · Cited by 354
Role of chloride transport in regulation of intracellular pH
Russell, J. M., & Boron, W. F. (1976) · Nature · doi:10.1038/264073a0 · Cited by 224
Self-citationVaughan‐Jones, R. D. (1979) · The Journal of Physiology · doi:10.1113/jphysiol.1979.sp012957 · Cited by 175
Chloride in the squid giant axon
Keynes, R. D. (1963) · The Journal of Physiology · doi:10.1113/jphysiol.1963.sp007289 · Cited by 172
pH regulation in barnacle muscle fibers: dependence on intracellular and extracellular pH
Boron, W. F., McCormick, W. C., & Roos, A. D. G. D. (1979) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1979.237.3.c185 · Cited by 149
Self-citationThe ionic mechanism of intracellular pH regulation in crayfish neurones.
Moody, W. J. (1981) · The Journal of Physiology · doi:10.1113/jphysiol.1981.sp013788 · Cited by 135
Ionic mechanism of the H+ pump in a snail neurone
THOMAS, R. C. (1976) · Nature · doi:10.1038/262054a0 · Cited by 124
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–169 of 169
K(+)- and HCO3(-)-dependent acid-base transport in squid giant axons. I. Base efflux.
Hogan, E. M., Cohen, M. A., & Boron, W. F. (1995) · The Journal of General Physiology · doi:10.1085/jgp.106.5.821 · Cited by 26
Self-citationSalameh, A., Hübner, C. A., & Boron, W. F. (2016) · The Journal of Physiology · doi:10.1113/jp272470 · Cited by 24
Self-citationLee, S., Occhipinti, R., Moss, F. J., Parker, M. D., Grichtchenko, I. I., & Boron, W. F. (2022) · Journal of the American Society of Nephrology · doi:10.1681/asn.2022030289 · Cited by 25
Self-citationPiermarini, P. M., Choi, I., & Boron, W. F. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00544.2006 · Cited by 25
Self-citationChen, L., Haddad, G. G., & Boron, W. F. (2008) · Brain Research · doi:10.1016/j.brainres.2008.08.033 · Cited by 25
Self-citationOlsnes, S., & Sandvig, K. (1986) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)35974-4 · Cited by 24
Toward Best Practices for Controlling Mammalian Cell Culture Environments
Klein, S. G., Steckbauer, A., Alsolami, S. M., Arossa, S., Parry, A. J., Li, M., & Duarte, C. M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.788808 · Cited by 23
Fitzgerald, E. M., Djamgoz, M. B. A., & Dunbar, S. J. (1996) · Journal of Experimental Biology · doi:10.1242/jeb.199.8.1857 · Cited by 23
Bonanno, J. A., & Machen, T. E. (1989) · Experimental Eye Research · doi:10.1016/0014-4835(89)90081-x · Cited by 23
Chloride in the Squid Giant Axon
Russell, J. M. (1984) · Current topics in membranes and transport · doi:10.1016/s0070-2161(08)60471-2 · Cited by 22
Self-citationBrooks, K. J., Kauppinen, R. A., Williams, S. R., Bachelard, H. S., Bate, T. E., & Gadian, D. G. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90320-5 · Cited by 22
Ellington, W. R. (1993) · Biological Bulletin · doi:10.2307/1542228 · Cited by 21
Chesler, M. (1987) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y87-156 · Cited by 21
Deitmer, J. W., & Schneider, H. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.459be.x · Cited by 21
Stimulation of Cl- self exchange by intracellular HCO3- in rabbit cortical collecting duct
Matsuzaki, K., Stokes, J. B., & Schuster, V. L. (1989) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1989.257.1.c94 · Cited by 21
Chapter 12 Na+-H+ Exchange and Growth Control in Fibroblasts: A Genetic Approach
Pouysségur, J., Franchi, A. J., Kohno, M., L’Allemain, G., & Paris, S. (1986) · Current topics in membranes and transport · doi:10.1016/s0070-2161(08)60734-0 · Cited by 20
Moss, F. J., & Boron, W. F. (2020) · The Journal of Physiology · doi:10.1113/jp280143 · Cited by 18
Self-citationpH regulation in non-neuronal brain cells and interstitial fluid
McAlear, S. D., & Bevensee, M. O. (2003) · Advances in molecular and cell biology · doi:10.1016/s1569-2558(03)31032-x · Cited by 18
Okada, M., Saito, Y., Sawada, E., & Nishiyama, A. (1991) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00371116 · Cited by 18
Russell, J. M., & Brodwick, M. S. (1988) · The Journal of General Physiology · doi:10.1085/jgp.91.4.495 · Cited by 18
Self-citationCytoplasmic pH regulation in canine renal proximal tubule cells
Reid, I. R., Civitelli, R., Westbrook, S., Avioli, L. V., & Hruska, K. A. (1987) · Kidney International · doi:10.1038/ki.1987.116 · Cited by 17
Acid influx into snail neurones caused by reversal of the normal pHi‐regulating system.
Evans, M. G., & THOMAS, R. C. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015012 · Cited by 16
Glial H+ Transport and Control of pH
Schlue, W. R., DÖRNER, R., Rempe, L., & Riehl, B. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb15621.x · Cited by 15
Putnam, R. W., & Roos, A. (1997) · Comprehensive physiology · doi:10.1002/cphy.cp140109 · Cited by 15
Potential Novel Role of Membrane-Associated Carbonic Anhydrases in the Kidney
Lee, S., Boron, W. F., & Occhipinti, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24044251 · Cited by 13
Self-citationpH Regulation in Horizontal Cells of the Skate Retina
Haugh-Scheidt, L. M., & Ripps, H. (1998) · Experimental Eye Research · doi:10.1006/exer.1997.0441 · Cited by 13
The mechanisms of sodium current inhibition by benzocaine in the squid giant axon
Elliott, J. R., Haydon, D. A., & Hendry, B. M. (1987) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00584659 · Cited by 13
Guggino, W. B., & Guggino, S. E. (1989) · Kidney International · doi:10.1038/ki.1989.207 · Cited by 13
Extracellular magnesium-dependent sodium efflux in squid giant axons
Gonzalez-Serratos, H., & Rasgado-Flores, H. (1990) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1990.259.4.c541 · Cited by 13
Bevensee, M. O., & Boron, W. F. (2008) · Elsevier eBooks · doi:10.1016/b978-012088488-9.50054-1 · Cited by 12
Self-citationAcid pH and weak acids induce Na−Cl contransport in the rabbit urinary bladder
Ifshin, M. S., Johnson, K. E., & Eaton, D. C. (1983) · The Journal of Membrane Biology · doi:10.1007/bf02000615 · Cited by 12
Inhibition of K/HCO 3 Cotransport in Squid Axons by Quaternary Ammonium Ions
Davis, B. A., Hogan, E. M., Cooper, G. J., Bashi, E., Zhao, J., & Boron, W. F. (2001) · The Journal of Membrane Biology · doi:10.1007/s00232-001-0050-0 · Cited by 10
Self-citationA role for Na + /H + exchange in pH regulation in Helix neurones
Willoughby, D., THOMAS, R. C., & Schwiening, C. J. (1999) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240051101 · Cited by 11
Baumgarten, C. M., & Duncan, S. W. N. (1987) · Developments in cardiovascular medicine · doi:10.1007/978-1-4613-2053-1_7 · Cited by 11
Expression of a mammalian Na–H exchanger in muscle fibres of the giant barnacle
Knakal, R. C., Summers, W. C., Cragoe, E. J., & Boron, W. F. (1985) · Nature · doi:10.1038/315756a0 · Cited by 10
Self-citationGABA-Activated Bicarbonate Conductance
Kaila, K., & Voipio, J. (1990) · Springer eBooks · doi:10.1007/978-1-4757-9685-8_12 · Cited by 9
A “Post-copernican” Analysis of Intracellular pH
Magder, S. A. (2002) · Springer eBooks · doi:10.1007/978-88-470-2099-3_50 · Cited by 9
Lithium transport across squid axon membrane
Ehrlich, B. E., & Russell, J. M. (1984) · Brain Research · doi:10.1016/0006-8993(84)91406-9 · Cited by 9
Self-citationThe Role of Extracellular Sodium in the Mechanism of A Neuronal in Vitro Circadian Pacemaker
Khalsa, S. B. S., Michel, S., & Block, G. D. (1997) · Chronobiology International · doi:10.3109/07420529709040536 · Cited by 8
Does low intracellular pH stop the motion of the Bulla circadian pacemaker?
Khalsa, S. B. S., Ralph, M., & Block, G. D. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-09-02672.1991 · Cited by 8
Carriers, exchangers, and cotransporters in the first 100 years of the Journal of General Physiology
Jennings, M. L. (2018) · The Journal of General Physiology · doi:10.1085/jgp.201812078 · Cited by 7
THOMAS, R. C. (1995) · Nature · doi:10.1038/374597a0 · Cited by 7
Chloride Transport in the Squid Giant Axon
Russell, J. M., & Boron, W. F. (1990) · Springer eBooks · doi:10.1007/978-1-4757-9685-8_3 · Cited by 7
Self-citationIntracellular Ionized Calcium Changes in Squid Giant Axons Monitored by Fura‐2 and Aequorina
Requena, J., Whittembury, J., Scarpa, A., BRINLEY, J. F., & Mullins, L. J. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb17295.x · Cited by 6
Dobrowsky, E., Newell, K. J., & Tannock, I. F. (1991) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/0360-3016(91)90104-c · Cited by 6
Boron, W. F. (1986) · Springer eBooks · doi:10.1007/978-1-4613-2097-5_26 · Cited by 5
Self-citationRomero, M. F., Chang, M.-H., & Mount, D. B. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374373-2.00004-2 · Cited by 4
Evidence for a exchange system in the mammalian lens
Duncan, G., Dart, C., Croghan, P. C., & Gandolfi, S. (1992) · Experimental Eye Research · doi:10.1016/0014-4835(92)90158-o · Cited by 4
Changes in internal ionized Ca2+ and H+ in voltage clamped squid axons
Mullins, L. J., Whittembury, J., & Requena, J. (1989) · Cell Calcium · doi:10.1016/0143-4160(89)90031-6 · Cited by 4
Moe, O. W., & Alpern, R. J. (1996) · Springer eBooks · doi:10.1007/978-1-4613-1143-0_20 · Cited by 4
Chapter 3 Aspects of pHi Regulation in Frog Skeletal Muscle
Putnam, R. W., & Roos, A. (1986) · Current topics in membranes and transport · doi:10.1016/s0070-2161(08)60725-x · Cited by 4
Chapter 1 Intracellular pH Regulation by Leech and Other Invertebrate Neurons
THOMAS, R. C., & Schlue, W. R. (1986) · Current topics in membranes and transport · doi:10.1016/s0070-2161(08)60723-6 · Cited by 4
Bouyer, P. G., Salameh, A., Zhou, Y., Kolba, T. N., & Boron, W. F. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2024.1434359 · Cited by 3
Self-citationBouyer, P. G., Occhipinti, R., Taki, S., Moss, F. J., & Boron, W. F. (2025) · Frontiers in Physiology · doi:10.3389/fphys.2024.1494956 · Cited by 2
Self-citationATP Dependence of Na+-Driven Cl–HCO3 Exchange in Squid Axons
Davis, B. A., Hogan, E. M., Russell, J. M., & Boron, W. F. (2008) · The Journal of Membrane Biology · doi:10.1007/s00232-008-9100-1 · Cited by 2
Self-citationIntracellular pH regulation in isolated hepatopancreas cells from the roman snail (Helix pomatia)
Manzl, C., Krumschnabel, G., Schwarzbaum, P. J., Chabicovsky, M., & Dallinger, R. (2003) · Journal of Experimental Zoology Part A Comparative Experimental Biology · doi:10.1002/jez.a.20001 · Cited by 2
Rector, F. C. (1987) · Springer eBooks · doi:10.1007/978-1-4614-7545-3_11 · Cited by 2
Characterization of the Na+/H+ antiporter in cells of the mussel Mytilus galloprovincialis
Louzao, M. C., Vieytes, M. R., Alfonso, A., & Botana, L. M. (1993) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(93)90015-v · Cited by 2
Effects of Protein Kinase C on the Na+-H+ Exchange in the Cochlear Outer Hair Cell
Ikeda, K., Sunose, H., & Takasaka, T. (1996) · Acta Oto-Laryngologica · doi:10.3109/00016489609137934 · Cited by 2
Gaudry-Talarmain, Y. M. (1984) · Neurochemistry International · doi:10.1016/0197-0186(84)90128-1 · Cited by 1
Intracellular Ca2+ does not activate the SITS-sensitive anion transporter in barnacle muscle
Matsumoto, P. S., & Russell, J. M. (1988) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/0005-2736(88)90172-1
Self-citationStudies on vascular intracellular pH in hypertension
Izzard, A. S. (1990) · OpenGrey (Institut de l'Information Scientifique et Technique)
Kraut, J. (2009) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1254971.722070
Putnam, R. W., & Roos, A. (1996) · Comprehensive physiology · doi:10.1002/j.2040-4603.1996.tb01759.x · Cited by 1
Ion Transport Across Mammalian Small Intestine
Sullivan, S. K., & Field, M. (1991) · Comprehensive physiology · doi:10.1002/j.2040-4603.1991.tb01408.x
Reddy, V. R. (2010) · theses.fr (ABES) · doi:10.70675/41bbee51zf096z43f5zad30za06a6786c5f1
Thornell, I. M., Michenkova, M., Taki, S., Bevensee, M. O., & Boron, W. F. (2026) · Elsevier eBooks · doi:10.1016/b978-0-12-815389-5.00077-0
Self-citationBoron, W. F. (1984) · Current topics in membranes and transport · doi:10.1016/s0070-2161(08)60473-6
Self-citation(1989) · PubMed · Cited by 1,639
Metadata
- Authors
- Boron, W. F., & Russell, J. M.
- ORCID
- Boron, W F
- Venue
- The Journal of general physiology
- Publisher
- Rockefeller University Press
- Published
- 1983-03-01
- Volume
- 81
- Issue
- 3
- Pages
- 373-399
- ISSN
- 0022-1295 (ISSN-L)
- 1540-7748
- PMC
- PMC2215574
- OpenAlex
- W2163004322
- Cited by
- 169
- References
- 15
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 1 · 2020: 2 · 2018: 1 · 2016: 1 · 2015: 1 · 2013: 2 · 2012: 1
- FWCI
- 6.52
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of General Physiology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › ATP Synthase and ATPases Research
- Keywords
- intracellular pH regulation, squid giant axon, acid extrusion, bicarbonate transport, sodium transport, chloride transport, satellite image time series, ATP dependence, Michaelis-Menten kinetics, acid load, pH-sensitive microelectrodes
- MeSH terms
- Acids, Animals, Bicarbonates, Biomechanical Phenomena, Chemistry, Chlorides, Hydrogen-Ion Concentration, Intracellular Membranes, Ions, Mathematics, Membrane Potentials, Models, Biological, Sodium, Decapodiformes, Chemical Phenomena
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review