Abstract
In this work we have investigated whether the asymmetrical properties of the Na/Ca exchange process found in intact preparations are intrinsic to the exchange protein(s) or the result of the asymmetric ionic environment normally prevailing in living cells. The activation of the Na/Ca exchanger by Ca2+ ions, monovalent cations, ATP gamma S and the effect of membrane potential on the different operational modes of the exchanger (Nao/Cai, Cao/Nai, Cao/Cai, and Nao/Nai) was studied in voltage-clamped squid giant axons externally perfused and internally dialyzed with symmetrical ionic solutions. Under these conditions: (a) Ca ions activate with higher affinity from the inside (K1/2 = 22 microM) than from the outside (K1/2 = 300 microM); (b) experiments measuring the Cao-dependent Ca efflux in the conditions Lio-Trisi, Lio- Lii, Triso-Trisi, and Triso-Lii, show that the activating monovalent cation site on the exchanger faces the external surface; (c) ATP gamma S activates the Cao-dependent Ca efflux (Cao/Cai exchange) only at nonsaturating [Ca2+]i. Its effect appears to be on the Ca transport site since no alteration in the apparent affinity of the activating monovalent cation site was observed. The above results show that the Na/Ca exchange process is indeed a highly asymmetric transport mechanism. Finally, the voltage dependence of the components of the different exchange modes was measured over the range of +20 to -40 mV. The voltage dependence (approximately 26% change/25 mV) was found to be similar for all modes of operation of the exchanger except Nao/Nai exchange, which was found to be voltage insensitive. The sensitivity of the Cao/Cai exchange to voltage was found to be the same in the presence and in the complete absence of monovalent cations. This finding does not support the proposition that the voltage sensitivity of the Cao/Cao exchange is induced by the binding and transport of an external monovalent cation.
Full Text
The Full Text of this article is available as a PDF (940.2 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allen T. J., Baker P. F. Comparison of the effects of potassium and membrane potential on the calcium-dependent sodium efflux in squid axons. J Physiol. 1986 Sep;378:53–76. doi: 10.1113/jphysiol.1986.sp016207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Allen T. J., Baker P. F. Influence of membrane potential on calcium efflux from giant axons of Loligo. J Physiol. 1986 Sep;378:77–96. doi: 10.1113/jphysiol.1986.sp016208. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baker P. F., Glitsch H. G. Does metabolic energy participate directly in the Na+-dependent extrusion of Ca2+ -Ca2+ ions from squid giant axons? J Physiol. 1973 Aug;233(1):44P–46P. [PubMed] [Google Scholar]
- Baker P. F., McNaughton P. A. Kinetics and energetics of calcium efflux from intact squid giant axons. J Physiol. 1976 Jul;259(1):103–144. doi: 10.1113/jphysiol.1976.sp011457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baker P. F. The regulation of intracellular calcium in giant axons of Loligo and Myxicola. Ann N Y Acad Sci. 1978 Apr 28;307:250–268. doi: 10.1111/j.1749-6632.1978.tb41956.x. [DOI] [PubMed] [Google Scholar]
- Bezanilla F., Caputo C., DiPolo R., Rojas H. Potassium conductance of the squid giant axon is modulated by ATP. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2743–2745. doi: 10.1073/pnas.83.8.2743. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blaustein M. P., Russell J. M., Weer P. Calcium efflux from internally dialyzed squid axons: the influence of external and internal cations. J Supramol Struct. 1974;2(5-6):558–581. doi: 10.1002/jss.400020505. [DOI] [PubMed] [Google Scholar]
- Blaustein M. P., Santiago E. M. Effects of internal and external cations and of ATP on sodium-calcium and calcium-calcium exchange in squid axons. Biophys J. 1977 Oct;20(1):79–111. doi: 10.1016/S0006-3495(77)85538-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blaustein M. P. The energetics and kinetics of sodium-calcium exchange in barnacle muscles, squid axons, and mammalian heart: the role of ATP. Soc Gen Physiol Ser. 1984;38:129–147. [PubMed] [Google Scholar]
- Caroni P., Carafoli E. The regulation of the Na+ -Ca2+ exchanger of heart sarcolemma. Eur J Biochem. 1983 May 16;132(3):451–460. doi: 10.1111/j.1432-1033.1983.tb07383.x. [DOI] [PubMed] [Google Scholar]
- DiPolo R., Beaugé L. Ca2+ transport in nerve fibers. Biochim Biophys Acta. 1988 Oct 11;947(3):549–569. doi: 10.1016/0304-4157(88)90007-x. [DOI] [PubMed] [Google Scholar]
- DiPolo R., Beaugé L. Characterization of the reverse Na/Ca exchange in squid axons and its modulation by Cai and ATP. Cai-dependent Nai/Cao and Nai/Nao exchange modes. J Gen Physiol. 1987 Oct;90(4):505–525. doi: 10.1085/jgp.90.4.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DiPolo R., Beaugé L. In squid axons, ATP modulates Na+-Ca2+ exchange by a Ca2+i-dependent phosphorylation. Biochim Biophys Acta. 1987 Mar 12;897(3):347–354. doi: 10.1016/0005-2736(87)90432-9. [DOI] [PubMed] [Google Scholar]
- DiPolo R., Beaugé L. Physiological role of ATP-driven calcium pump in squid axon. Nature. 1979 Mar 15;278(5701):271–273. doi: 10.1038/278271a0. [DOI] [PubMed] [Google Scholar]
- DiPolo R. Characterization of the ATP-dependent calcium efflux in dialyzed squid giant axons. J Gen Physiol. 1977 Jun;69(6):795–813. doi: 10.1085/jgp.69.6.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DiPolo R., Rojas H. Effect of internal and external K+ on Na+-Ca2+ exchange in dialyzed squid axons under voltage clamp conditions. Biochim Biophys Acta. 1984 Oct 3;776(2):313–316. doi: 10.1016/0005-2736(84)90220-7. [DOI] [PubMed] [Google Scholar]
- Dipolo R., Bezanilla F., Caputo C., Rojas H. Voltage dependence of the Na/Ca exchange in voltage-clamped, dialyzed squid axons. Na-dependent Ca efflux. J Gen Physiol. 1985 Oct;86(4):457–478. doi: 10.1085/jgp.86.4.457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dipolo R. Effect of ATP on the calcium efflux in dialyzed squid giant axons. J Gen Physiol. 1974 Oct;64(4):503–517. doi: 10.1085/jgp.64.4.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dipolo R., Requena J., Brinley F. J., Jr, Mullins L. J., Scarpa A., Tiffert T. Ionized calcium concentrations in squid axons. J Gen Physiol. 1976 Apr;67(4):433–467. doi: 10.1085/jgp.67.4.433. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mullins L. J., Brinley F. J., Jr Some factors influencing sodium extrusion by internally dialyzed squid axons. J Gen Physiol. 1967 Nov;50(10):2333–2355. doi: 10.1085/jgp.50.10.2333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Philipson K. D., Frank J. S., Nishimoto A. Y. Effects of phospholipase C on the Na+-Ca2+ exchange and Ca2+ permeability of cardiac sarcolemmal vesicles. J Biol Chem. 1983 May 10;258(9):5905–5910. [PubMed] [Google Scholar]
- Philipson K. D., Nishimoto A. Y. Efflux of Ca2+ from cardiac sarcolemmal vesicles. Influence of external Ca2+ and Na+. J Biol Chem. 1981 Apr 25;256(8):3698–3702. [PubMed] [Google Scholar]
- Philipson K. D., Nishimoto A. Y. Na+-Ca2+ exchange in inside-out cardiac sarcolemmal vesicles. J Biol Chem. 1982 May 10;257(9):5111–5117. [PubMed] [Google Scholar]
- Rasgado-Flores H., Blaustein M. P. Na/Ca exchange in barnacle muscle cells has a stoichiometry of 3 Na+/1 Ca2+. Am J Physiol. 1987 May;252(5 Pt 1):C499–C504. doi: 10.1152/ajpcell.1987.252.5.C499. [DOI] [PubMed] [Google Scholar]
- Slaughter R. S., Sutko J. L., Reeves J. P. Equilibrium calcium-calcium exchange in cardiac sarcolemmal vesicles. J Biol Chem. 1983 Mar 10;258(5):3183–3190. [PubMed] [Google Scholar]
- Wakabayashi S., Goshima K. Comparison of kinetic characteristics of Na+-Ca2+ exchange in sarcolemma vesicles and cultured cells from chick heart. Biochim Biophys Acta. 1981 Jul 20;645(2):311–317. doi: 10.1016/0005-2736(81)90202-9. [DOI] [PubMed] [Google Scholar]