Home LiteratureArticle Details
PMID: 24172983 Published · ppublish English Journal Article

Junctional membrane permeability : Depression by substitution of Li for extracellular Na, and by long-term lack of Ca and Mg; restoration by cell repolarization.

The Journal of membrane biology ·Vol. 5 ·No. 1 ·1971-03-00 ·Pages 20-50

Rose B, Loewenstein WR

Abstract

Substitution of extracellular Na(+) by Li(+) causes depression of junctional membrane permeability inChironomus salivary gland cells; within 3 hr, permeability falls to so low a level that neither fluorescein nor the smaller inorganic ions any longer traverse the junctional membrane in detectable amounts (uncoupling). The effect is Li-specific: if choline(+) is the Na(+) substitute, coupling is unchanged. The Li-produced uncoupling is not reversed by restitution of Na(+). Long-term exposure (>1 hr) of the cells to Ca, Mg-free medium leads also to uncoupling. This uncoupling is fully reversible by early restitution of Ca(++) or Mg(++). Coupling is maintained in the presence of either Ca(++) or Mg(++), so long as the total divalent concentration is about 12MM. The uncoupling in Ca, Mg-free medium ensues regardless of whether the main monovalent cation is Na, Li or choline.The uncouplings are accompanied by cell depolarization. Repolarization of the cells by inward current causes restoration of coupling; the junctional conductance rises again to its normal level. The effect was shown for Li-produced uncoupling, for uncoupling by prolonged absence of external Ca(++) and Mg(++), and for uncoupling produced by dinitrophenol. In all cases, the recoupling has the same features: (1) it develops rapidly upon application of the polarizing current; (2) it is cumulative; (3) it is transient, but outlasts the current; and (4) it appears not to depend on the particular ions carrying the current from the electrodes to the cell. The recoupling is due to repolarization of nonjunctional cell membrane; recoupling can be produced at zero net currernt through the junctional membrane. Recoupling takes place also as a result of chemically produced repolarization; restoration of theK gradients in uncoupled cells causes partial recoupling during the repolarization phase.An explanation of the results on coupling is proposed in terms of known mechanisms of regulation of Ca(++) flux in cells. The uncouplings are explained by actions raising the Ca(++) level in the cytoplasmic environment of the junctional membranes; the recoupling is explained by actions lowering this Ca(++) level.

Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rose B
Cell Physics Laboratory, Department of Physiology, Columbia University College of Physicians & Surgeons, 10032, New York, New York.
Loewenstein W R
References (47)
47 references, click to expand
  1. THE DEPENDENCE OF CONTRACTION AND RELAXATION OF MUSCLE FIBRES FROM THE CRAB MAIA SQUINADO ON THE INTERNAL CONCENTRATION OF FREE CALCIUM IONS.
    Biochim Biophys Acta. 1964 May 25;79:581-91 PMID: 14179458
  2. [Uptake and release of calcium in erythrocytes in man].
    Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1962;244:172-84 PMID: 13975527
  3. Crayfish muscle: permeability to sodium induced by calcium depletion.
    Science. 1967 Mar 10;155(3767):1263-6 PMID: 4959889
  4. Intercellular communication and some structural aspects of membrane junctions in a simple cell system.
    J Membr Biol. 1971 Mar;5(1):1-19 PMID: 24172982
  5. In vitro studies of the gain and exchange of calcium in frog skeletal muscle.
    J Gen Physiol. 1961 Jul;44:1121-30 PMID: 13695749
  6. The calcium content of the smooth muscle of the guinea-pig taenia coli.
    J Physiol. 1967 Sep;192(1):145-57 PMID: 6051800
  7. THE STEADY STATE MAINTENANCE OF ACCUMULATED CA++ IN RAT LIVER MITOCHONDRIA.
    J Biol Chem. 1965 Jun;240:2712-20 PMID: 14304890
  8. Stimulation of 45Ca efflux from smooth muscle by extracellular Ca2+.
    Biochim Biophys Acta. 1968 Aug;163(1):114-6 PMID: 5673938
  9. Calcium distribution and exchange in the rat uterus.
    J Gen Physiol. 1966 Jul;49(6):1265-97 PMID: 5924111
  10. Cell-to-cell passage of large molecules.
    Nature. 1966 Nov 5;212(5062):629-30 PMID: 5971695
  11. THE BIOCHEMISTRY OF SODIUM TRANSPORT.
    Biol Rev Camb Philos Soc. 1964 May;39:160-93 PMID: 14163535
  12. Sodium-dependent uptake of calcium by crab nerve.
    Biochim Biophys Acta. 1968 Jan 3;150(1):167-70 PMID: 5642631
  13. A comparative study of the role of mitochondria and the sarcoplasmic reticulum in the uptake and release of Ca++ by the rat diaphragm.
    J Cell Physiol. 1969 Aug;74(1):17-30 PMID: 5799499
  14. Calcium uptake in mitochondria and vesicles of heart and skeletal muscle in presence of potassium, sodium, k-strophanthin and pentobarbital.
    Biochem Pharmacol. 1969 Jun;18(6):1335-45 PMID: 5799107
  15. Surface density of calcium ions and calcium spikes in the barnacle muscle fiber membrane.
    J Gen Physiol. 1967 Jan;50(3):583-601 PMID: 11526848
  16. Junctional membrane permeability: restoration by repolarizing current.
    Science. 1970 Aug 7;169(3945):607-9 PMID: 4987682
  17. The dependence of calcium efflux from cardiac muscle on temperature and external ion composition.
    J Physiol. 1968 Mar;195(2):451-70 PMID: 5647333
  18. Rapid, respiration-independent binding of alkali metal cations by rat liver mitochondria.
    J Biol Chem. 1968 Jul 25;243(14):3953-62 PMID: 5661718
  19. Biology and pharmacology of the lithium ion.
    Pharmacol Rev. 1957 Mar;9(1):17-58 PMID: 13431415
  20. ATP-dependent Ca++-extrusion from human red cells.
    Experientia. 1966 Jun 15;22(6):364-5 PMID: 5961668
  21. Two phases of calcium entry during the action potential in giant axons of Loligo.
    J Physiol. 1970 Jun;208(2):80P-82P PMID: 5500759
  22. The influence of high potassium depolarization and acetylcholine on calcium exchange in the rat uterus.
    J Gen Physiol. 1966 Jul;49(6):1299-317 PMID: 5924112
  23. On the genesis of cellular communication.
    Dev Biol. 1967 Jun;15(6):503-20 PMID: 6033174
  24. RESTORATION OF ACTION POTENTIAL BY ANODAL POLARIZATION IN LOBSTER GIANT AXONS.
    J Cell Comp Physiol. 1964 Aug;64:73-96 PMID: 14200353
  25. Permeability of a cell membrane junction. Dependence on energy metabolism.
    J Gen Physiol. 1969 Apr;53(4):498-515 PMID: 5778320
  26. Effects of lithium on different membrane components of crayfish stretch receptor neurons.
    J Gen Physiol. 1968 May;51(5):635-54 PMID: 5654404
  27. The dual effect of calcium on the action potential of the frog's heart.
    J Physiol. 1966 May;184(2):291-311 PMID: 5921832
  28. Wilhelm Roux Arch Entwickl Mech Org. 1940 Jun;140(2):168-194 PMID: 28354005
  29. Action of external divalent ion reduction on sodium movement in the squid giant axon.
    J Gen Physiol. 1961 Sep;45:93-103 PMID: 13681454
  30. Aspects of the relationship between membrane potential, calcium transient and tension in single barnacle muscle fibres.
    J Physiol. 1969 Jan;200(1):74P-6P PMID: 5761992
  31. Cell surface membranes in close contact. Role of calcium and magnesium ions.
    J Colloid Interface Sci. 1967 Sep;25(1):34-46 PMID: 6080826
  32. Junctional membrane permeability : Effects of divalent cations.
    J Membr Biol. 1971 Mar;5(1):51-77 PMID: 24172984
  33. The permeability of frog muscle fibres to lithium ions.
    J Physiol. 1959 Oct;147:626-38 PMID: 14408743
  34. Uncoupling cell junctions in a glandular epithelium by depolarizing current.
    Science. 1971 Apr 30;172(3982):492-4 PMID: 5550507
  35. The ultrastructure of frog ventricular cardiac muscle and its relationship to mechanism of excitation-contraction coupling.
    J Cell Biol. 1968 Jul;38(1):99-114 PMID: 5691981
  36. CALCIUM AND MAGNESIUM BINDING PROPERTIES OF CELL MEMBRANE MATERIALS.
    J Cell Comp Physiol. 1963 Dec;62:311-7 PMID: 14086154
  37. Permeability and structure of junctional membranes at an electrotonic synapse.
    Science. 1969 Dec 26;166(3913):1641-3 PMID: 5360587
  38. Calcium ions and the permeability of human erythrocytes.
    J Physiol. 1959 Dec;149:563-85 PMID: 13802308
  39. Active transport of cations in giant axons from Sepia and Loligo.
    J Physiol. 1955 Apr 28;128(1):28-60 PMID: 14368574
  40. Junctional membrane uncoupling. Permeability transformations at a cell membrane junction.
    J Gen Physiol. 1967 Aug;50(7):1865-91 PMID: 6050971
  41. Permeability of the giant axon of Dosidicus gigas to calcium ions.
    J Gen Physiol. 1968 May;51(5):Suppl:115S+ PMID: 5659020
  42. The action of calcium on the electrical properties of squid axons.
    J Physiol. 1957 Jul 11;137(2):218-44 PMID: 13449874
  43. Permeability of membrane junctions.
    Ann N Y Acad Sci. 1966 Jul 14;137(2):441-72 PMID: 5229810
  44. INFLUENCE OF LITHIUM IONS ON THE TRANSMEMBRANE POTENTIAL AND CATION CONTENT OF CARDIAC CELLS.
    J Gen Physiol. 1964 Jan;47:501-30 PMID: 14100967
  45. Depression of junctional membrane permeability by substitution of lithium for extracellular sodium.
    Biochim Biophys Acta. 1969 Jan 28;173(1):146-8 PMID: 5775937
  46. MOVEMENTS OF CA IN FROG HEART VENTRICLES AT REST AND DURING CONTRACTURES.
    J Physiol. 1963 Jul;167:515-50 PMID: 14178833
  47. EFFECT OF CALCIUM ON INTRACELLULAR SODIUM AND POTASSIUM CONCENTRATIONS IN PLANT AND ANIMAL CELLS.
    Nature. 1964 Nov 14;204:641-2 PMID: 14236276
Article Info
Journal
The Journal of membrane biology
Abbr.
J Membr Biol
ISSN
0022-2631
Published
1971-03-00
Pages
20-50
Language
English
Region
United States
NLM ID
0211301
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]