Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1973 Jul 1;58(1):1–10. doi: 10.1083/jcb.58.1.1

SELECTIVE DEPOSITION OF LANTHANUM IN MAMMALIAN CARDIAC CELL MEMBRANES

Ultrastructural and Electrophysiological Evidence

A Martinez-Palomo 1, D Benitez 1, J Alanis 1
PMCID: PMC2109026  PMID: 4125370

Abstract

Perfusion of beating false tendons of the dog heart with ionic lanthanum produced drastic but reversible modifications of the excitability and the transmembrane action potential of Purkinje cells. Ultrastructural examination of these cells revealed the appearance of a fine extracellular precipitate detectable on unstained sections. In addition, specimens perfused with La+++ showed a striking increase in the contrast of the sarcolemma, particularly in gap junctions and in pinocytic vesicles. La+++ deposits were restricted to the cytoplasmic leaflets of the sarcolemma; no precipitates were found at the plasma membrane of fibroblasts, endothelial and smooth muscle cells, or unmyelinated nerve fibers present in the same specimens. A selective deposition of La+++ was also observed in the sarcolemma of atrial and ventricular cells of dog, rabbit, and cat hearts, as well as in the membrane of the transverse tubular system of ventricular cells. Both the electrophysiological effects and the ultrastructural membrane deposits produced by La+++ disappeared when the specimens were subsequently perfused with phosphate-containing tyrode solution. These results tend to demonstrate that a distinctive feature of the sarcolemma of mammalian cardiac cells is the presence of regions with a high surface density of binding sites for polyvalent cations.

Full Text

The Full Text of this article is available as a PDF (857.5 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brady A. J., Woodbury J. W. The sodium-potassium hypothesis as the basis of electrical activity in frog ventricle. J Physiol. 1960 Dec;154(2):385–407. doi: 10.1113/jphysiol.1960.sp006586. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. CRANEFIELD P. F., EYSTER J. A. E., GILSON W. E. Effects of reduction of external sodium chloride on the injury potentials of cardiac muscle. Am J Physiol. 1951 Aug;166(2):269–272. doi: 10.1152/ajplegacy.1951.166.2.269. [DOI] [PubMed] [Google Scholar]
  3. DOGGENWEILER C. F., FRENK S. STAINING PROPERTIES OF LANTHANUM ON CELL MEMBRANES. Proc Natl Acad Sci U S A. 1965 Feb;53:425–430. doi: 10.1073/pnas.53.2.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Fawcett D. W., McNutt N. S. The ultrastructure of the cat myocardium. I. Ventricular papillary muscle. J Cell Biol. 1969 Jul;42(1):1–45. doi: 10.1083/jcb.42.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Heuser J., Miledi R. Effects of lanthanum ions on function and structure of frog neuromuscular junctions. Proc R Soc Lond B Biol Sci. 1971 Dec 14;179(1056):247–260. doi: 10.1098/rspb.1971.0096. [DOI] [PubMed] [Google Scholar]
  6. Khan T., Overton J. Staining of intercellular material in reaggregating chick liver and cartilage cells. J Exp Zool. 1969 Jun;171(2):161–173. doi: 10.1002/jez.1401710204. [DOI] [PubMed] [Google Scholar]
  7. LETTVIN J. Y., PICKARD W. F., MCCULLOCH W. S., PITTS W. A THEORY OF PASSIVE ION FLUX THROUGH AXON MEMBRANES. Nature. 1964 Jun 27;202:1338–1339. doi: 10.1038/2021338a0. [DOI] [PubMed] [Google Scholar]
  8. Langer G. A., Frank J. S. Lanthanum in heart cell culture. Effect on calcium exchange correlated with its localization. J Cell Biol. 1972 Sep;54(3):441–455. doi: 10.1083/jcb.54.3.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lesseps R. J. The removal by phospholipase C of a layer of lanthanum-staining material external to the cell membrane in embryonic chick cells. J Cell Biol. 1967 Jul;34(1):173–183. doi: 10.1083/jcb.34.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Machen T. E., Erlij D., Wooding F. B. Permeable junctional complexes. The movement of lanthanum across rabbit gallbladder and intestine. J Cell Biol. 1972 Aug;54(2):302–312. doi: 10.1083/jcb.54.2.302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Martinez-Palomo A., Erlij D., Bracho H. Localization of permeability barriers in the frog skin epithelium. J Cell Biol. 1971 Aug;50(2):277–287. doi: 10.1083/jcb.50.2.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Martínez-Palomo A. Ultrastructural modifications of intercellular junctions in some epithelial tumors. Lab Invest. 1970 Jun;22(6):605–614. [PubMed] [Google Scholar]
  13. McNutt N. S., Weinstein R. S. The ultrastructure of the nexus. A correlated thin-section and freeze-cleave study. J Cell Biol. 1970 Dec;47(3):666–688. doi: 10.1083/jcb.47.3.666. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Mines G. R. The action of beryllium, lanthanum, yttrium and cerium on the frog's heart. J Physiol. 1910 May 13;40(4):327–346. doi: 10.1113/jphysiol.1910.sp001373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Revel J. P., Karnovsky M. J. Hexagonal array of subunits in intercellular junctions of the mouse heart and liver. J Cell Biol. 1967 Jun;33(3):C7–C12. doi: 10.1083/jcb.33.3.c7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Sanborn W. G., Langer G. A. Specific uncoupling of excitation and contraction in mammalian cardiac tissue by lanthanum. J Gen Physiol. 1970 Aug;56(2):191–217. doi: 10.1085/jgp.56.2.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sanders E. J., Zalik S. E. Studies on the surface of chick blastoderm cells. II. Electron microscopy of surface binding characteristics. J Cell Physiol. 1972 Apr;79(2):235–248. doi: 10.1002/jcp.1040790208. [DOI] [PubMed] [Google Scholar]
  18. Shea S. M. Lanthanum staining of the surface coat of cells. Its enhancement by the use of fixatives containing Alcian blue or cetylpyridinium chloride. J Cell Biol. 1971 Dec;51(3):611–620. doi: 10.1083/jcb.51.3.611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Takata M., Pickard W. F., Lettvin J. Y., Moore J. W. Ionic conductance changes in lobster axon membrane when lanthanum is substituted for calcium. J Gen Physiol. 1966 Nov;50(2):461–471. doi: 10.1085/jgp.50.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES