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. 1983 Nov 1;97(5):1459–1466. doi: 10.1083/jcb.97.5.1459

Calcium-mediated changes in gap junction structure: evidence from the low angle X-ray pattern

PMCID: PMC2112697  PMID: 6630291

Abstract

Rat liver gap junctions were isolated in Ca2+-free media and analyzed in controlled environments by x-ray diffraction of partially oriented pellets. Different treatments of the same preparations were compared. The ordered hexagonal lattices gave rise to detail that was sensitive to low Ca2+ concentrations (0.05 mM), but not to Mg2+ (up to 0.16 mM) or pH (between 6.0 and 8.0). The major Ca2+-mediated responses were reductions in the intensity of the (1, 0) peak and in the off- equatorial contributions to the (2, 1) peak, and changes of scale equivalent to a decrease (approximately 2%) in lattice dimension, but an increase (approximately 4%) in the dimension perpendicular to the lattice. A simple structural interpretation of these findings is that Ca2+ induces the subunits of the channel-forming assembly, the connexon, to align more nearly parallel to the channel, thereby causing the connexon to become slightly longer and more radially compact. The rearrangement is of the same nature as one found under less physiological circumstances by electron microscopy (Unwin, P. N. T., and G. Zampighi, 1980, Nature (Lond.)., 283:545-549), and may be part of a coordinated mechanism by which the channel closes.

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Selected References

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

  1. Caspar D. L., Goodenough D. A., Makowski L., Phillips W. C. Gap junction structures. I. Correlated electron microscopy and x-ray diffraction. J Cell Biol. 1977 Aug;74(2):605–628. doi: 10.1083/jcb.74.2.605. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Goodenough D. A. In vitro formation of gap junction vesicles. J Cell Biol. 1976 Feb;68(2):220–231. doi: 10.1083/jcb.68.2.220. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Harris A. L., Spray D. C., Bennett M. V. Kinetic properties of a voltage-dependent junctional conductance. J Gen Physiol. 1981 Jan;77(1):95–117. doi: 10.1085/jgp.77.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hertzberg E. L., Lawrence T. S., Gilula N. B. Gap junctional communication. Annu Rev Physiol. 1981;43:479–491. doi: 10.1146/annurev.ph.43.030181.002403. [DOI] [PubMed] [Google Scholar]
  5. Johnston M. F., Ramón F. Electrotonic coupling in internally perfused crayfish segmented axons. J Physiol. 1981 Aug;317:509–518. doi: 10.1113/jphysiol.1981.sp013840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Loewenstein W. R. Junctional intercellular communication: the cell-to-cell membrane channel. Physiol Rev. 1981 Oct;61(4):829–913. doi: 10.1152/physrev.1981.61.4.829. [DOI] [PubMed] [Google Scholar]
  7. Makowski L., Caspar D. L., Goodenough D. A., Phillips W. C. Gap Junction Structures: III. The Effect of Variations in the Isolation Procedure. Biophys J. 1982 Jan;37(1):189–191. doi: 10.1016/S0006-3495(82)84663-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Makowski L., Caspar D. L., Phillips W. C., Goodenough D. A. Gap junction structures. II. Analysis of the x-ray diffraction data. J Cell Biol. 1977 Aug;74(2):629–645. doi: 10.1083/jcb.74.2.629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Obaid A. L., Socolar S. J., Rose B. Cell-to-cell channels with two independently regulated gates in series: analysis of junctional conductance modulation by membrane potential, calcium, and pH. J Membr Biol. 1983;73(1):69–89. doi: 10.1007/BF01870342. [DOI] [PubMed] [Google Scholar]
  10. Rose B., Loewenstein W. R. Permeability of cell junction depends on local cytoplasmic calcium activity. Nature. 1975 Mar 20;254(5497):250–252. doi: 10.1038/254250a0. [DOI] [PubMed] [Google Scholar]
  11. Spray D. C., Stern J. H., Harris A. L., Bennett M. V. Gap junctional conductance: comparison of sensitivities to H and Ca ions. Proc Natl Acad Sci U S A. 1982 Jan;79(2):441–445. doi: 10.1073/pnas.79.2.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Thomas M. V., Gorman A. L. Internal calcium changes in a bursting pacemaker neuron measured with arsenazo III. Science. 1977 Apr 29;196(4289):531–533. doi: 10.1126/science.850795. [DOI] [PubMed] [Google Scholar]
  13. Turin L., Warner A. E. Intracellular pH in early Xenopus embryos: its effect on current flow between blastomeres. J Physiol. 1980 Mar;300:489–504. doi: 10.1113/jphysiol.1980.sp013174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Unwin P. N., Zampighi G. Structure of the junction between communicating cells. Nature. 1980 Feb 7;283(5747):545–549. doi: 10.1038/283545a0. [DOI] [PubMed] [Google Scholar]
  15. Zampighi G., Unwin P. N. Two forms of isolated gap junctions. J Mol Biol. 1979 Dec 5;135(2):451–464. doi: 10.1016/0022-2836(79)90446-7. [DOI] [PubMed] [Google Scholar]

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