Cell junction and cyclic AMP

III. Promotion of junctional membrane permeability and junctional membrane particles in a junction-deficient cell type

R. Azarnia, Gerhard Dahl, W. R. Loewenstein

Research output: Contribution to journalArticle

81 Citations (Scopus)

Abstract

The cyclic nucleotide effect on junction was studied in C1-1D cells, a mouse cancer cell type that fails to make permeable junctions in ordinary confluent culture. Upon administration of cyclic AMP, dibutyryl cyclic AMP, dibutyryl cyclic AMP plus caffeine (db-cAMP-caffeine), or cholera toxin (an adenylate cyclase activator), the cells acquired permeable junctions; they became electrically coupled and transferred fluorescent tracer molecules among each other-a transfer exhibiting the molecular size limit of permeation of normal cell-to-cell channels. The effect took several hours to develop. With the db-cAMP-caffeine treatment, junctional permeability emerged within two hours in one-fifth of the cell opopulation, and within the next few hours in the entire population. This development was not prevented by the cytokinesis inhibitor cytochalasin B. Permeable junctions formed also in two other conditions where the cell-endogenous cyclic AMP level may be expected to increase: serum starvation and low cell density. After three weeks of starving the cells of serum, a junctional permeability arose in confluent cultures, which on feeding with serum disappeared within two to three days. At low cell density, namely below confluency, the cells made permeable junctions, unstarved. In cultures of rather uniform density, the frequency of permeable junctions was inversely related to the average density, over the subconfluent range; at densities of about 1×104 cells/cm2, where the cells had few mutual contacts, 80% of the pairs presumed to be in contact were electrically coupled. In cultures with adjoining territories of high (confluent) and low cell density, there was coupling only in the last, and in this low-density state the cells were also capable of coupling with other mammalian cell types (mouse 3T3-BalbC and human Lesch-Nyhan cells). Correlated electron microscopy of freeze-fractured cell junctions showed no membrane differentiation in confluent C1-1D cultures. The junctions acquired differentiations, namely particle clusters of gap junction and strands of tight junction, upon cyclic nucleotide application or serum starvation and in the lowdensity condition. With db-cAMP-caffeine, these differentiations appeared within 4 hr of the treatment (confluent cultures), growing in size over the next hours. Treatment with cycloheximide, but not with cytochalasin B, prevented the development of recognizable gap junction and tight junction in cultures supplied with db-cAMP-caffeine.

Original languageEnglish
Pages (from-to)133-146
Number of pages14
JournalThe Journal of Membrane Biology
Volume63
Issue number1-2
DOIs
StatePublished - Oct 1 1981

Fingerprint

Intercellular Junctions
Cyclic AMP
Permeability
Membranes
Bucladesine
Caffeine
Cell Count
Cytochalasin B
Tight Junctions
Gap Junctions
Cyclic Nucleotides
Starvation
Serum
3T3 Cells
Cytokinesis
Cholera Toxin
Cycloheximide
Adenylyl Cyclases
Electron Microscopy

Keywords

  • cancer cell
  • cell junction
  • cell-to-cell membrane channels
  • cyclic AMP
  • gap junction
  • Intercellular communication
  • junctional permeability
  • membrane permeability
  • promotion of cell-to-cell membrane channels

ASJC Scopus subject areas

  • Physiology
  • Cell Biology
  • Biophysics

Cite this

Cell junction and cyclic AMP : III. Promotion of junctional membrane permeability and junctional membrane particles in a junction-deficient cell type. / Azarnia, R.; Dahl, Gerhard; Loewenstein, W. R.

In: The Journal of Membrane Biology, Vol. 63, No. 1-2, 01.10.1981, p. 133-146.

Research output: Contribution to journalArticle

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