Literature DB >> 10605455

Quantitative analysis of low-resistance junctions between cultured cells and correlation with gap-junctional areas.

J D Sheridan1, M Hammer-Wilson, D Preus, R G Johnson.   

Abstract

Electrophysiological studies of low-resistance junctions between Novikoff hepatoma cells grown in suspension cultures were carried out and correlated with gap-junctional areas per inferface determined by freeze-fracture. The mean coupling coefficient between isolated cell pairs was 0.773 +/- 0.025 (SEM) in 67G medium and 0.653 +/- 0.028 in M67 medium; the respective means for the central pairs of four-cell chains were 0.714 +/- 0.034 and 0.595 +/- 0.026. Mean estimates of nonjunctional resistances for cell pairs were 3.0 +/- 0.32 x 10(7) ohm (67G) and 2.01 +/- 0.01 x 10(7) ohm (M67), and the respective estimates for specific nonjunctional resistances were 158.6 +/- 8.1 ohm-cm2 (67G) and 133.0 +/- 812 ohm-cm2 (M67). Mean estimates of junctional conductances were 0.409 +/- 0.058 x 10(-6) mho (67G) and 0.211 +/- 0.018 x 10(-6) mho (M67) for pairs and 0.291 +/- 0.063 x 10(-6) mho (67G) and 0.212 +/- 0.04 mho (M67) for four-cell chains. The mean area of gap junction per interface for separate cell populations was 0.187 +/- 0.049 micron 2 and 0.269 +/- 0.054 micron 2 for cells fixed in loose pellets and in suspension, respectively. When compared with the mean junctional conductance, these values gave specific junctional conductance estimates of 1.13 x 10(2) mho/cm2 and 0.78 x 10(2) mho/cm2, respectively. These values are higher than most previous estimates, but are consistent with the hypothesis that gap-junctional particles contain central hydrophilic channels, about 2 nm in diameter, which have cytoplasmic resistivity.

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Year:  1978        PMID: 10605455      PMCID: PMC2109986          DOI: 10.1083/jcb.76.2.532

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  20 in total

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Authors:  R G Johnson; J D Sheridan
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4.  Temperature-dependence of resistance at an electrotonic synapse.

Authors:  B W Payton; M V Bennett; G D Pappas
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5.  Physiology of electrotonic junctions.

Authors:  M V Bennett
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6.  Connections between cells of the developing squid as revealed by electrophysiological methods.

Authors:  D D Potter; E J Furshpan; E S Lennox
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7.  The nexus in the intercalated disc of the canine heart: quantitative data for an estimation of its resistance.

Authors:  A W Spira
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9.  Junctional membrane uncoupling. Permeability transformations at a cell membrane junction.

Authors:  W R Loewenstein; M Nakas; S J Socolar
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Authors:  H Subak-Sharpe; R R Bürk; J D Pitts
Journal:  J Cell Sci       Date:  1969-03       Impact factor: 5.285

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  15 in total

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Authors:  P R Benjamin; J B Pilkington
Journal:  J Physiol       Date:  1986-01       Impact factor: 5.182

3.  Development of electrical coupling and action potential synchrony between paired aggregates of embryonic heart cells.

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4.  Gap junctions in laryngeal carcinoma.

Authors:  P Schenk
Journal:  Arch Otorhinolaryngol       Date:  1980

5.  Cell-to-cell communication in monolayers of epithelioid cells (MDCK) as a function of the age of the monolayer.

Authors:  M Cereijido; E Robbins; D D Sabatini; E Stefani
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6.  Junctional transfer in cultured vascular endothelium: I. Electrical coupling.

Authors:  D M Larson; E Y Kam; J D Sheridan
Journal:  J Membr Biol       Date:  1983       Impact factor: 1.843

7.  Gap junctions and impulse propagation in embryonic epithelium of Amphibia. A freeze-etching study.

Authors:  M P Chuang-Tseng; H H Chuang; C Sandri; K Akert
Journal:  Cell Tissue Res       Date:  1982       Impact factor: 5.249

8.  Voltage independence of an electrotonic synapse.

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Review 9.  Lipids in gap junction assembly and function.

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Journal:  Lipids       Date:  1990-08       Impact factor: 1.880

10.  Gap junction remodeling associated with cholesterol redistribution during fiber cell maturation in the adult chicken lens.

Authors:  Sondip K Biswas; Jean X Jiang; Woo-Kuen Lo
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