Literature DB >> 3722262

Electrophysiological properties of gap junctions between dissociated pairs of rat hepatocytes.

D C Spray, R D Ginzberg, E A Morales, Z Gatmaitan, I M Arias.   

Abstract

Physiological properties of isolated pairs of rat hepatocytes were examined within 5 h after dissociation. These cells become round when separated, but cell pairs still display membrane specializations. Most notably, canaliculi are often present at appositional membranes which are flanked by abundant gap and tight junctions. These cell pairs are strongly dye-coupled; Lucifer Yellow CH injected into one cell rapidly diffuses to the other. Pairs of hepatocytes are closely coupled electrically. Conductance of the junctional membrane is not voltage sensitive: voltage clamp studies demonstrate that gj is constant in response to long (5 s) transjunctional voltage steps of either polarity (to greater than +/- 40 mV from rest). Junctional conductance (gj) between hepatocyte pairs is reduced by exposure to octanol (0.1 mM) and by intracellular acidification. Normal intracellular pH (pHi), measured with a liquid ion exchange microelectrode, was generally 7.1-7.4, and superfusion with saline equilibrated with 100% CO2 reduced pHi to 6.0-6.5. In the pHi range 7.5-6.6, gj was constant. Below pH 6.6, gj steeply decreased and at 6.1 coupling was undetectable. pHi recovered when cells were rinsed with normal saline; in most cases gj recovered in parallel so that gj values were similar for pHs obtained during acidification or recovery. The low apparent pK and very steep pHi-gj relation of the liver gap junction contrast with higher pKs and more gradually rising curves in other tissues. If H+ ions act directly on the junctional molecules, the channels that are presumably homologous in different tissues must differ with respect to reactive sites or their environment.

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Year:  1986        PMID: 3722262      PMCID: PMC2113793          DOI: 10.1083/jcb.103.1.135

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


  33 in total

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Journal:  Nature       Date:  1975-03-20       Impact factor: 49.962

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Journal:  Nature       Date:  1980-02-07       Impact factor: 49.962

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Journal:  J Cell Biol       Date:  1978-08       Impact factor: 10.539

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Journal:  J Cell Biol       Date:  1966-04       Impact factor: 10.539

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Journal:  J Cell Biol       Date:  1969-12       Impact factor: 10.539

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  30 in total

1.  Membrane modifications in the course of hepatocyte isolation.

Authors:  E Falcieri; R Del Coco; A R Mariani; P Gobbi; P Santi
Journal:  Cytotechnology       Date:  1990-11       Impact factor: 2.058

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Authors:  S C McKarns; D J Doolittle
Journal:  Cell Biol Toxicol       Date:  1992 Jan-Mar       Impact factor: 6.691

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Journal:  Biophys J       Date:  1991-04       Impact factor: 4.033

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Authors:  A P Moreno; B Eghbali; D C Spray
Journal:  Biophys J       Date:  1991-11       Impact factor: 4.033

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Authors:  T Tordjmann; B Berthon; M Claret; L Combettes
Journal:  EMBO J       Date:  1997-09-01       Impact factor: 11.598

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Authors:  B Eghbali; J A Kessler; D C Spray
Journal:  Proc Natl Acad Sci U S A       Date:  1990-02       Impact factor: 11.205

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Journal:  J Membr Biol       Date:  1989-11       Impact factor: 1.843

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Authors:  Jorge E Contreras; Helmuth A Sánchez; Loreto P Véliz; Feliksas F Bukauskas; Michael V L Bennett; Juan C Sáez
Journal:  Brain Res Brain Res Rev       Date:  2004-12

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Authors:  J C Wilton; J K Chipman; C J Lawson; A J Strain; R Coleman
Journal:  Biochem J       Date:  1993-06-15       Impact factor: 3.857

10.  Hemi-gap-junction channels in solitary horizontal cells of the catfish retina.

Authors:  S H DeVries; E A Schwartz
Journal:  J Physiol       Date:  1992-01       Impact factor: 5.182

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