Literature DB >> 7309793

Intercellular communication in normal and regenerating rat liver: a quantitative analysis.

D J Meyer, S B Yancey, J P Revel.   

Abstract

We have compared intercellular communication in the regenerating and normal livers of weanling rats. The electrophysiological studies were conducted at the edge of the liver, and we have found that here as elsewhere in the liver there is a dramatic decrease in the number and size of gap junctions during regeneration. The area of hepatocyte membrane occupied by gap junctions is reduced 100-fold 29-35 h after hepatectomy. By combining observations made with the scanning electron microscope with our freeze fracture data we have estimated the number of "communicating interfaces" (areas of contact between hepatocytes that include at least one gap junction) formed by hepatocytes in normal and regenerating liver. In normal liver a hepatocyte forms gap junctions with every hepatocyte it contacts (approximately 6). In regenerating liver a hepatocyte forms detectable gap junctions with, on average, only one other hepatocyte. Intercellular spread of fluorescent dye and electric current is reduced in regenerating as compared with normal liver. The incidence of electric coupling is reduced from 100% of hepatocyte pairs tested in control liver to 92% in regenerating liver. Analysis of the spatial dependence of electronic potentials indicates a substantial increase in intercellular resistance in regenerating liver. A quantitative comparison of our morphological and physiological data is complicated by tortuous pattern of current flow and by inhomogeneities in the liver during regeneration. Nevertheless we believe that our results are consistent with the hypothesis that gap junctions are aggregates of channels between cell interiors.

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Year:  1981        PMID: 7309793      PMCID: PMC2111978          DOI: 10.1083/jcb.91.2.505

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


  43 in total

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Journal:  Science       Date:  1971-01-29       Impact factor: 47.728

6.  Electrical coupling between embryonic cells by way of extracellular space and specialized junctions.

Authors:  M V Bennett; J P Trinkaus
Journal:  J Cell Biol       Date:  1970-03       Impact factor: 10.539

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8.  Intercellular communication and tissue growth. II. Tissue regeneration.

Authors:  W R Loewenstein; R D Penn
Journal:  J Cell Biol       Date:  1967-05       Impact factor: 10.539

9.  Correlated morphometric and biochemical studies on the liver cell. I. Morphometric model, stereologic methods, and normal morphometric data for rat liver.

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Journal:  J Cell Biol       Date:  1969-07       Impact factor: 10.539

10.  Electrical transmission at the nexus between smooth muscle cells.

Authors:  L Barr; W Berger; M M Dewey
Journal:  J Gen Physiol       Date:  1968-03       Impact factor: 4.086

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  36 in total

1.  Changes in electrical resistivity of swine liver after occlusion and postmortem.

Authors:  D Haemmerich; R Ozkan; S Tungjitkusolmun; J Z Tsai; D M Mahvi; S T Staelin; J G Webster
Journal:  Med Biol Eng Comput       Date:  2002-01       Impact factor: 2.602

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

Review 3.  Liver regeneration in relationship to acute liver failure.

Authors:  C D Gove; R D Hughes
Journal:  Gut       Date:  1991-09       Impact factor: 23.059

4.  Cell Volume Fluctuations in MDCK Monolayers.

Authors:  Steven M Zehnder; Melanie Suaris; Madisonclaire M Bellaire; Thomas E Angelini
Journal:  Biophys J       Date:  2015-01-20       Impact factor: 4.033

5.  Binding of 3H-phenamil, an irreversible amiloride analog, to toad urinary bladder: effects of aldosterone and vasopressin.

Authors:  J L Garvin; S A Simon; E J Cragoe; L J Mandel
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

6.  Haemodynamic and ultrastructural observations on the rat liver after two-thirds partial hepatectomy.

Authors:  E Morsiani; A Aleotti; D Ricci
Journal:  J Anat       Date:  1998-05       Impact factor: 2.610

7.  A structural analysis of gap and tight junctions in the rat liver during a dietary treatment that induces oval cell proliferation.

Authors:  L H Spelman; N L Thompson; N Fausto; K R Miller
Journal:  Am J Pathol       Date:  1986-11       Impact factor: 4.307

8.  Reduction of gap junction protein connexin 32 in rat atrophic gastric mucosa as an early event in carcinogenesis.

Authors:  A Nagahara; S Watanabe; H Miwa; K Endo; M Hirose; N Sato
Journal:  J Gastroenterol       Date:  1996-08       Impact factor: 7.527

9.  Degradation and resynthesis of gap junction protein in plasma membranes of regenerating liver after partial hepatectomy or cholestasis.

Authors:  O Traub; P M Drüge; K Willecke
Journal:  Proc Natl Acad Sci U S A       Date:  1983-02       Impact factor: 11.205

10.  Biochemical and genetic investigations on gap junctions from mammalian cells.

Authors:  K Willecke; R Dermietzel; P M Drüge; U Frixen; U Janssen-Timmen; R Schäfer; O Traub
Journal:  Biophys Struct Mech       Date:  1982
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