Literature DB >> 2446941

Dieldrin inhibition of gap junctional intercellular communication in rat glial cells as measured by the fluorescence photobleaching and scrape loading/dye transfer assays.

S Suter1, J E Trosko, M H el-Fouly, L R Lockwood, A Koestner.   

Abstract

Application of the fluorescence-recovery after photobleaching (FRAP analysis) technique and scrape loading/dye transfer assay was made to measure the presence of gap junctional communication in primary rat glial cells in vitro in the presence and absence of the neurotoxicant and tumor promoter dieldrin, a chlorinated insecticide. Results demonstrate that primary rat glial cells are able to exhibit gap junctional intercellular communication and that dieldrin at noncytotoxic concentrations can modulate gap junctional communication as early as 10 min after exposure to the chemical and that the effect is reversible after 4 hr recovery from the dieldrin exposure. Both the FRAP analysis and the scrape loading/dye transfer assay have validated the observation that dieldrin inhibits gap junctional communication in other cell types using different techniques to measure gap junction function. These results were interpreted as an indication that inhibition of gap junctional communication might contribute to the cellular mechanism of dieldrin's neurotoxicity.

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Year:  1987        PMID: 2446941     DOI: 10.1016/0272-0590(87)90185-0

Source DB:  PubMed          Journal:  Fundam Appl Toxicol        ISSN: 0272-0590


  7 in total

1.  C-erbB2/neu transfection induces gap junctional communication incompetence in glial cells.

Authors:  A Hofer; J C Sáez; C C Chang; J E Trosko; D C Spray; R Dermietzel
Journal:  J Neurosci       Date:  1996-07-15       Impact factor: 6.167

2.  Limitations of the scrape-loading/dye transfer technique to quantify inhibition of gap junctional intercellular communication.

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

3.  Chemical requirements for inhibition of gap junction communication by the biologically active lipid oleamide.

Authors:  D L Boger; J E Patterson; X Guan; B F Cravatt; R A Lerner; N B Gilula
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

4.  Structural requirements for 5-HT2A and 5-HT1A serotonin receptor potentiation by the biologically active lipid oleamide.

Authors:  D L Boger; J E Patterson; Q Jin
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-14       Impact factor: 11.205

5.  Protective effect of the natural product, chaetoglobosin K, on lindane- and dieldrin-induced changes in astroglia: identification of activated signaling pathways.

Authors:  Tatyana S Sidorova; Diane F Matesic
Journal:  Pharm Res       Date:  2008-06       Impact factor: 4.200

Review 6.  Cell culture assays for chemicals with tumor-promoting or tumor-inhibiting activity based on the modulation of intercellular communication.

Authors:  I V Budunova; G M Williams
Journal:  Cell Biol Toxicol       Date:  1994-04       Impact factor: 6.691

7.  The sleep-inducing lipid oleamide deconvolutes gap junction communication and calcium wave transmission in glial cells.

Authors:  X Guan; B F Cravatt; G R Ehring; J E Hall; D L Boger; R A Lerner; N B Gilula
Journal:  J Cell Biol       Date:  1997-12-29       Impact factor: 10.539

  7 in total

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