Literature DB >> 3045419

Junctional transfer in wounded cultures of bovine aortic endothelial cells.

D M Larson1, C C Haudenschild.   

Abstract

Both in vivo and in vitro, endothelial cells form continuous monolayers displaying growth control by cell density as well as cell contact. Several functions of endothelium are dependent upon maintenance of an intact monolayer. When such a monolayer is injured, endothelial cells migrate out from the wound edges and proliferate to cover the area of denudation. The response of endothelium to wounding is therefore a matter of both growth control and cellular motility. Since intercellular gap junctions have been postulated to have a role in growth control, we set out to determine whether junctional communication was altered in the activated, migrating cells. We found extensive transfer of microinjected fluorescent dye molecules (Lucifer yellow CH) in cells at or near the wound edge at various times after wounding (1 minute to 48 hours). However, cells near a wound edge transferred dye at a frequency significantly diminished from that observed in undisturbed monolayers (81.1 +/- 1.5 (SE) versus 92.7 +/- 0.8% of adjacent cells received dye). There was a significant positive correlation between transfer frequency and distance from the wound (expressed as intervening cells) but not between transfer frequency and time after wounding. These results suggest that endothelial cells in a wounded monolayer retain junctional communication at a slightly but significantly reduced level and that increased motility and the wound healing response do not necessarily correlate with total loss of communication.

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Year:  1988        PMID: 3045419

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  7 in total

1.  Inhibition of endothelial wound repair by dominant negative connexin inhibitors.

Authors:  B R Kwak; M S Pepper; D B Gros; P Meda
Journal:  Mol Biol Cell       Date:  2001-04       Impact factor: 4.138

2.  Decreased blood flow rate disrupts endothelial repair in vivo.

Authors:  S Vyalov; B L Langille; A I Gotlieb
Journal:  Am J Pathol       Date:  1996-12       Impact factor: 4.307

3.  Modulation of gap junction-mediated intercellular communication in embryonic chick mesenchyme during tissue remodeling in vitro.

Authors:  S B Parker; E L Hertzberg; R Minkoff
Journal:  Cell Tissue Res       Date:  1994-02       Impact factor: 5.249

4.  Differential migration and proliferation of geometrical ensembles of cell clusters.

Authors:  Girish Kumar; Bo Chen; Carlos C Co; Chia-Chi Ho
Journal:  Exp Cell Res       Date:  2011-02-19       Impact factor: 3.905

5.  Gap junctional communication between vascular cells. Induction of connexin43 messenger RNA in macrophage foam cells of atherosclerotic lesions.

Authors:  D Polacek; R Lal; M V Volin; P F Davies
Journal:  Am J Pathol       Date:  1993-02       Impact factor: 4.307

6.  Junctional communication is induced in migrating capillary endothelial cells.

Authors:  M S Pepper; D C Spray; M Chanson; R Montesano; L Orci; P Meda
Journal:  J Cell Biol       Date:  1989-12       Impact factor: 10.539

7.  Suppressive effect of irsogladine maleate on diethylnitrosamine-initiated and phenobarbital-promoted hepatocarcinogenesis in male F344 rats.

Authors:  S Sugie; K Okamoto; F Ueda; T Watanabe; T Tanaka; H Mori
Journal:  Jpn J Cancer Res       Date:  1998-04
  7 in total

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