Literature DB >> 2592412

Junctional communication is induced in migrating capillary endothelial cells.

M S Pepper1, D C Spray, M Chanson, R Montesano, L Orci, P Meda.   

Abstract

Using an in vitro model in which a confluent monolayer of capillary endothelial cells is mechanically wounded, gap junction-mediated intercellular communication has been studied by loading the cells with the fluorescent dye, Lucifer Yellow. Approximately 40-50% of the cells in a nonwounded confluent monolayer were coupled in groups of four to five cells (basal level). Basal levels of communication were also observed in sparse and preconfluent cultures, but were reduced in postconfluent monolayers. 30 min after wounding, coupling was markedly reduced between cells lining the wound. Communication at the wound was partially reestablished by 2 h, exceeded basal levels after 6 h and reached a maximum after 24 h, at which stage approximately 90% of the cells were coupled in groups of six to seven cells. When the wound had closed (after 8 d), the increase in communication was no longer observed. Induction of wound-associated communication was unaffected by exposure of the cells to the DNA synthesis inhibitor mitomycin C, but was prevented by the protein synthesis inhibitor, cycloheximide. The induction of wound-associated communication was also inhibited when migration was prevented by placing the cells immediately after wounding at 22 degrees C or after exposure to cytochalasin D, suggesting that the increase in communication is dependent on cells migrating into the wound area. In contrast, migration was not prevented when coupling was blocked by exposure of the cells to retinoic acid, although this agent did disrupt the characteristic sheet-like pattern of migration typically seen during endothelial repair. These results suggest that junctional communication may play an important role in wound repair, possibly by coordinating capillary endothelial cell migration.

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Year:  1989        PMID: 2592412      PMCID: PMC2115911          DOI: 10.1083/jcb.109.6.3027

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


  34 in total

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4.  A factor from a transformed cell line that affects cell migration.

Authors:  R R Bürk
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5.  The locomotion of fibroblasts in culture. I. Movements of the leading edge.

Authors:  M Abercrombie; J E Heaysman; S M Pegrum
Journal:  Exp Cell Res       Date:  1970-03       Impact factor: 3.905

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Authors:  I Simpson; B Rose; W R Loewenstein
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7.  Cellular migration and replication in endothelial regeneration: a study using irradiated endothelial cultures.

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8.  Functional connections between cells as revealed by dye-coupling with a highly fluorescent naphthalimide tracer.

Authors:  W W Stewart
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9.  Regeneration of endothelium in rat aorta after local freezing. A scanning electron microscopic study.

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Journal:  Am J Pathol       Date:  1977-01       Impact factor: 4.307

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Authors:  S M Schwartz; C C Haudenschild; E M Eddy
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  19 in total

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Review 2.  Regulation of cellular communication by signaling microdomains in the blood vessel wall.

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

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Review 5.  Adhesion molecules and their role in cancer metastasis.

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Journal:  Cell Biophys       Date:  1993 Aug-Dec

6.  Autocrine angiotensin system regulation of bovine aortic endothelial cell migration and plasminogen activator involves modulation of proto-oncogene pp60c-src expression.

Authors:  L Bell; D J Luthringer; J A Madri; S L Warren
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7.  Role of plasminogen activator inhibitor in the reciprocal regulation of bovine aortic endothelial and smooth muscle cell migration by TGF-beta 1.

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8.  An intercellular regenerative calcium wave in porcine coronary artery endothelial cells in primary culture.

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9.  Phospholipase C-delta extends intercellular signalling range and responses to injury-released growth factors in non-excitable cells.

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10.  Effect of tumor promoting stimuli on gap junction permeability and connexin43 expression in ARL18 rat liver cell line.

Authors:  I V Budunova; G M Williams; D C Spray
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