Tubular bridges for bronchial epithelial cell migration and communication

Background: Biological processes from embryogenesis to tumorigenesis rely on the coordinated coalescence of cells and synchronized cell-to-cell communication. Intercellular signaling enables cell masses to communicate through endocrine pathways at a distance or by direct contact over shorter dimensi...

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Bibliographic Details
Main Authors: Zani, Brett Greer (Contributor), Indolfi, Laura (Contributor), Edelman, Elazer R. (Contributor)
Other Authors: Harvard University- (Contributor)
Format: Article
Language:English
Published: Public Library of Science, 2010-05-10T16:29:17Z.
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Online Access:Get fulltext
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042 |a dc 
100 1 0 |a Zani, Brett Greer  |e author 
100 1 0 |a Harvard University-  |e contributor 
100 1 0 |a Edelman, Elazer R.  |e contributor 
100 1 0 |a Zani, Brett Greer  |e contributor 
100 1 0 |a Indolfi, Laura  |e contributor 
100 1 0 |a Edelman, Elazer R.  |e contributor 
700 1 0 |a Indolfi, Laura  |e author 
700 1 0 |a Edelman, Elazer R.  |e author 
245 0 0 |a Tubular bridges for bronchial epithelial cell migration and communication 
260 |b Public Library of Science,   |c 2010-05-10T16:29:17Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/54740 
520 |a Background: Biological processes from embryogenesis to tumorigenesis rely on the coordinated coalescence of cells and synchronized cell-to-cell communication. Intercellular signaling enables cell masses to communicate through endocrine pathways at a distance or by direct contact over shorter dimensions. Cellular bridges, the longest direct connections between cells, facilitate transfer of cellular signals and components over hundreds of microns in vitro and in vivo. Methodology/Principal Findings: Using various cellular imaging techniques on human tissue cultures, we identified two types of tubular, bronchial epithelial (EP) connections, up to a millimeter in length, designated EP bridges. Structurally distinct from other cellular connections, the first type of EP bridge may mediate transport of cellular material between cells, while the second type of EP bridge is functionally distinct from all other cellular connections by mediating migration of epithelial cells between EP masses. Morphological and biochemical interactions with other cell types differentially regulated the nuclear factor-kB and cyclooxygenase inflammatory pathways, resulting in increased levels of inflammatory molecules that impeded EP bridge formation. Pharmacologic inhibition of these inflammatory pathways caused increased morphological and mobility changes stimulating the biogenesis of EP bridges, in part through the upregulation of reactive oxygen species pathways. Conclusions/Significance: EP bridge formation appears to be a normal response of EP physiology in vitro, which is differentially inhibited by inflammatory cellular pathways depending upon the morphological and biochemical interactions between EP cells and other cell types. These tubular EP conduits may represent an ultra long-range form of direct intercellular communication and a completely new mechanism of tissue-mediated cell migration. 
520 |a United States. National Institutes of Health (R01 GM 49039) 
546 |a en_US 
655 7 |a Article 
773 |t PLoS ONE