Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1994-9-6
pubmed:abstractText
Bronchial epithelial cells provide a functional barrier to the movement of water and solutes between the luminal and interstitial compartments of the lung. Barrier integrity can be compromised by a variety of factors, including polycationic proteins released by inflammatory cells. We investigated the characteristics of epithelial barrier function and its modulation by cationic stimuli in canine bronchial epithelial (CBE) cells grown in culture. Morphologic characteristics were examined, and barrier function was assessed by measurements of transepithelial mannitol flux (flux) and electrical resistance (RT) during a stable, 3- to 14-day culture period. CBE cultures exhibited progressive mucociliary differentiation and contained nonciliated, ciliated, and neutral and acidic mucin-secretory cells. The synthetic polycation, poly-L-lysine (PLL), from 2.5 to 10 micrograms/ml, caused dose-related increases in flux and decreases in RT that were not accompanied by detectable release of lactate dehydrogenase (LDH) or changes in histochemical appearance. The effect on RT spontaneously reversed over a 15-h recovery period. The action of PLL on flux was not attenuated by treatment of the cells to stabilize cytoskeletal contractile elements but was immediately attenuated by the addition of heparin to the challenged cells. These results indicate that modulation of the barrier integrity of bronchial epithelial cells by cationic proteins, such as those released by inflammatory cells, represents a physiologic process that may be regulated by endogenous anionic factors.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1044-1549
pubmed:author
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
188-98
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:8049079-Animals, pubmed-meshheading:8049079-Biological Transport, pubmed-meshheading:8049079-Bronchi, pubmed-meshheading:8049079-Cell Differentiation, pubmed-meshheading:8049079-Cell Division, pubmed-meshheading:8049079-Cells, Cultured, pubmed-meshheading:8049079-Cytochalasin B, pubmed-meshheading:8049079-DNA, pubmed-meshheading:8049079-Dogs, pubmed-meshheading:8049079-Dose-Response Relationship, Drug, pubmed-meshheading:8049079-Electric Conductivity, pubmed-meshheading:8049079-Epithelial Cells, pubmed-meshheading:8049079-Epithelium, pubmed-meshheading:8049079-Heparin, pubmed-meshheading:8049079-Kinetics, pubmed-meshheading:8049079-L-Lactate Dehydrogenase, pubmed-meshheading:8049079-Mannitol, pubmed-meshheading:8049079-Phalloidine, pubmed-meshheading:8049079-Polylysine, pubmed-meshheading:8049079-Thymidine, pubmed-meshheading:8049079-Time Factors
pubmed:year
1994
pubmed:articleTitle
Physiologic modulation of bronchial epithelial cell barrier function by polycationic exposure.
pubmed:affiliation
Department of Environmental Health Sciences, Johns Hopkins School of Hygiene and Public Health, Baltimore, Maryland 21205.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.