Source:http://linkedlifedata.com/resource/pubmed/id/15273240
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2004-12-13
|
pubmed:abstractText |
Freshly isolated rat type II pneumocytes, when grown on permeable tissue culture-treated polycarbonate filters, form confluent alveolar epithelial cell monolayers (RAECM). Cells in RAECM undergo transdifferentiation, exhibiting over time morphological and phenotypic characteristics of type I pneumocytes in vivo. We recently reported that transforming growth factor-beta(1) (TGF-beta(1)) decreases overall monolayer resistance (R(te)) and stimulates short-circuit current in a dose-dependent manner. In this study, we investigated the effects of TGF-beta(1) (50 pM) or 10% newborn bovine serum (NBS) on modulation of paracellular passive ion conductance and its contribution to total passive ion conductance across RAECM. On days 5-7 in culture, tight-junctional resistance (R(tj), kOmegacm(2)) of RAECM, cultured in minimally defined serum-free medium (MDSF) with or without TGF-beta(1) or NBS, was estimated from the relationship between observed transmonolayer voltage and resistance after addition of gramicidin D to apical potassium isethionate Ringer solution under open-circuit conditions. NaCl Ringer solution bathed the basolateral side throughout the experimental period. Results showed that transmonolayer conductance (1/R(te)) and tight-junctional conductance (1/R(tj)) are 0.59 and 0.14 mS/cm(2) for control monolayers in MDSF, 1.59 and 0.38 mS/cm(2) for monolayers exposed to TGF-beta(1), and 0.38 and 0.18 mS/cm(2) for monolayers grown in the presence of NBS. The contributions to total transepithelial ion conductance by the paracellular pathway are estimated to be 23, 23, and 47% for control, TGF-beta(1)-exposed, and newborn bovine serum (NBS)-treated RAECM, respectively.
|
pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/HL 38578,
http://linkedlifedata.com/resource/pubmed/grant/HL 38621,
http://linkedlifedata.com/resource/pubmed/grant/HL 38658,
http://linkedlifedata.com/resource/pubmed/grant/HL 62569,
http://linkedlifedata.com/resource/pubmed/grant/HL 64365,
http://linkedlifedata.com/resource/pubmed/grant/HL 72231
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
8750-7587
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
98
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
138-43
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:15273240-Animals,
pubmed-meshheading:15273240-Cell Membrane,
pubmed-meshheading:15273240-Cell Membrane Permeability,
pubmed-meshheading:15273240-Cells, Cultured,
pubmed-meshheading:15273240-Computer Simulation,
pubmed-meshheading:15273240-Electric Conductivity,
pubmed-meshheading:15273240-Epithelial Cells,
pubmed-meshheading:15273240-Membrane Potentials,
pubmed-meshheading:15273240-Models, Biological,
pubmed-meshheading:15273240-Pulmonary Alveoli,
pubmed-meshheading:15273240-Rats,
pubmed-meshheading:15273240-Rats, Sprague-Dawley,
pubmed-meshheading:15273240-Respiratory Mucosa,
pubmed-meshheading:15273240-Sodium
|
pubmed:year |
2005
|
pubmed:articleTitle |
Estimation of paracellular conductance of primary rat alveolar epithelial cell monolayers.
|
pubmed:affiliation |
Dept. of Medicine, University of Southern California, Keck School of Medicine, Rm. HMR-914, 2011 Zonal Avenue, Los Angeles, CA 90033, USA. kjkim@usc.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|