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The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium
To test the hypothesis that mononuclear cell products could increase the expression of HLA-DR and ICAM-1 molecules in bronchial epithelial cells (BECs), subconfluent cultures of human BECs, obtained from surgically resected bronchi, were incubated with PHA-activated blood mononuclear cell conditione...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1994
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365596/ https://www.ncbi.nlm.nih.gov/pubmed/18475607 http://dx.doi.org/10.1155/S0962935194000682 |
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author | Sacco, O. Lantero, S. Scarso, L. Frangova, V. Ottolini, V. Rossi, G. A. |
author_facet | Sacco, O. Lantero, S. Scarso, L. Frangova, V. Ottolini, V. Rossi, G. A. |
author_sort | Sacco, O. |
collection | PubMed |
description | To test the hypothesis that mononuclear cell products could increase the expression of HLA-DR and ICAM-1 molecules in bronchial epithelial cells (BECs), subconfluent cultures of human BECs, obtained from surgically resected bronchi, were incubated with PHA-activated blood mononuclear cell conditioned media (BCM-CM) or recombinant IFN-γ. The presence of HLA-DR and ICAM-1 molecules on BECs was then evaluated by specific antibody staining and flow-cytometry analysis. The addition to BEC cultures of different concentrations of PHA-stimulated BMC-CM, or of IFN-γ induced a dosedependent increase of HIA-DR and ICAM-1 expression, while no effect was observed with unstimulated BMC-CM. The ability of nedocromil sodium and, as control, of dexamethasone, to prevent the upregulation of HLA-DR and ICAM-1 expression on BECs was then tested. Increasing concentrations (10(−7) to 10(−4) M) of nedocromil significandy inhibited HLA-DR and ICAM-1 expression by BECs in a dose-dependent fashion. A similarly dose-dependent inhibitory effect was also observed with dexamethasone, which, however, was less active than nedocromil on HL-ADR expression and more active on ICAM-1 expression. Finally, nedocromil and dexamethasone showed a significant synergistic effect on the expression of both cell surface molecules at the lowest concentrations tested. |
format | Text |
id | pubmed-2365596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23655962008-05-12 The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium Sacco, O. Lantero, S. Scarso, L. Frangova, V. Ottolini, V. Rossi, G. A. Mediators Inflamm Research Article To test the hypothesis that mononuclear cell products could increase the expression of HLA-DR and ICAM-1 molecules in bronchial epithelial cells (BECs), subconfluent cultures of human BECs, obtained from surgically resected bronchi, were incubated with PHA-activated blood mononuclear cell conditioned media (BCM-CM) or recombinant IFN-γ. The presence of HLA-DR and ICAM-1 molecules on BECs was then evaluated by specific antibody staining and flow-cytometry analysis. The addition to BEC cultures of different concentrations of PHA-stimulated BMC-CM, or of IFN-γ induced a dosedependent increase of HIA-DR and ICAM-1 expression, while no effect was observed with unstimulated BMC-CM. The ability of nedocromil sodium and, as control, of dexamethasone, to prevent the upregulation of HLA-DR and ICAM-1 expression on BECs was then tested. Increasing concentrations (10(−7) to 10(−4) M) of nedocromil significandy inhibited HLA-DR and ICAM-1 expression by BECs in a dose-dependent fashion. A similarly dose-dependent inhibitory effect was also observed with dexamethasone, which, however, was less active than nedocromil on HL-ADR expression and more active on ICAM-1 expression. Finally, nedocromil and dexamethasone showed a significant synergistic effect on the expression of both cell surface molecules at the lowest concentrations tested. Hindawi Publishing Corporation 1994 /pmc/articles/PMC2365596/ /pubmed/18475607 http://dx.doi.org/10.1155/S0962935194000682 Text en Copyright © 1994 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sacco, O. Lantero, S. Scarso, L. Frangova, V. Ottolini, V. Rossi, G. A. The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium |
title | The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial
Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium |
title_full | The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial
Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium |
title_fullStr | The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial
Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium |
title_full_unstemmed | The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial
Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium |
title_short | The Increased Expression of HLA-DR and ICAM-1 Molecules by Human Bronchial Epithelial
Cells, Induced by Activated Mononuclear Cells, is Downregulated by Nedocromil Sodium |
title_sort | increased expression of hla-dr and icam-1 molecules by human bronchial epithelial
cells, induced by activated mononuclear cells, is downregulated by nedocromil sodium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365596/ https://www.ncbi.nlm.nih.gov/pubmed/18475607 http://dx.doi.org/10.1155/S0962935194000682 |
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