Cargando…
Marked stem cell factor expression in the airways of lung transplant recipients
BACKGROUND: Airways repair is critical to lung function following transplantation. We hypothesised that the stem cell factor (SCF) could play a role in this setting. METHODS: We studied 9 lung transplant recipients (LTx recipients) during their first year postgraft, and evaluated SCF mRNA expression...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513216/ https://www.ncbi.nlm.nih.gov/pubmed/16780589 http://dx.doi.org/10.1186/1465-9921-7-90 |
_version_ | 1782128459619762176 |
---|---|
author | Da Silva, Carla A Adda, Mélanie Stern, Marc de Blay, Frédéric Frossard, Nelly Israel-Biet, Dominique |
author_facet | Da Silva, Carla A Adda, Mélanie Stern, Marc de Blay, Frédéric Frossard, Nelly Israel-Biet, Dominique |
author_sort | Da Silva, Carla A |
collection | PubMed |
description | BACKGROUND: Airways repair is critical to lung function following transplantation. We hypothesised that the stem cell factor (SCF) could play a role in this setting. METHODS: We studied 9 lung transplant recipients (LTx recipients) during their first year postgraft, and evaluated SCF mRNA expression in bronchial biopsy specimens using on-line fluorescent PCR and SCF protein levels in bronchoalveolar lavage (BAL) and serum using ELISA. The expression of SCF receptor Kit was assessed using immunostaining of paraffin-embedded bronchial sections. RESULTS: SCF mRNA was highly expressed during the early postgraft period [Month (M)1-M3] (300% increase vs controls: 356 vs 1.2 pg SCF/μg GAPDH cDNA, p < 0.001) and decreased thereafter (M4-M12: 187 pg/μg), although remaining at all times 10–100 times higher than in controls. While SCF protein levels in BAL were similar in LTx recipients and in controls, the SCF serum levels were at all times higher in LTx recipients than in controls (p < 0.05), with no relationship between these levels and the acute complications of the graft. Finally, Kit was strongly expressed by the mast cells as well as by the bronchial epithelium of LTx recipients. CONCLUSION: SCF and Kit are expressed in bronchial biopsies from lung transplant recipients irrespective of the clinical status of the graft. A role for these factors in tissue repair following lung transplantation is hypothesised. |
format | Text |
id | pubmed-1513216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15132162006-07-20 Marked stem cell factor expression in the airways of lung transplant recipients Da Silva, Carla A Adda, Mélanie Stern, Marc de Blay, Frédéric Frossard, Nelly Israel-Biet, Dominique Respir Res Research BACKGROUND: Airways repair is critical to lung function following transplantation. We hypothesised that the stem cell factor (SCF) could play a role in this setting. METHODS: We studied 9 lung transplant recipients (LTx recipients) during their first year postgraft, and evaluated SCF mRNA expression in bronchial biopsy specimens using on-line fluorescent PCR and SCF protein levels in bronchoalveolar lavage (BAL) and serum using ELISA. The expression of SCF receptor Kit was assessed using immunostaining of paraffin-embedded bronchial sections. RESULTS: SCF mRNA was highly expressed during the early postgraft period [Month (M)1-M3] (300% increase vs controls: 356 vs 1.2 pg SCF/μg GAPDH cDNA, p < 0.001) and decreased thereafter (M4-M12: 187 pg/μg), although remaining at all times 10–100 times higher than in controls. While SCF protein levels in BAL were similar in LTx recipients and in controls, the SCF serum levels were at all times higher in LTx recipients than in controls (p < 0.05), with no relationship between these levels and the acute complications of the graft. Finally, Kit was strongly expressed by the mast cells as well as by the bronchial epithelium of LTx recipients. CONCLUSION: SCF and Kit are expressed in bronchial biopsies from lung transplant recipients irrespective of the clinical status of the graft. A role for these factors in tissue repair following lung transplantation is hypothesised. BioMed Central 2006 2006-06-16 /pmc/articles/PMC1513216/ /pubmed/16780589 http://dx.doi.org/10.1186/1465-9921-7-90 Text en Copyright © 2006 Da Silva et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Da Silva, Carla A Adda, Mélanie Stern, Marc de Blay, Frédéric Frossard, Nelly Israel-Biet, Dominique Marked stem cell factor expression in the airways of lung transplant recipients |
title | Marked stem cell factor expression in the airways of lung transplant recipients |
title_full | Marked stem cell factor expression in the airways of lung transplant recipients |
title_fullStr | Marked stem cell factor expression in the airways of lung transplant recipients |
title_full_unstemmed | Marked stem cell factor expression in the airways of lung transplant recipients |
title_short | Marked stem cell factor expression in the airways of lung transplant recipients |
title_sort | marked stem cell factor expression in the airways of lung transplant recipients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1513216/ https://www.ncbi.nlm.nih.gov/pubmed/16780589 http://dx.doi.org/10.1186/1465-9921-7-90 |
work_keys_str_mv | AT dasilvacarlaa markedstemcellfactorexpressionintheairwaysoflungtransplantrecipients AT addamelanie markedstemcellfactorexpressionintheairwaysoflungtransplantrecipients AT sternmarc markedstemcellfactorexpressionintheairwaysoflungtransplantrecipients AT deblayfrederic markedstemcellfactorexpressionintheairwaysoflungtransplantrecipients AT frossardnelly markedstemcellfactorexpressionintheairwaysoflungtransplantrecipients AT israelbietdominique markedstemcellfactorexpressionintheairwaysoflungtransplantrecipients |