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Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals
BACKGROUND: CD14, a receptor for lipopolysaccharides (LPS), is found in both a membrane-bound form (mCD14) and a soluble form (sCD14). It is suggested that sCD14 is mainly released from blood monocytes by serine protease-mediated shedding. Because α(1)-antitrypsin (AAT), an inhibitor of serine prote...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386460/ https://www.ncbi.nlm.nih.gov/pubmed/18426570 http://dx.doi.org/10.1186/1465-9921-9-34 |
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author | Sandström, Caroline S Novoradovskaya, Natalia Cilio, Corrado M Piitulainen, Eeva Sveger, Tomas Janciauskiene, Sabina |
author_facet | Sandström, Caroline S Novoradovskaya, Natalia Cilio, Corrado M Piitulainen, Eeva Sveger, Tomas Janciauskiene, Sabina |
author_sort | Sandström, Caroline S |
collection | PubMed |
description | BACKGROUND: CD14, a receptor for lipopolysaccharides (LPS), is found in both a membrane-bound form (mCD14) and a soluble form (sCD14). It is suggested that sCD14 is mainly released from blood monocytes by serine protease-mediated shedding. Because α(1)-antitrypsin (AAT), an inhibitor of serine proteases, has been shown to regulate CD14 expression in human monocytes in vitro, we sought to investigate plasma levels of sCD14 and monocyte expression of mCD14 in subjects at age 30 years with normal MM and deficient PiZZ and PiSZ genotypes of AAT. METHODS: Plasma levels of AAT and sCD14 were measured in 75 PiZZ and 34 PiSZ individuals with normal lung function identified from the Swedish neonatal AAT deficiency screening, and in 95 age matched PiMM controls. The mCD14 expression in monocytes from 9 PiZZ, 6 PiSZ and 11 PiMM subjects was analysed by FACS and Quantitative Real Time Reverse Transcription PCA. RESULTS: As expected, plasma AAT concentrations were PiMM>PiSZ>PiZZ (p < 0.001). Plasma sCD14 levels were higher in PiZZ than in PiMM subjects (p < 0.01). The expression level of mCD14 was higher (1.89-fold) in monocytes isolated from PiZZ subjects compared to PiMM controls (p = 0.00189). CONCLUSION: This study is the first to show higher levels of plasma sCD14 and monocyte mCD14 expression in young, clinically healthy PiZZ AAT subjects. |
format | Text |
id | pubmed-2386460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23864602008-05-16 Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals Sandström, Caroline S Novoradovskaya, Natalia Cilio, Corrado M Piitulainen, Eeva Sveger, Tomas Janciauskiene, Sabina Respir Res Research BACKGROUND: CD14, a receptor for lipopolysaccharides (LPS), is found in both a membrane-bound form (mCD14) and a soluble form (sCD14). It is suggested that sCD14 is mainly released from blood monocytes by serine protease-mediated shedding. Because α(1)-antitrypsin (AAT), an inhibitor of serine proteases, has been shown to regulate CD14 expression in human monocytes in vitro, we sought to investigate plasma levels of sCD14 and monocyte expression of mCD14 in subjects at age 30 years with normal MM and deficient PiZZ and PiSZ genotypes of AAT. METHODS: Plasma levels of AAT and sCD14 were measured in 75 PiZZ and 34 PiSZ individuals with normal lung function identified from the Swedish neonatal AAT deficiency screening, and in 95 age matched PiMM controls. The mCD14 expression in monocytes from 9 PiZZ, 6 PiSZ and 11 PiMM subjects was analysed by FACS and Quantitative Real Time Reverse Transcription PCA. RESULTS: As expected, plasma AAT concentrations were PiMM>PiSZ>PiZZ (p < 0.001). Plasma sCD14 levels were higher in PiZZ than in PiMM subjects (p < 0.01). The expression level of mCD14 was higher (1.89-fold) in monocytes isolated from PiZZ subjects compared to PiMM controls (p = 0.00189). CONCLUSION: This study is the first to show higher levels of plasma sCD14 and monocyte mCD14 expression in young, clinically healthy PiZZ AAT subjects. BioMed Central 2008 2008-04-21 /pmc/articles/PMC2386460/ /pubmed/18426570 http://dx.doi.org/10.1186/1465-9921-9-34 Text en Copyright © 2008 Sandström 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 Sandström, Caroline S Novoradovskaya, Natalia Cilio, Corrado M Piitulainen, Eeva Sveger, Tomas Janciauskiene, Sabina Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals |
title | Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals |
title_full | Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals |
title_fullStr | Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals |
title_full_unstemmed | Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals |
title_short | Endotoxin receptor CD14 in PiZ α-1-antitrypsin deficiency individuals |
title_sort | endotoxin receptor cd14 in piz α-1-antitrypsin deficiency individuals |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386460/ https://www.ncbi.nlm.nih.gov/pubmed/18426570 http://dx.doi.org/10.1186/1465-9921-9-34 |
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