Mechanisms of the noxious inflammatory cycle in cystic fibrosis

<p>Abstract</p> <p>Multiple evidences indicate that inflammation is an event occurring prior to infection in patients with cystic fibrosis. The self-perpetuating inflammatory cycle may play a pathogenic part in this disease. The role of the NF-κB pathway in enhanced production of i...

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Main Authors: Freyssinet Jean-Marie, Rottner Mathilde, Martínez M Carmen
Format: Article
Language:English
Published: BMC 2009-03-01
Series:Respiratory Research
Online Access:http://respiratory-research.com/content/10/1/23
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spelling doaj-03867333d21d489cb4664bd743be19bf2020-11-25T01:58:30ZengBMCRespiratory Research1465-99212009-03-011012310.1186/1465-9921-10-23Mechanisms of the noxious inflammatory cycle in cystic fibrosisFreyssinet Jean-MarieRottner MathildeMartínez M Carmen<p>Abstract</p> <p>Multiple evidences indicate that inflammation is an event occurring prior to infection in patients with cystic fibrosis. The self-perpetuating inflammatory cycle may play a pathogenic part in this disease. The role of the NF-κB pathway in enhanced production of inflammatory mediators is well documented. The pathophysiologic mechanisms through which the intrinsic inflammatory response develops remain unclear. The unfolded mutated protein cystic fibrosis transmembrane conductance regulator (CFTRΔF508), accounting for this pathology, is retained in the endoplasmic reticulum (ER), induces a stress, and modifies calcium homeostasis. Furthermore, CFTR is implicated in the transport of glutathione, the major antioxidant element in cells. CFTR mutations can alter redox homeostasis and induce an oxidative stress. The disturbance of the redox balance may evoke NF-κB activation and, in addition, promote apoptosis. In this review, we examine the hypotheses of the integrated pathogenic processes leading to the intrinsic inflammatory response in cystic fibrosis.</p> http://respiratory-research.com/content/10/1/23
collection DOAJ
language English
format Article
sources DOAJ
author Freyssinet Jean-Marie
Rottner Mathilde
Martínez M Carmen
spellingShingle Freyssinet Jean-Marie
Rottner Mathilde
Martínez M Carmen
Mechanisms of the noxious inflammatory cycle in cystic fibrosis
Respiratory Research
author_facet Freyssinet Jean-Marie
Rottner Mathilde
Martínez M Carmen
author_sort Freyssinet Jean-Marie
title Mechanisms of the noxious inflammatory cycle in cystic fibrosis
title_short Mechanisms of the noxious inflammatory cycle in cystic fibrosis
title_full Mechanisms of the noxious inflammatory cycle in cystic fibrosis
title_fullStr Mechanisms of the noxious inflammatory cycle in cystic fibrosis
title_full_unstemmed Mechanisms of the noxious inflammatory cycle in cystic fibrosis
title_sort mechanisms of the noxious inflammatory cycle in cystic fibrosis
publisher BMC
series Respiratory Research
issn 1465-9921
publishDate 2009-03-01
description <p>Abstract</p> <p>Multiple evidences indicate that inflammation is an event occurring prior to infection in patients with cystic fibrosis. The self-perpetuating inflammatory cycle may play a pathogenic part in this disease. The role of the NF-κB pathway in enhanced production of inflammatory mediators is well documented. The pathophysiologic mechanisms through which the intrinsic inflammatory response develops remain unclear. The unfolded mutated protein cystic fibrosis transmembrane conductance regulator (CFTRΔF508), accounting for this pathology, is retained in the endoplasmic reticulum (ER), induces a stress, and modifies calcium homeostasis. Furthermore, CFTR is implicated in the transport of glutathione, the major antioxidant element in cells. CFTR mutations can alter redox homeostasis and induce an oxidative stress. The disturbance of the redox balance may evoke NF-κB activation and, in addition, promote apoptosis. In this review, we examine the hypotheses of the integrated pathogenic processes leading to the intrinsic inflammatory response in cystic fibrosis.</p>
url http://respiratory-research.com/content/10/1/23
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AT rottnermathilde mechanismsofthenoxiousinflammatorycycleincysticfibrosis
AT martinezmcarmen mechanismsofthenoxiousinflammatorycycleincysticfibrosis
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