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Oxidative stress and mitochondrial dysfunction in Kindler syndrome

BACKGROUND: Kindler Syndrome (KS) is an autosomal recessive skin disorder characterized by skin blistering, photosensitivity, premature aging, and propensity to skin cancer. In spite of the knowledge underlying cause of this disease involving mutations of FERMT1 (fermitin family member 1), and effor...

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Autores principales: Zapatero-Solana, Elisabeth, García-Giménez, Jose Luis, Guerrero-Aspizua, Sara, García, Marta, Toll, Agustí, Baselga, Eulalia, Durán-Moreno, Maria, Markovic, Jelena, García-Verdugo, Jose Manuel, Conti, Claudio J, Has, Cristina, Larcher, Fernando, Pallardó, Federico V, Del Rio, Marcela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302591/
https://www.ncbi.nlm.nih.gov/pubmed/25528446
http://dx.doi.org/10.1186/s13023-014-0211-8
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author Zapatero-Solana, Elisabeth
García-Giménez, Jose Luis
Guerrero-Aspizua, Sara
García, Marta
Toll, Agustí
Baselga, Eulalia
Durán-Moreno, Maria
Markovic, Jelena
García-Verdugo, Jose Manuel
Conti, Claudio J
Has, Cristina
Larcher, Fernando
Pallardó, Federico V
Del Rio, Marcela
author_facet Zapatero-Solana, Elisabeth
García-Giménez, Jose Luis
Guerrero-Aspizua, Sara
García, Marta
Toll, Agustí
Baselga, Eulalia
Durán-Moreno, Maria
Markovic, Jelena
García-Verdugo, Jose Manuel
Conti, Claudio J
Has, Cristina
Larcher, Fernando
Pallardó, Federico V
Del Rio, Marcela
author_sort Zapatero-Solana, Elisabeth
collection PubMed
description BACKGROUND: Kindler Syndrome (KS) is an autosomal recessive skin disorder characterized by skin blistering, photosensitivity, premature aging, and propensity to skin cancer. In spite of the knowledge underlying cause of this disease involving mutations of FERMT1 (fermitin family member 1), and efforts to characterize genotype-phenotype correlations, the clinical variability of this genodermatosis is still poorly understood. In addition, several pathognomonic features of KS, not related to skin fragility such as aging, inflammation and cancer predisposition have been strongly associated with oxidative stress. Alterations of the cellular redox status have not been previously studied in KS. Here we explored the role of oxidative stress in the pathogenesis of this rare cutaneous disease. METHODS: Patient-derived keratinocytes and their respective controls were cultured and classified according to their different mutations by PCR and western blot, the oxidative stress biomarkers were analyzed by spectrophotometry and qPCR and additionally redox biosensors experiments were also performed. The mitochondrial structure and functionality were analyzed by confocal microscopy and electron microscopy. RESULTS: Patient-derived keratinocytes showed altered levels of several oxidative stress biomarkers including MDA (malondialdehyde), GSSG/GSH ratio (oxidized and reduced glutathione) and GCL (gamma-glutamyl cysteine ligase) subunits. Electron microscopy analysis of both, KS skin biopsies and keratinocytes showed marked morphological mitochondrial abnormalities. Consistently, confocal microscopy studies of mitochondrial fluorescent probes confirmed the mitochondrial derangement. Imbalance of oxidative stress biomarkers together with abnormalities in the mitochondrial network and function are consistent with a pro-oxidant state. CONCLUSIONS: This is the first study to describe mitochondrial dysfunction and oxidative stress involvement in KS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13023-014-0211-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-43025912015-01-23 Oxidative stress and mitochondrial dysfunction in Kindler syndrome Zapatero-Solana, Elisabeth García-Giménez, Jose Luis Guerrero-Aspizua, Sara García, Marta Toll, Agustí Baselga, Eulalia Durán-Moreno, Maria Markovic, Jelena García-Verdugo, Jose Manuel Conti, Claudio J Has, Cristina Larcher, Fernando Pallardó, Federico V Del Rio, Marcela Orphanet J Rare Dis Research BACKGROUND: Kindler Syndrome (KS) is an autosomal recessive skin disorder characterized by skin blistering, photosensitivity, premature aging, and propensity to skin cancer. In spite of the knowledge underlying cause of this disease involving mutations of FERMT1 (fermitin family member 1), and efforts to characterize genotype-phenotype correlations, the clinical variability of this genodermatosis is still poorly understood. In addition, several pathognomonic features of KS, not related to skin fragility such as aging, inflammation and cancer predisposition have been strongly associated with oxidative stress. Alterations of the cellular redox status have not been previously studied in KS. Here we explored the role of oxidative stress in the pathogenesis of this rare cutaneous disease. METHODS: Patient-derived keratinocytes and their respective controls were cultured and classified according to their different mutations by PCR and western blot, the oxidative stress biomarkers were analyzed by spectrophotometry and qPCR and additionally redox biosensors experiments were also performed. The mitochondrial structure and functionality were analyzed by confocal microscopy and electron microscopy. RESULTS: Patient-derived keratinocytes showed altered levels of several oxidative stress biomarkers including MDA (malondialdehyde), GSSG/GSH ratio (oxidized and reduced glutathione) and GCL (gamma-glutamyl cysteine ligase) subunits. Electron microscopy analysis of both, KS skin biopsies and keratinocytes showed marked morphological mitochondrial abnormalities. Consistently, confocal microscopy studies of mitochondrial fluorescent probes confirmed the mitochondrial derangement. Imbalance of oxidative stress biomarkers together with abnormalities in the mitochondrial network and function are consistent with a pro-oxidant state. CONCLUSIONS: This is the first study to describe mitochondrial dysfunction and oxidative stress involvement in KS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13023-014-0211-8) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-21 /pmc/articles/PMC4302591/ /pubmed/25528446 http://dx.doi.org/10.1186/s13023-014-0211-8 Text en © Zapatero-Solana et al.; licensee BioMed Central. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zapatero-Solana, Elisabeth
García-Giménez, Jose Luis
Guerrero-Aspizua, Sara
García, Marta
Toll, Agustí
Baselga, Eulalia
Durán-Moreno, Maria
Markovic, Jelena
García-Verdugo, Jose Manuel
Conti, Claudio J
Has, Cristina
Larcher, Fernando
Pallardó, Federico V
Del Rio, Marcela
Oxidative stress and mitochondrial dysfunction in Kindler syndrome
title Oxidative stress and mitochondrial dysfunction in Kindler syndrome
title_full Oxidative stress and mitochondrial dysfunction in Kindler syndrome
title_fullStr Oxidative stress and mitochondrial dysfunction in Kindler syndrome
title_full_unstemmed Oxidative stress and mitochondrial dysfunction in Kindler syndrome
title_short Oxidative stress and mitochondrial dysfunction in Kindler syndrome
title_sort oxidative stress and mitochondrial dysfunction in kindler syndrome
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4302591/
https://www.ncbi.nlm.nih.gov/pubmed/25528446
http://dx.doi.org/10.1186/s13023-014-0211-8
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