Effects of Immunoglobulins G From Systemic ...
Type de document :
Article dans une revue scientifique: Article original
URL permanente :
Titre :
Effects of Immunoglobulins G From Systemic Sclerosis Patients in Normal Dermal Fibroblasts: A Multi-Omics Study
Auteur(s) :
Chepy, Aurelien [Auteur]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Service de médecine interne [Lille]
Vivier, Solange [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Bray, Fabrice [Auteur]
Miniaturisation pour la Synthèse, l'Analyse et la Protéomique (MSAP) - USR 3290
Ternynck, Camille [Auteur]
Evaluation des technologies de santé et des pratiques médicales - ULR 2694 [METRICS]
Meneboo, Jean-Pascal [Auteur]
Plateformes Lilloises en Biologie et Santé - UAR 2014 - US 41 [PLBS]
Figeac, Martin [Auteur]
Genomic @ Lille - PLBS [GO@L]
Plateformes Lilloises en Biologie et Santé - UAR 2014 - US 41 [PLBS]
Filiot, Alexandre [Auteur]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Guilbert, Lucile [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Institut d'Immunologie [CHRU Lille]
Jendoubi, Manel [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Rolando, Christian [Auteur]
Miniaturisation pour la Synthèse, l’Analyse et la Protéomique - UAR 3290 [MSAP]
Launay, David [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Dubucquoi, Sylvain [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Service de médecine interne [Lille]
Marot, Guillemette [Auteur]
METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694
MOdel for Data Analysis and Learning [MODAL]
Plateformes Lilloises en Biologie et Santé - UAR 2014 - US 41 [PLBS]
Sobanski, Vincent [Auteur]
Service de médecine interne [Lille]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Institut universitaire de France [IUF]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Service de médecine interne [Lille]
Vivier, Solange [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Bray, Fabrice [Auteur]

Miniaturisation pour la Synthèse, l'Analyse et la Protéomique (MSAP) - USR 3290
Ternynck, Camille [Auteur]

Evaluation des technologies de santé et des pratiques médicales - ULR 2694 [METRICS]
Meneboo, Jean-Pascal [Auteur]
Plateformes Lilloises en Biologie et Santé - UAR 2014 - US 41 [PLBS]
Figeac, Martin [Auteur]

Genomic @ Lille - PLBS [GO@L]
Plateformes Lilloises en Biologie et Santé - UAR 2014 - US 41 [PLBS]
Filiot, Alexandre [Auteur]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Guilbert, Lucile [Auteur]
Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Institut d'Immunologie [CHRU Lille]
Jendoubi, Manel [Auteur]

Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Rolando, Christian [Auteur]

Miniaturisation pour la Synthèse, l’Analyse et la Protéomique - UAR 3290 [MSAP]
Launay, David [Auteur]

Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Dubucquoi, Sylvain [Auteur]

Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
Service de médecine interne [Lille]
Marot, Guillemette [Auteur]

METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694
MOdel for Data Analysis and Learning [MODAL]
Plateformes Lilloises en Biologie et Santé - UAR 2014 - US 41 [PLBS]
Sobanski, Vincent [Auteur]

Service de médecine interne [Lille]
Institute for Translational Research in Inflammation - U 1286 [INFINITE]
Institut universitaire de France [IUF]
Titre de la revue :
Frontiers in Immunology
Nom court de la revue :
Front. Immunol.
Numéro :
13
Pagination :
904631
Éditeur :
Frontiers Media SA
Date de publication :
2022-06-29
ISSN :
1664-3224
Mot(s)-clé(s) en anglais :
systemic sclerosis
multi-omics analysis
autoantibodies
proteomics
transcriptomics
multi-omics analysis
autoantibodies
proteomics
transcriptomics
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Autoantibodies (Aabs) are frequent in systemic sclerosis (SSc). Although recognized as potent biomarkers, their pathogenic role is debated. This study explored the effect of purified immunoglobulin G (IgG) from SSc patients ...
Lire la suite >Autoantibodies (Aabs) are frequent in systemic sclerosis (SSc). Although recognized as potent biomarkers, their pathogenic role is debated. This study explored the effect of purified immunoglobulin G (IgG) from SSc patients on protein and mRNA expression of dermal fibroblasts (FBs) using an innovative multi-omics approach. Dermal FBs were cultured in the presence of sera or purified IgG from patients with diffuse cutaneous SSc (dcSSc), limited cutaneous SSc or healthy controls (HCs). The FB proteome and transcriptome were explored using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) and microarray assays, respectively. Proteomic analysis identified 3,310 proteins. SSc sera and purified IgG induced singular protein profile patterns. These FB proteome changes depended on the Aab serotype, with a singular effect observed with purified IgG from anti-topoisomerase-I autoantibody (ATA) positive patients compared to HC or other SSc serotypes. IgG from ATA positive SSc patients induced enrichment in proteins involved in focal adhesion, cadherin binding, cytosolic part, or lytic vacuole. Multi-omics analysis was performed in two ways: first by restricting the analysis of the transcriptomic data to differentially expressed proteins; and secondly, by performing a global statistical analysis integrating proteomics and transcriptomics. Transcriptomic analysis distinguished 764 differentially expressed genes and revealed that IgG from dcSSc can induce extracellular matrix (ECM) remodeling changes in gene expression profiles in FB. Global statistical analysis integrating proteomics and transcriptomics confirmed that IgG from SSc can induce ECM remodeling and activate FB profiles. This effect depended on the serotype of the patient, suggesting that SSc Aab might play a pathogenic role in some SSc subsets.Lire moins >
Lire la suite >Autoantibodies (Aabs) are frequent in systemic sclerosis (SSc). Although recognized as potent biomarkers, their pathogenic role is debated. This study explored the effect of purified immunoglobulin G (IgG) from SSc patients on protein and mRNA expression of dermal fibroblasts (FBs) using an innovative multi-omics approach. Dermal FBs were cultured in the presence of sera or purified IgG from patients with diffuse cutaneous SSc (dcSSc), limited cutaneous SSc or healthy controls (HCs). The FB proteome and transcriptome were explored using liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS) and microarray assays, respectively. Proteomic analysis identified 3,310 proteins. SSc sera and purified IgG induced singular protein profile patterns. These FB proteome changes depended on the Aab serotype, with a singular effect observed with purified IgG from anti-topoisomerase-I autoantibody (ATA) positive patients compared to HC or other SSc serotypes. IgG from ATA positive SSc patients induced enrichment in proteins involved in focal adhesion, cadherin binding, cytosolic part, or lytic vacuole. Multi-omics analysis was performed in two ways: first by restricting the analysis of the transcriptomic data to differentially expressed proteins; and secondly, by performing a global statistical analysis integrating proteomics and transcriptomics. Transcriptomic analysis distinguished 764 differentially expressed genes and revealed that IgG from dcSSc can induce extracellular matrix (ECM) remodeling changes in gene expression profiles in FB. Global statistical analysis integrating proteomics and transcriptomics confirmed that IgG from SSc can induce ECM remodeling and activate FB profiles. This effect depended on the serotype of the patient, suggesting that SSc Aab might play a pathogenic role in some SSc subsets.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
CHU Lille
CHU Lille
Collections :
Date de dépôt :
2022-12-06T16:05:48Z
2022-12-06T16:34:12Z
2022-12-14T13:35:02Z
2022-12-06T16:34:12Z
2022-12-14T13:35:02Z
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