Your browser doesn't support javascript.
loading
Fatty Acid and Carnitine Metabolism Are Dysregulated in Systemic Sclerosis Patients.
Ottria, A; Hoekstra, A T; Zimmermann, M; van der Kroef, M; Vazirpanah, N; Cossu, M; Chouri, E; Rossato, M; Beretta, L; Tieland, R G; Wichers, C G K; Stigter, E; Gulersonmez, C; Bonte-Mineur, F; Berkers, C R; Radstake, T R D J; Marut, W.
Affiliation
  • Ottria A; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Hoekstra AT; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Zimmermann M; Biomolecular Mass Spectrometry and Proteomics, Bijvoet Center for Biomolecular Research, Utrecht University, Utrecht, Netherlands.
  • van der Kroef M; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Vazirpanah N; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Cossu M; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Chouri E; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Rossato M; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Beretta L; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Tieland RG; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Wichers CGK; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Stigter E; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Gulersonmez C; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Bonte-Mineur F; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Berkers CR; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Radstake TRDJ; Referral Center for Systemic Autoimmune Diseases, University of Milan and Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena, Milan, Italy.
  • Marut W; Center for Translational Immunology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Front Immunol ; 11: 822, 2020.
Article in En | MEDLINE | ID: mdl-32528464
ABSTRACT
Systemic sclerosis (SSc) is a rare chronic disease of unknown pathogenesis characterized by fibrosis of the skin and internal organs, vascular alteration, and dysregulation of the immune system. In order to better understand the immune system and its perturbations leading to diseases, the study of the mechanisms regulating cellular metabolism has gained a widespread interest. Here, we have assessed the metabolic status of plasma and dendritic cells (DCs) in patients with SSc. We identified a dysregulated metabolomic signature in carnitine in circulation (plasma) and intracellularly in DCs of SSc patients. In addition, we confirmed carnitine alteration in the circulation of SSc patients in three independent plasma measurements from two different cohorts and identified dysregulation of fatty acids. We hypothesized that fatty acid and carnitine alterations contribute to potentiation of inflammation in SSc. Incubation of healthy and SSc dendritic cells with etoposide, a carnitine transporter inhibitor, inhibited the production of pro-inflammatory cytokines such as IL-6 through inhibition of fatty acid oxidation. These findings shed light on the altered metabolic status of the immune system in SSc patients and opens up for potential novel avenues to reduce inflammation.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Scleroderma, Systemic / Carnitine / Fatty Acids Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2020 Document type: Article Affiliation country: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Scleroderma, Systemic / Carnitine / Fatty Acids Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2020 Document type: Article Affiliation country: Netherlands