Platelet-Derived Extracellular Vesicles as Lipid Carriers in Severe Allergic Inflammation

Author:

Couto-Rodriguez Alba1ORCID,Villaseñor Alma12ORCID,Pablo-Torres Carmela1,Obeso David12,Rey-Stolle María Fernanda2ORCID,Peinado Héctor3ORCID,Bueno José Luis4,Reaño-Martos Mar5,Iglesias Cadarso Alfredo5,Gomez-Casado Cristina1,Barbas Coral2ORCID,Barber Domingo1ORCID,Escribese María M.1ORCID,Izquierdo Elena1ORCID

Affiliation:

1. Departamento de Ciencias Médicas Básicas, Instituto de Medicina Molecular Aplicada (IMMA) Nemesio Díez, Facultad de Medicina, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain

2. Centro de Metabolómica y Bioanálisis (CEMBIO), Facultad de Farmacia, Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, 28660 Boadilla del Monte, Spain

3. Spanish National Cancer Research Center (CNIO), Molecular Oncology Programme, Microenvironment and Metastasis Laboratory, 28029 Madrid, Spain

4. Department of Hematology, Hospital Universitario Puerta de Hierro Majadahonda, 28222 Madrid, Spain

5. Department of Allergy and Immunology, Hospital Universitario Puerta de Hierro Majadahonda, 28222 Madrid, Spain

Abstract

The resolution of inflammation is a complex process that is critical for removing inflammatory cells and restoring tissue function. The dysregulation of these mechanisms leads to chronic inflammatory disorders. Platelets, essential cells for preserving homeostasis, are thought to play a role in inflammation as they are a source of immunomodulatory factors. Our aim was to identify key metabolites carried by platelet-derived extracellular vesicles (PL-EVs) in a model of allergic inflammation. PL-EVs were isolated by serial ultracentrifugation using platelet-rich plasma samples obtained from platelet apheresis from severely (n = 6) and mildly (n = 6) allergic patients and non-allergic individuals used as controls (n = 8). PL-EVs were analysed by a multiplatform approach using liquid and gas chromatography coupled to mass spectrometry (LC-MS and GC-MS, respectively). PL-EVs obtained from severely and mildly allergic patients and control individuals presented comparable particle concentrations and sizes with similar protein concentrations. Strikingly, PL-EVs differed in their lipid and metabolic content according to the severity of inflammation. L-carnitine, ceramide (Cer (d18:0/24:0)), and several triglycerides, all of which seem to be involved in apoptosis and regulatory T functions, were higher in PL-EVs from patients with mild allergic inflammation than in those with severe inflammation. In contrast, PL-EVs obtained from patients with severe allergic inflammation showed an alteration in the arachidonic acid pathway. This study demonstrates that PL-EVs carry specific lipids and metabolites according to the degree of inflammation in allergic patients and propose novel perspectives for characterising the progression of allergic inflammation.

Funder

ISCIII

FEDER “Investing in your future”

RICORS “Red de Enfermedades Inflamatorias (REI)”

Ministry of Science and Innovation in Spain

European program ERA HDHL—Nutrition & the Epigenome

Project Dietary Intervention in Food Allergy: Microbiome

Epigenetic and Metabolomic Interactions DIFAMEM

Fundación Mutua Madrileña

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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