Inflammatory capacity of exosomes released in the early stages of acute pancreatitis predicts the severity of the disease
Autor: | Robin Rivera, Daniel Closa, Aina Areny-Balagueró, Karina Cárdenas-Jaén, Rosa María Martin Mateos, Isabel Pascual-Moreno, Guillermo García-Rayado, Meritxell Gironella, Enrique de-Madaria, Montserrat Carrascal, Joaquín Abián |
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Přispěvatelé: | Instituto de Salud Carlos III, Asociación Española de Gastroenterología, European Commission |
Rok vydání: | 2022 |
Předmět: |
Adult
Male Proteomics Inflammation Systemic inflammation Exosomes S100A9 Pathology and Forensic Medicine S100A8 medicine Humans Pancreas Aged Aged 80 and over business.industry Middle Aged medicine.disease Microvesicles Acute pancreatitis Pancreatitis Acute Disease Immunology Disease Progression Female Tumor necrosis factor alpha medicine.symptom business Signal Transduction |
Zdroj: | Digital.CSIC. Repositorio Institucional del CSIC instname |
ISSN: | 1096-9896 0022-3417 |
Popis: | As acute pancreatitis progresses to the severe form, a life-threatening systemic inflammation is triggered. Although the mechanisms involved in this process are not yet well understood, it has been proposed that circulating exosomes may be involved in the progression of inflammation from the pancreas to distant organs. Here, the inflammatory capacity and protein profile of plasma exosomes obtained during the first 24 h of hospitalization of patients diagnosed with acute pancreatitis were characterized and compared with the final severity of the disease. We found that the final severity of the disease strongly correlates with the inflammatory capacity of exosomes in the early stages of acute pancreatitis. Exosomes isolated from patients with mild pancreatitis had no effect on macrophages, while exosomes isolated from patients with severe pancreatitis triggered NFκB activation, TNFα and IL1β expression, and free radical generation. To delve deeper into the mechanism involved, we performed a proteomic analysis of the different exosomes that allowed us to identify different groups of proteins whose concentration was also correlated with the clinical classification of pancreatitis. In particular, an increase in the amount of S100A8 and S100A9 carried by exosomes of severe pancreatitis suggests that the mechanism of action of exosomes is mediated by the effect of these proteins on NADPH oxidase. This enzyme is activated by S100A8/S100A9, thus generating free radicals and promoting an inflammatory response. Along these lines, we observed that inhibition of this enzyme abolished all the pro-inflammatory effects of exosomes from severe pancreatitis. All this suggests that the systemic effects, and therefore the final severity of acute pancreatitis, are determined by the content of circulating exosomes generated in the early hours of the process. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland. This work was supported by the projects PI16/00060 from Instituto de Salud Carlos III, 2019AEP057 CVSCI, and a grant ‘Gonzalo Miño’ from the Asociación Española de Gastroenterología. The Biologial and Environmental Proteomics group is a member of Proteored-PRB3 and is supported by Grant PT17/0019/0008 of the PE I+D+I 2013–2016, funded by ISCIII and FEDER. |
Databáze: | OpenAIRE |
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