4.7 Article

Inflammatory capacity of exosomes released in the early stages of acute pancreatitis predicts the severity of the disease

期刊

JOURNAL OF PATHOLOGY
卷 256, 期 1, 页码 83-92

出版社

WILEY
DOI: 10.1002/path.5811

关键词

acute pancreatitis; inflammation; exosomes

资金

  1. Instituto de Salud Carlos III [PI16/00060]
  2. Asociacion Espanola de Gastroenterologia
  3. PE I+D+I 2013-2016 - ISCIII [PT17/0019/0008]
  4. FEDER
  5. CVSCI [2019AEP057]

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This study found that the inflammatory capacity of exosomes in the early stages of acute pancreatitis strongly correlates with the final severity of the disease. The concentration of different proteins in exosomes also correlates with the clinical classification of pancreatitis. An increase in S100A8 and S100A9 in exosomes of severe pancreatitis suggests that their action is mediated by these proteins on NADPH oxidase, leading to free radical generation and inflammatory responses.
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 NF kappa B activation, TNF alpha and IL1 beta 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. (c) 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.

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