High levels of extracellular ATP lead to different inflammatory responses in COVID-19 patients according to the severity.


Journal

Journal of molecular medicine (Berlin, Germany)
ISSN: 1432-1440
Titre abrégé: J Mol Med (Berl)
Pays: Germany
ID NLM: 9504370

Informations de publication

Date de publication:
04 2022
Historique:
received: 02 12 2021
accepted: 23 02 2022
revised: 21 02 2022
pubmed: 7 3 2022
medline: 2 4 2022
entrez: 6 3 2022
Statut: ppublish

Résumé

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has significantly impacted the world and has driven many researchers into the pathophysiology of COVID-19. In the findings, there is a close association between purinergic signaling and the immune response. Then, this study aimed to evaluate alterations in the purinergic signaling in COVID-19 patients according to range severity. We divided the COVID-19 patients into moderate and severe cases following the guideless of NIH and WHO, together with clinical characteristics. The blood samples were collected to obtain PBMCs and platelets. We analyzed the ectonucleotidase activities through ATP, ADP, AMP, Ado hydrolysis, E-NTPDase1 (CD39), and 5'-NT (CD73) expression by flow cytometry in total leukocytes. The extracellular ATP was measured by bioluminescence, and cytokines were analyzed by flow cytometry. We observed a decrease in ATP hydrolysis and increased AMP hydrolysis in PBMCs for both groups. In severe cases, ATP hydrolysis was raised for the platelets, while ADP and AMP hydrolysis have risen significantly in both groups. Additionally, there was a significant increase in ADP hydrolysis in severe cases compared to moderate cases. In addition, we observed an increase in the ADA activity in platelets of moderate patients. Moderate and severe cases showed increased expression of CD39 and CD73 in total leukocytes. To finalize the purinergic signaling, extracellular ATP was increased in both groups. Furthermore, there was an increase in IL-2, IL-6, IL-10, and IL-17 in moderate and severe groups. Thus, for the first time, our findings confirm the changes in purinergic signaling and immune response in COVID-19, in addition to making it more evident that the severity range directly impacts these changes. Therefore, the therapeutic potential of the purinergic system must be highlighted and studied as a possible target for the treatment of SARS-CoV-2 disease. KEY MESSAGES: COVID-19 patients exhibit alterations in purinergic system and immune response. High levels of extracellular ATP lead to different inflammatory responses. CD39 and CD73 expression were increased in COVID-19 patients. Cytokines IL-2, IL-6, IL-10, and IL-17 also were altered in these patients. The purinergic system may be a possibility target to SARS-CoV-2 treatments.

Identifiants

pubmed: 35249135
doi: 10.1007/s00109-022-02185-4
pii: 10.1007/s00109-022-02185-4
pmc: PMC8898096
doi:

Substances chimiques

Adenosine Triphosphate 8L70Q75FXE

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

645-663

Subventions

Organisme : CNPq
ID : 404256/2021-0

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Gilnei Bruno da Silva (GB)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Daiane Manica (D)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Alana Patrícia da Silva (AP)

Graduate Program in Science and Food Technology, Federal University of Fronteira Sul, Laranjeiras Do Sul, PR, Brazil.

Greicy Cristine Kosvoski (GC)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Marceli Hanauer (M)

Graduate Program in Nursing, Federal University of Santa Catarina, Florianópolis, SC, Brazil.

Charles Elias Assmann (CE)

Graduate Program in Biological Sciences: Toxicological Biochemistry, Department of Biochemistry and Molecular Biology, Federal University of Santa Maria, Santa Maria, RS, Brazil.

Júlia Leão Batista Simões (JLB)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Micheli Mainardi Pillat (MM)

Graduate Program in Pharmaceutical Sciences, Department of Microbiology and Parasitology, Federal University of Santa Maria, Santa Maria, RS, Brazil.

Jéssica Dotto de Lara (JD)

Graduate Program in Pharmaceutical Sciences, Department of Microbiology and Parasitology, Federal University of Santa Maria, Santa Maria, RS, Brazil.

Filomena Marafon (F)

Graduate Program in Biochemistry, Department of Biological Science, Federal University of Santa Catarina, Florianópolis, SC, Brazil.

Amanda Gollo Bertollo (AG)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Maiqueli E D Mingoti (MED)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Jullye Gavioli (J)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Gislaine Zilli Réus (GZ)

Graduate Program in Health Sciences, Department of Translational Psychiatry, University of the Extreme South of Santa Catarina, SC, Criciúma, Brazil.

Gabriela Gonçalves de Oliveira (GG)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Zuleide Maria Ignácio (ZM)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil.

Margarete Dulce Bagatini (MD)

Graduate Program in Biomedical Sciences, Federal University of Fronteira Sul, SC, Chapecó, Brazil. margaretebagatini@yahoo.com.br.

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