» Articles » PMID: 36189295

Tissue-specific Pathway Activities: A Retrospective Analysis in COVID-19 Patients

Overview
Journal Front Immunol
Date 2022 Oct 3
PMID 36189295
Authors
Affiliations
Soon will be listed here.
Abstract

The ACE2 receptors essential for SARS-CoV-2 infections are expressed not only in the lung but also in many other tissues in the human body. To better understand the disease mechanisms and progression, it is essential to understand how the virus affects and alters molecular pathways in the different affected tissues. In this study, we mapped the proteomics data obtained from Nie X. (2021) to the pathway models of the COVID-19 Disease Map project and WikiPathways. The differences in pathway activities between COVID-19 and non-COVID-19 patients were calculated using the Wilcoxon test. As a result, 46% (5,235) of the detected proteins were found to be present in at least one pathway. Only a few pathways were altered in multiple tissues. As an example, the Kinin-Kallikrein pathway, an important inflammation regulatory pathway, was found to be less active in the lung, spleen, testis, and thyroid. We can confirm previously reported changes in COVID-19 patients such as the change in cholesterol, linolenic acid, and arachidonic acid metabolism, complement, and coagulation pathways in most tissues. Of all the tissues, we found the thyroid to be the organ with the most changed pathways. In this tissue, lipid pathways, energy pathways, and many COVID-19 specific pathways such as RAS and bradykinin pathways, thrombosis, and anticoagulation have altered activities in COVID-19 patients. Concluding, our results highlight the systemic nature of COVID-19 and the effect on other tissues besides the lung.

Citing Articles

WikiPathways 2024: next generation pathway database.

Agrawal A, Balci H, Hanspers K, Coort S, Martens M, Slenter D Nucleic Acids Res. 2023; 52(D1):D679-D689.

PMID: 37941138 PMC: 10767877. DOI: 10.1093/nar/gkad960.

References
1.
Coutinho M, Lacerda L, Alves S . Glycosaminoglycan storage disorders: a review. Biochem Res Int. 2011; 2012:471325. PMC: 3195295. DOI: 10.1155/2012/471325. View

2.
Brunzell J, MILLER N, Alaupovic P, St Hilaire R, Wang C, Sarson D . Familial chylomicronemia due to a circulating inhibitor of lipoprotein lipase activity. J Lipid Res. 1983; 24(1):12-9. View

3.
Gillespie M, Jassal B, Stephan R, Milacic M, Rothfels K, Senff-Ribeiro A . The reactome pathway knowledgebase 2022. Nucleic Acids Res. 2021; 50(D1):D687-D692. PMC: 8689983. DOI: 10.1093/nar/gkab1028. View

4.
Hamming I, Timens W, Bulthuis M, Lely A, Navis G, van Goor H . Tissue distribution of ACE2 protein, the functional receptor for SARS coronavirus. A first step in understanding SARS pathogenesis. J Pathol. 2004; 203(2):631-7. PMC: 7167720. DOI: 10.1002/path.1570. View

5.
Lopatko Fagerstrom I, Stahl A, Mossberg M, Tati R, Kristoffersson A, Kahn R . Blockade of the kallikrein-kinin system reduces endothelial complement activation in vascular inflammation. EBioMedicine. 2019; 47:319-328. PMC: 6796560. DOI: 10.1016/j.ebiom.2019.08.020. View