» Articles » PMID: 35625805

Skeletal Muscle and COVID-19: The Potential Involvement of Bioactive Sphingolipids

Overview
Journal Biomedicines
Date 2022 May 28
PMID 35625805
Authors
Affiliations
Soon will be listed here.
Abstract

SARS-CoV-2 virus infection is the cause of the coronavirus disease 2019 (COVID-19), which is still spreading over the world. The manifestation of this disease can range from mild to severe and can be limited in time (weeks) or persist for months in about 30-50% of patients. COVID-19 is considered a multiple organ dysfunction syndrome and the musculoskeletal system manifestations are beginning to be considered of absolute importance in both COVID-19 patients and in patients recovering from the SARS-CoV-2 infection. Musculoskeletal manifestations of COVID-19 and other coronavirus infections include loss of muscle mass, muscle weakness, fatigue or myalgia, and muscle injury. The molecular mechanisms by which SARS-CoV-2 can cause damage to skeletal muscle (SkM) cells are not yet well understood. Sphingolipids (SLs) represent an important class of eukaryotic lipids with structural functions as well as bioactive molecules able to modulate crucial processes, including inflammation and viral infection. In the last two decades, several reports have highlighted the role of SLs in modulating SkM cell differentiation, regeneration, aging, response to insulin, and contraction. This review summarizes the consequences of SARS-CoV-2 infection on SkM and the potential involvement of SLs in the tissue responses to virus infection. In particular, we highlight the role of sphingosine 1-phosphate signaling in order to aid the prediction of novel targets for preventing and/or treating acute and long-term musculoskeletal manifestations of virus infection in COVID-19.

Citing Articles

Proteomic and metabolomic profiling of plasma uncovers immune responses in patients with Long COVID-19.

Wei Y, Gu H, Ma J, Mao X, Wang B, Wu W Front Microbiol. 2025; 15():1470193.

PMID: 39802657 PMC: 11718655. DOI: 10.3389/fmicb.2024.1470193.


The Sphingolipid-Signaling Pathway as a Modulator of Infection by SARS-CoV-2.

Fenizia S, Gaggini M, Vassalle C Curr Issues Mol Biol. 2023; 45(10):7956-7973.

PMID: 37886946 PMC: 10605018. DOI: 10.3390/cimb45100503.


Statin Use in Relation to COVID-19 and Other Respiratory Infections: Muscle and Other Considerations.

Golomb B, Han J, Langsjoen P, Dinkeloo E, Zemljic-Harpf A J Clin Med. 2023; 12(14).

PMID: 37510774 PMC: 10380486. DOI: 10.3390/jcm12144659.


Irisin Is Target of Sphingosine-1-Phosphate/Sphingosine-1-Phosphate Receptor-Mediated Signaling in Skeletal Muscle Cells.

Pierucci F, Chirco A, Meacci E Int J Mol Sci. 2023; 24(13).

PMID: 37445724 PMC: 10341824. DOI: 10.3390/ijms241310548.


Musculoskeletal involvement: COVID-19 and post COVID 19.

Evcik D Turk J Phys Med Rehabil. 2023; 69(1):1-7.

PMID: 37201006 PMC: 10186015. DOI: 10.5606/tftrd.2023.12521.


References
1.
Zimniak M, Kirschner L, Hilpert H, Geiger N, Danov O, Oberwinkler H . The serotonin reuptake inhibitor Fluoxetine inhibits SARS-CoV-2 in human lung tissue. Sci Rep. 2021; 11(1):5890. PMC: 7961020. DOI: 10.1038/s41598-021-85049-0. View

2.
Adeola O, Olugasa B, Emikpe B . Molecular detection of influenza A(H1N1)pdm09 viruses with M genes from human pandemic strains among Nigerian pigs, 2013-2015: implications and associated risk factors. Epidemiol Infect. 2017; 145(16):3345-3360. PMC: 9148760. DOI: 10.1017/S0950268817002503. View

3.
Wu Z, McGoogan J . Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention. JAMA. 2020; 323(13):1239-1242. DOI: 10.1001/jama.2020.2648. View

4.
Bezgovsek J, Gulbins E, Friedrich S, Lang K, Duhan V . Sphingolipids in early viral replication and innate immune activation. Biol Chem. 2018; 399(10):1115-1123. DOI: 10.1515/hsz-2018-0181. View

5.
DAprile C, Prioni S, Mauri L, Prinetti A, Grassi S . Lipid rafts as platforms for sphingosine 1-phosphate metabolism and signalling. Cell Signal. 2021; 80:109929. DOI: 10.1016/j.cellsig.2021.109929. View