Role of Neurotransmitter and Neuromodulators in Viral Infections

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cell Microenvironment".

Deadline for manuscript submissions: closed (20 April 2023) | Viewed by 6345

Special Issue Editors


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Guest Editor
Department of Biomedical and Clinical Sciences-L. Sacco, University of Milan, 20157 Milan, Italy
Interests: viral infections; immunology; antiviral factors; genetic correlates of protection; antigen presentation
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E-Mail Website
Guest Editor
Department of Biomedical and Clinical Sciences-L. Sacco, University of Milan, 20157 Milan, Italy
Interests: viral infections; immunology; antiviral factors; genetic correlates of protection; antigen presentation

Special Issue Information

Dear Colleagues,

In light of bidirectional communication between the nervous and immune systems, neuromodulators exert potent control over innate and adaptive immune pathways and vice versa. Indeed, different neurotransmitters and neuromodulators such as norepinephrine, dopamine, acetylcholine, glutamate, vasoactive intestinal peptide, and substance P, as well as aggregation-prone proteins such as alpha-synuclein and tau, do interact with the immune system, leading to either pro- or anti-inflammatory effects, which may affect the outcome of a variety of inflammatory diseases. In turn, local or systemic inflammation affects CNS integrity, thus altering the production and subsequent release of neurotransmitters and neuromodulators in the periphery.  These effects have strong implications for immunity, and most critically in the control of infections at barrier sites, including the lung and gut mucosal epithelium, among others.

While neurotransmitters and neuromodulators are generally nerve-derived, recent studies have also demonstrated their production and relevance in peripheral sites and immune cells. In line with this, either beneficial or detrimental effects of neurotransmitters and neuromodulators have been reported in the context of viral infections. A role of neurotransmitters and CNS mediators has recently emerged in the context of SARS-CoV-2 infection, which, beyond mere neurological manifestations associated with COVID-19, may be related to systemic effects involving a plethora of diseased organs and immune cell subpopulations.

This Special Issue welcomes original studies or review articles focused on how viral infections, including that produced by SARS-CoV-2, are influenced by neurotransmitters/neuromodulators and vice versa. The aim of this Special Issue is to shed some light onto how neuromodulators, neurotransmitters, related receptors, and intracellular pathways mediate the signaling crosstalk between immune cells and diseased cells/organs in the context of viral infections.

Dr. Mara Biasin
Dr. Fiona Limanaqi
Guest Editors

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Keywords

  • neurotransmitters
  • viral infection
  • sArS-cov-2
  • innate immunity
  • adaptive immunity

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Published Papers (2 papers)

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Research

35 pages, 10196 KiB  
Article
Significance of Catecholamine Biosynthetic/Metabolic Pathway in SARS-CoV-2 Infection and COVID-19 Severity
by George Mpekoulis, Katerina I. Kalliampakou, Raphaela S. Milona, Despoina Lagou, Anastasios Ioannidis, Edison Jahaj, Christos T. Chasapis, Dionysis Kefallinos, Ioannis Karakasiliotis, Anastasia Kotanidou, Stylianos Chatzipanagiotou, Dido Vassilacopoulou, Alice G. Vassiliou, Emmanouil Angelakis and Niki Vassilaki
Cells 2023, 12(1), 12; https://doi.org/10.3390/cells12010012 - 20 Dec 2022
Cited by 7 | Viewed by 2604
Abstract
The SARS-CoV-2 infection was previously associated with the expression of the dopamine biosynthetic enzyme L-Dopa decarboxylase (DDC). Specifically, a negative correlation was detected between DDC mRNA and SARS-CoV-2 RNA levels in in vitro infected epithelial cells and the nasopharyngeal tissue of COVID-19 patients [...] Read more.
The SARS-CoV-2 infection was previously associated with the expression of the dopamine biosynthetic enzyme L-Dopa decarboxylase (DDC). Specifically, a negative correlation was detected between DDC mRNA and SARS-CoV-2 RNA levels in in vitro infected epithelial cells and the nasopharyngeal tissue of COVID-19 patients with mild/no symptoms. However, DDC, among other genes related to both DDC expression and SARS-CoV-2-infection (ACE2, dACE2, EPO), was upregulated in these patients, possibly attributed to an orchestrated host antiviral response. Herein, by comparing DDC expression in the nasopharyngeal swab samples of severe/critical to mild COVID-19 cases, we showed a 20 mean-fold reduction, highlighting the importance of the expression of this gene as a potential marker of COVID-19 severity. Moreover, we identified an association of SARS-CoV-2 infection with the expression of key catecholamine biosynthesis/metabolism-related genes, in whole blood samples from hospitalized patients and in cultured cells. Specifically, viral infection downregulated the biosynthetic part of the dopamine pathway (reduction in DDC expression up to 7.5 mean-fold), while enhanced the catabolizing part (increase in monoamine oxidases A and B expression up to 15 and 10 mean-fold, respectively) in vivo, irrespectively of the presence of comorbidities. In accordance, dopamine levels in the sera of severe cases were reduced (up to 3.8 mean-fold). Additionally, a moderate positive correlation between DDC and MAOA mRNA levels (r = 0.527, p < 00001) in the blood was identified upon SARS-CoV-2-infection. These observations were consistent to the gene expression data from SARS-CoV-2-infected Vero E6 and A549 epithelial cells. Furthermore, L-Dopa or dopamine treatment of infected cells attenuated the virus-derived cytopathic effect by 55% and 59%, respectively. The SARS-CoV-2 mediated suppression of dopamine biosynthesis in cell culture was, at least in part, attributed to hypoxia-like conditions triggered by viral infection. These findings suggest that L-Dopa/dopamine intake may have a preventive or therapeutic value for COVID-19 patients. Full article
(This article belongs to the Special Issue Role of Neurotransmitter and Neuromodulators in Viral Infections)
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23 pages, 4390 KiB  
Article
Dopamine Reduces SARS-CoV-2 Replication In Vitro through Downregulation of D2 Receptors and Upregulation of Type-I Interferons
by Fiona Limanaqi, Silvia Zecchini, Borana Dino, Sergio Strizzi, Gioia Cappelletti, Olga Utyro, Claudia Vanetti, Micaela Garziano, Irma Saulle, Mario Clerici and Mara Biasin
Cells 2022, 11(10), 1691; https://doi.org/10.3390/cells11101691 - 19 May 2022
Cited by 13 | Viewed by 2978
Abstract
Recent evidence suggests that SARS-CoV-2 hinders immune responses via dopamine (DA)-related mechanisms. Nonetheless, studies addressing the specific role of DA in the frame of SARS-CoV-2 infection are still missing. In the present study, we investigate the role of DA in SARS-CoV-2 replication along [...] Read more.
Recent evidence suggests that SARS-CoV-2 hinders immune responses via dopamine (DA)-related mechanisms. Nonetheless, studies addressing the specific role of DA in the frame of SARS-CoV-2 infection are still missing. In the present study, we investigate the role of DA in SARS-CoV-2 replication along with potential links with innate immune pathways in CaLu-3 human epithelial lung cells. We document here for the first time that, besides DA synthetic pathways, SARS-CoV-2 alters the expression of D1 and D2 DA receptors (D1DR, D2DR), while DA administration reduces viral replication. Such an effect occurs at non-toxic, micromolar-range DA doses, which are known to induce receptor desensitization and downregulation. Indeed, the antiviral effects of DA were associated with a robust downregulation of D2DRs both at mRNA and protein levels, while the amount of D1DRs was not significantly affected. While halting SARS-CoV-2 replication, DA, similar to the D2DR agonist quinpirole, upregulates the expression of ISGs and Type-I IFNs, which goes along with the downregulation of various pro-inflammatory mediators. In turn, administration of Type-I IFNs, while dramatically reducing SARS-CoV-2 replication, converges in downregulating D2DRs expression. Besides configuring the CaLu-3 cell line as a suitable model to study SARS-CoV-2-induced alterations at the level of the DA system in the periphery, our findings disclose a previously unappreciated correlation between DA pathways and Type-I IFN response, which may be disrupted by SARS-CoV-2 for host cell invasion and replication. Full article
(This article belongs to the Special Issue Role of Neurotransmitter and Neuromodulators in Viral Infections)
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