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Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?

Although SARS-CoV-2 viral attacks starts by the interaction of spike protein (S Protein) to ACE2 receptor located at the cell surface of respiratory tract and digestive system cells, different endocrine targets, endocrine organs and metabolic conditions are of fundamental relevance for understanding...

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Detalles Bibliográficos
Autores principales: Soldevila, Berta, Puig-Domingo, Manel, Marazuela, Mónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325622/
https://www.ncbi.nlm.nih.gov/pubmed/34333732
http://dx.doi.org/10.1007/s11154-021-09678-6
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author Soldevila, Berta
Puig-Domingo, Manel
Marazuela, Mónica
author_facet Soldevila, Berta
Puig-Domingo, Manel
Marazuela, Mónica
author_sort Soldevila, Berta
collection PubMed
description Although SARS-CoV-2 viral attacks starts by the interaction of spike protein (S Protein) to ACE2 receptor located at the cell surface of respiratory tract and digestive system cells, different endocrine targets, endocrine organs and metabolic conditions are of fundamental relevance for understanding disease progression and special outcomes, in particular those of fatal consequences for the patient. During pandemic, moreover, a specific phenotype of COVID-19 metabolic patient has been described, characterized by being at particular risk of worse outcomes. In the present paper we describe the mechanism of viral interaction with endocrine organs, emphasizing the specific endocrine molecules of particular relevance explaining COVID-19 disease evolution and outcomes.
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spelling pubmed-83256222021-08-02 Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated? Soldevila, Berta Puig-Domingo, Manel Marazuela, Mónica Rev Endocr Metab Disord Article Although SARS-CoV-2 viral attacks starts by the interaction of spike protein (S Protein) to ACE2 receptor located at the cell surface of respiratory tract and digestive system cells, different endocrine targets, endocrine organs and metabolic conditions are of fundamental relevance for understanding disease progression and special outcomes, in particular those of fatal consequences for the patient. During pandemic, moreover, a specific phenotype of COVID-19 metabolic patient has been described, characterized by being at particular risk of worse outcomes. In the present paper we describe the mechanism of viral interaction with endocrine organs, emphasizing the specific endocrine molecules of particular relevance explaining COVID-19 disease evolution and outcomes. Springer US 2021-07-31 2022 /pmc/articles/PMC8325622/ /pubmed/34333732 http://dx.doi.org/10.1007/s11154-021-09678-6 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Soldevila, Berta
Puig-Domingo, Manel
Marazuela, Mónica
Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?
title Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?
title_full Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?
title_fullStr Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?
title_full_unstemmed Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?
title_short Basic mechanisms of SARS-CoV-2 infection. What endocrine systems could be implicated?
title_sort basic mechanisms of sars-cov-2 infection. what endocrine systems could be implicated?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325622/
https://www.ncbi.nlm.nih.gov/pubmed/34333732
http://dx.doi.org/10.1007/s11154-021-09678-6
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