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Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability?
Nicotinamide adenine dinucleotide (NAD(+)) is a fundamental molecule in the regulation of energy metabolism, representing both a coenzyme and a substrate for different NAD(+) degrading enzymes. Among these enzymes, CD38 can be seen under two perspectives: as the enzyme synthesizing Ca(2+)-mobilizing...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8624254/ https://www.ncbi.nlm.nih.gov/pubmed/34835990 http://dx.doi.org/10.3390/nu13113734 |
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author | Benzi, Andrea Grozio, Alessia Spinelli, Sonia Sturla, Laura Guse, Andreas H. De Flora, Antonio Zocchi, Elena Heeren, Joerg Bruzzone, Santina |
author_facet | Benzi, Andrea Grozio, Alessia Spinelli, Sonia Sturla, Laura Guse, Andreas H. De Flora, Antonio Zocchi, Elena Heeren, Joerg Bruzzone, Santina |
author_sort | Benzi, Andrea |
collection | PubMed |
description | Nicotinamide adenine dinucleotide (NAD(+)) is a fundamental molecule in the regulation of energy metabolism, representing both a coenzyme and a substrate for different NAD(+) degrading enzymes. Among these enzymes, CD38 can be seen under two perspectives: as the enzyme synthesizing Ca(2+)-mobilizing second messenger, starting from NAD(+), and as the major NAD(+)-consumer, to be inhibited to increase NAD(+) levels. Indeed, the regulation of NAD(+) availability is a key event during different processes. In this review, we examine the recent studies related to the modulation of CD38 expression and activity, and the consequent changes in NAD(P)(H), in adipose tissue, during inflammation and cold-induced thermogenesis. |
format | Online Article Text |
id | pubmed-8624254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86242542021-11-27 Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? Benzi, Andrea Grozio, Alessia Spinelli, Sonia Sturla, Laura Guse, Andreas H. De Flora, Antonio Zocchi, Elena Heeren, Joerg Bruzzone, Santina Nutrients Review Nicotinamide adenine dinucleotide (NAD(+)) is a fundamental molecule in the regulation of energy metabolism, representing both a coenzyme and a substrate for different NAD(+) degrading enzymes. Among these enzymes, CD38 can be seen under two perspectives: as the enzyme synthesizing Ca(2+)-mobilizing second messenger, starting from NAD(+), and as the major NAD(+)-consumer, to be inhibited to increase NAD(+) levels. Indeed, the regulation of NAD(+) availability is a key event during different processes. In this review, we examine the recent studies related to the modulation of CD38 expression and activity, and the consequent changes in NAD(P)(H), in adipose tissue, during inflammation and cold-induced thermogenesis. MDPI 2021-10-23 /pmc/articles/PMC8624254/ /pubmed/34835990 http://dx.doi.org/10.3390/nu13113734 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Benzi, Andrea Grozio, Alessia Spinelli, Sonia Sturla, Laura Guse, Andreas H. De Flora, Antonio Zocchi, Elena Heeren, Joerg Bruzzone, Santina Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? |
title | Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? |
title_full | Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? |
title_fullStr | Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? |
title_full_unstemmed | Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? |
title_short | Role of CD38 in Adipose Tissue: Tuning Coenzyme Availability? |
title_sort | role of cd38 in adipose tissue: tuning coenzyme availability? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8624254/ https://www.ncbi.nlm.nih.gov/pubmed/34835990 http://dx.doi.org/10.3390/nu13113734 |
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