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Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes
Arginase 2 (ARG2) is a manganese metalloenzyme involved in several tissue specific processes, from physiology to pathophysiology. It is variably expressed in extra-hepatic tissues and is located in the mitochondria. In human pancreatic beta cells, ARG2 is downregulated in type 2 diabetes. The enzyme...
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/PMC8625980/ https://www.ncbi.nlm.nih.gov/pubmed/34829980 http://dx.doi.org/10.3390/ijms222212099 |
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author | Marselli, Lorella Bosi, Emanuele De Luca, Carmela Del Guerra, Silvia Tesi, Marta Suleiman, Mara Marchetti, Piero |
author_facet | Marselli, Lorella Bosi, Emanuele De Luca, Carmela Del Guerra, Silvia Tesi, Marta Suleiman, Mara Marchetti, Piero |
author_sort | Marselli, Lorella |
collection | PubMed |
description | Arginase 2 (ARG2) is a manganese metalloenzyme involved in several tissue specific processes, from physiology to pathophysiology. It is variably expressed in extra-hepatic tissues and is located in the mitochondria. In human pancreatic beta cells, ARG2 is downregulated in type 2 diabetes. The enzyme regulates the synthesis of polyamines, that are involved in pancreas development and regulation of beta cell function. Here, we discuss several features of ARG2 and polyamines, which can be relevant to the pathophysiology of type 2 diabetes. |
format | Online Article Text |
id | pubmed-8625980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86259802021-11-27 Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes Marselli, Lorella Bosi, Emanuele De Luca, Carmela Del Guerra, Silvia Tesi, Marta Suleiman, Mara Marchetti, Piero Int J Mol Sci Review Arginase 2 (ARG2) is a manganese metalloenzyme involved in several tissue specific processes, from physiology to pathophysiology. It is variably expressed in extra-hepatic tissues and is located in the mitochondria. In human pancreatic beta cells, ARG2 is downregulated in type 2 diabetes. The enzyme regulates the synthesis of polyamines, that are involved in pancreas development and regulation of beta cell function. Here, we discuss several features of ARG2 and polyamines, which can be relevant to the pathophysiology of type 2 diabetes. MDPI 2021-11-09 /pmc/articles/PMC8625980/ /pubmed/34829980 http://dx.doi.org/10.3390/ijms222212099 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 Marselli, Lorella Bosi, Emanuele De Luca, Carmela Del Guerra, Silvia Tesi, Marta Suleiman, Mara Marchetti, Piero Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes |
title | Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes |
title_full | Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes |
title_fullStr | Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes |
title_full_unstemmed | Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes |
title_short | Arginase 2 and Polyamines in Human Pancreatic Beta Cells: Possible Role in the Pathogenesis of Type 2 Diabetes |
title_sort | arginase 2 and polyamines in human pancreatic beta cells: possible role in the pathogenesis of type 2 diabetes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625980/ https://www.ncbi.nlm.nih.gov/pubmed/34829980 http://dx.doi.org/10.3390/ijms222212099 |
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