RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage
RAGE is a multiligand receptor able to bind advanced glycation end-products (AGEs), amphoterin, calgranulins, and amyloid-beta peptides, identified in many tissues and cells, including neurons. RAGE stimulation induces the generation of reactive oxygen species (ROS) mainly through the activity of NA...
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doaj-4fbb31d9044843478abdad98aab04f8b2020-11-24T21:01:29ZengHindawi LimitedOxidative Medicine and Cellular Longevity1942-09001942-09942016-01-01201610.1155/2016/93486519348651RAGE Expression and ROS Generation in Neurons: Differentiation versus DamageS. Piras0A. L. Furfaro1C. Domenicotti2N. Traverso3U. M. Marinari4M. A. Pronzato5M. Nitti6Department of Experimental Medicine, University of Genoa, Via L.B. Alberti 2, 16132 Genoa, ItalyGiannina Gaslini Institute, Via Gerolamo Gaslini 5, 16147 Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Via L.B. Alberti 2, 16132 Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Via L.B. Alberti 2, 16132 Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Via L.B. Alberti 2, 16132 Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Via L.B. Alberti 2, 16132 Genoa, ItalyDepartment of Experimental Medicine, University of Genoa, Via L.B. Alberti 2, 16132 Genoa, ItalyRAGE is a multiligand receptor able to bind advanced glycation end-products (AGEs), amphoterin, calgranulins, and amyloid-beta peptides, identified in many tissues and cells, including neurons. RAGE stimulation induces the generation of reactive oxygen species (ROS) mainly through the activity of NADPH oxidases. In neuronal cells, RAGE-induced ROS generation is able to favor cell survival and differentiation or to induce death through the imbalance of redox state. The dual nature of RAGE signaling in neurons depends not only on the intensity of RAGE activation but also on the ability of RAGE-bearing cells to adapt to ROS generation. In this review we highlight these aspects of RAGE signaling regulation in neuronal cells.http://dx.doi.org/10.1155/2016/9348651 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
S. Piras A. L. Furfaro C. Domenicotti N. Traverso U. M. Marinari M. A. Pronzato M. Nitti |
spellingShingle |
S. Piras A. L. Furfaro C. Domenicotti N. Traverso U. M. Marinari M. A. Pronzato M. Nitti RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage Oxidative Medicine and Cellular Longevity |
author_facet |
S. Piras A. L. Furfaro C. Domenicotti N. Traverso U. M. Marinari M. A. Pronzato M. Nitti |
author_sort |
S. Piras |
title |
RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage |
title_short |
RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage |
title_full |
RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage |
title_fullStr |
RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage |
title_full_unstemmed |
RAGE Expression and ROS Generation in Neurons: Differentiation versus Damage |
title_sort |
rage expression and ros generation in neurons: differentiation versus damage |
publisher |
Hindawi Limited |
series |
Oxidative Medicine and Cellular Longevity |
issn |
1942-0900 1942-0994 |
publishDate |
2016-01-01 |
description |
RAGE is a multiligand receptor able to bind advanced glycation end-products (AGEs), amphoterin, calgranulins, and amyloid-beta peptides, identified in many tissues and cells, including neurons. RAGE stimulation induces the generation of reactive oxygen species (ROS) mainly through the activity of NADPH oxidases. In neuronal cells, RAGE-induced ROS generation is able to favor cell survival and differentiation or to induce death through the imbalance of redox state. The dual nature of RAGE signaling in neurons depends not only on the intensity of RAGE activation but also on the ability of RAGE-bearing cells to adapt to ROS generation. In this review we highlight these aspects of RAGE signaling regulation in neuronal cells. |
url |
http://dx.doi.org/10.1155/2016/9348651 |
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1716777857012727808 |