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Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes
BACKGROUND: Glucagon-like peptide-2 (GLP-2) is an intestinal trophic factor that induces astrocyte proliferation through its own receptor (GLP-2R), but the control of its expression is not well known. OBJECTIVE: To study the effects of glucose and of different mitogenic agents on the control of GLP-...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741749/ https://www.ncbi.nlm.nih.gov/pubmed/36606205 http://dx.doi.org/10.3233/ADR-220043 |
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author | Velázquez, Esther Le Baut Ayuso, Yannick Blázquez, Enrique Ruiz-Albusac, Juan Miguel |
author_facet | Velázquez, Esther Le Baut Ayuso, Yannick Blázquez, Enrique Ruiz-Albusac, Juan Miguel |
author_sort | Velázquez, Esther |
collection | PubMed |
description | BACKGROUND: Glucagon-like peptide-2 (GLP-2) is an intestinal trophic factor that induces astrocyte proliferation through its own receptor (GLP-2R), but the control of its expression is not well known. OBJECTIVE: To study the effects of glucose and of different mitogenic agents on the control of GLP-2R expression in cultured rat astrocytes. METHODS: GLP-2R mRNA content was measured by quantitative RT-PCR. RESULTS: GLP-2R expression was higher in proliferating than in resting cells. The expression was dependent of glucose concentration both in the absence and in the presence of GLP-2. In the presence of a high glucose concentration, GLP-2, PDGF, and PDGF plus GLP-2 presented opposite effects depending on the incubation time. However, insulin, IGF-1, and EGF alone, and plus GLP-2 had no effect. IGF-2, but not IGF-2 plus GLP-2, increased the expression. On the contrary, NGF decreased the GLP-2R expression, but NGF plus GLP-2 increased it even until values similar to those obtained with GLP-2 alone. Interestingly, in the presence of a low glucose concentration, leptin and NPY produced a significant reduction of GLP-2R expression. CONCLUSION: Astrocytes are distributed throughout the brain, where GLP-2 appears to have important functions. Since these cells express the GLP-2R, the results of this study could be considered of interest to advance the knowledge of the role of GLP-2 signaling in the CNS, which should lead a better understanding of the events that occur under normal and pathophysiological conditions. |
format | Online Article Text |
id | pubmed-9741749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-97417492023-01-04 Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes Velázquez, Esther Le Baut Ayuso, Yannick Blázquez, Enrique Ruiz-Albusac, Juan Miguel J Alzheimers Dis Rep Research Article BACKGROUND: Glucagon-like peptide-2 (GLP-2) is an intestinal trophic factor that induces astrocyte proliferation through its own receptor (GLP-2R), but the control of its expression is not well known. OBJECTIVE: To study the effects of glucose and of different mitogenic agents on the control of GLP-2R expression in cultured rat astrocytes. METHODS: GLP-2R mRNA content was measured by quantitative RT-PCR. RESULTS: GLP-2R expression was higher in proliferating than in resting cells. The expression was dependent of glucose concentration both in the absence and in the presence of GLP-2. In the presence of a high glucose concentration, GLP-2, PDGF, and PDGF plus GLP-2 presented opposite effects depending on the incubation time. However, insulin, IGF-1, and EGF alone, and plus GLP-2 had no effect. IGF-2, but not IGF-2 plus GLP-2, increased the expression. On the contrary, NGF decreased the GLP-2R expression, but NGF plus GLP-2 increased it even until values similar to those obtained with GLP-2 alone. Interestingly, in the presence of a low glucose concentration, leptin and NPY produced a significant reduction of GLP-2R expression. CONCLUSION: Astrocytes are distributed throughout the brain, where GLP-2 appears to have important functions. Since these cells express the GLP-2R, the results of this study could be considered of interest to advance the knowledge of the role of GLP-2 signaling in the CNS, which should lead a better understanding of the events that occur under normal and pathophysiological conditions. IOS Press 2022-11-22 /pmc/articles/PMC9741749/ /pubmed/36606205 http://dx.doi.org/10.3233/ADR-220043 Text en © 2022 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Velázquez, Esther Le Baut Ayuso, Yannick Blázquez, Enrique Ruiz-Albusac, Juan Miguel Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes |
title | Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes |
title_full | Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes |
title_fullStr | Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes |
title_full_unstemmed | Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes |
title_short | Glucose and Several Mitogenic Agents Modulate the Glucagon-Like Peptide-2 Receptor Expression in Cultured Rat Astrocytes |
title_sort | glucose and several mitogenic agents modulate the glucagon-like peptide-2 receptor expression in cultured rat astrocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741749/ https://www.ncbi.nlm.nih.gov/pubmed/36606205 http://dx.doi.org/10.3233/ADR-220043 |
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