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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-...

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Detalles Bibliográficos
Autores principales: Velázquez, Esther, Le Baut Ayuso, Yannick, Blázquez, Enrique, Ruiz-Albusac, Juan Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2022
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
Descripción
Sumario: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.