A journey into the retina: Müller Glia commanding survival and death

Müller Glial Cells (MGCs) are known to participate actively in retinal development and to contribute to homeostasis through many intracellular mechanisms. As there are no homologous cells in other neuronal tissues, it is certain that retinal health depends on MGCs. These macroglial cells are located...

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Detalles Bibliográficos
Autores: Subirada Caldarone, Paula Virginia, Paz, Maria Constanza, Ridano, Magali Evelin, Lorenc, Valeria Erika, Vaglienti, María Victoria, Barcelona, Pablo Federico, Luna, José Domingo, Sanchez, Maria Cecilia
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2018
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/158596
Acceso en línea:http://hdl.handle.net/11336/158596
Access Level:acceso abierto
Palabra clave:DIABETIC RETINOPATHY
GLIOSIS
INFLAMMATION
MULLER GLIAL CELLS
TROPHIC FACTORS
https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
Descripción
Sumario:Müller Glial Cells (MGCs) are known to participate actively in retinal development and to contribute to homeostasis through many intracellular mechanisms. As there are no homologous cells in other neuronal tissues, it is certain that retinal health depends on MGCs. These macroglial cells are located at the centre of the columnar subunit and have a great ability to interact with neurons, astrocytes, microglia and endothelial cells in order to modulate different events. Several investigations have focused their attention on the role of MGCs in diabetic retinopathy, a progressive pathology where several insults coexist. As expected, data suggest that MGCs display different responses according to the severity of the stimulus, and therefore trigger distinct events throughout the course of the disease. Here, we describe physiological functions of MGCs and their participation in inflammation, gliosis, synthesis and secretion of trophic and antioxidant factors in the diabetic retina. We invite the reader to consider the protective/deleterious role of MGCs in the early and late stages of the disease. In light of the results, we open up the discussion around and ask the question: is it possible that the modulation of a single cell type could improve or even re-establish retinal function after an injury?