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A single cell death is disruptive to spontaneous Ca(2+) activity in astrocytes

Astrocytes in the brain are rapidly recruited to sites of injury where they phagocytose damaged material and take up neurotransmitters and ions to avoid the spreading of damaging molecules. In this study we investigate the calcium (Ca(2+)) response in astrocytes to nearby cell death. To induce cell...

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Detalles Bibliográficos
Autores principales: Gomez-Godinez, Veronica, Li, Huayan, Kuang, Yixuan, Liu, Changchen, Shi, Linda, Berns, Michael W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364045/
https://www.ncbi.nlm.nih.gov/pubmed/35966204
http://dx.doi.org/10.3389/fncel.2022.945737
Descripción
Sumario:Astrocytes in the brain are rapidly recruited to sites of injury where they phagocytose damaged material and take up neurotransmitters and ions to avoid the spreading of damaging molecules. In this study we investigate the calcium (Ca(2+)) response in astrocytes to nearby cell death. To induce cell death in a nearby cell we utilized a laser nanosurgery system to photolyze a selected cell from an established astrocyte cell line (Ast1). Our results show that the lysis of a nearby cell is disruptive to surrounding cells' Ca(2+) activity. Additionally, astrocytes exhibit a Ca(2+) transient in response to cell death which differs from the spontaneous oscillations occurring in astrocytes prior to cell lysis. We show that the primary source of the Ca(2+) transient is the endoplasmic reticulum.