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Experimental and computational analyses of calcium dynamics in 22q11.2 deletion model astrocytes.
Maly, Ivan V; Hofmann, Wilma A; Pletnikov, Mikhail V.
Afiliación
  • Maly IV; Department of Physiology and Biophysics, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
  • Hofmann WA; Department of Physiology and Biophysics, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA.
  • Pletnikov MV; Department of Physiology and Biophysics, Jacobs School of Medicine and Biomedical Sciences, State University of New York at Buffalo, Buffalo, NY 14203, USA; Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD 21225, USA. Electronic address: mvpletni@buffalo.edu.
Neurosci Lett ; 783: 136711, 2022 07 13.
Article en En | MEDLINE | ID: mdl-35671915
ABSTRACT
Methods for deriving mechanistic information from intracellular calcium dynamics have largely been applied to neuronal data despite the knowledge of roles of glial cells in behavior, cognition, and psychiatric disorders. Using calcium imaging, computer vision, and Bayesian kinetic inference (BKI), we analyzed calcium dynamics in primary astrocytes derived from control or Df1/+ mice, a model of 22q11.2 deletion (DiGeorge syndrome). Inference of the highest-likelihood molecular kinetic characteristics of intracellular calcium dynamics identified changes in the activity of the sarcoendoplasmic reticulum calcium ATPase (SERCA). Application of a SERCA inhibitor to wild-type astrocytes reproduced the differences detected in Df1/+ astrocytes. Our work reveals the molecular changes driving the calcium kinetics in astrocytes from a 22q11.2 deletion model. BKI can be useful for mechanistically dissecting calcium dynamics in glial cells and formulating and testing hypotheses about underlying molecular mechanisms.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Calcio / Síndrome de DiGeorge Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Neurosci Lett Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Calcio / Síndrome de DiGeorge Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Neurosci Lett Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos