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A protocol to measure lysosomal Zn(2+) release through a genetically encoded Zn(2+) indicator

Intracellular vesicles such as lysosomes contain micromolar to millimolar concentrations of Zn(2+), and disturbing lysosomal Zn(2+) homeostasis via lysosomal Zn(2+) release leads to mitochondria damage and consequent lytic cell death. Methods have been developed to image cellular Zn(2+) dynamics. He...

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Detalles Bibliográficos
Autores principales: Gu, Mingxue, Hu, Meiqin, Minckley, Taylor, Pinchi, Prateeksunder, Xu, Haoxing, Qin, Yan, Du, Wanlu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9189625/
https://www.ncbi.nlm.nih.gov/pubmed/35707683
http://dx.doi.org/10.1016/j.xpro.2022.101453
Descripción
Sumario:Intracellular vesicles such as lysosomes contain micromolar to millimolar concentrations of Zn(2+), and disturbing lysosomal Zn(2+) homeostasis via lysosomal Zn(2+) release leads to mitochondria damage and consequent lytic cell death. Methods have been developed to image cellular Zn(2+) dynamics. Here, we present a protocol using GZnP3, a genetically encoded fluorescent Zn(2+) indicator, to assess lysosomal Zn(2+) release in cultured cells by fluorescence microscopy imaging. For complete details on the use and execution of this protocol, please refer to Du et al. (2021) or Minckley et al. (2019).