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Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells

Lysosomes are the catabolic center of the cell. Limitations of many lysosomal tracers include low specificity and lack of reliable physiological readouts for changes in growth factor-regulated lysosomal activity. The imaging-based protocols described here provide insights at the cellular level to qu...

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Detalles Bibliográficos
Autores principales: Albrecht, L.V., Tejeda-Muñoz, N., De Robertis, E.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757114/
https://www.ncbi.nlm.nih.gov/pubmed/33377026
http://dx.doi.org/10.1016/j.xpro.2020.100132
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author Albrecht, L.V.
Tejeda-Muñoz, N.
De Robertis, E.M.
author_facet Albrecht, L.V.
Tejeda-Muñoz, N.
De Robertis, E.M.
author_sort Albrecht, L.V.
collection PubMed
description Lysosomes are the catabolic center of the cell. Limitations of many lysosomal tracers include low specificity and lack of reliable physiological readouts for changes in growth factor-regulated lysosomal activity. The imaging-based protocols described here provide insights at the cellular level to quantify functions essential to lysosomal biology, including β-glucosidase enzymatic cleavage, active Cathepsin D, and pH regulation in real time. These optimized protocols, applied in different cell types and pathophysiologic contexts, provide useful tools to study lysosome function in cultured living cells. For complete details on the use and execution of this protocol, please refer to Albrecht et al. (2020).
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spelling pubmed-77571142020-12-28 Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells Albrecht, L.V. Tejeda-Muñoz, N. De Robertis, E.M. STAR Protoc Protocol Lysosomes are the catabolic center of the cell. Limitations of many lysosomal tracers include low specificity and lack of reliable physiological readouts for changes in growth factor-regulated lysosomal activity. The imaging-based protocols described here provide insights at the cellular level to quantify functions essential to lysosomal biology, including β-glucosidase enzymatic cleavage, active Cathepsin D, and pH regulation in real time. These optimized protocols, applied in different cell types and pathophysiologic contexts, provide useful tools to study lysosome function in cultured living cells. For complete details on the use and execution of this protocol, please refer to Albrecht et al. (2020). Elsevier 2020-10-17 /pmc/articles/PMC7757114/ /pubmed/33377026 http://dx.doi.org/10.1016/j.xpro.2020.100132 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Albrecht, L.V.
Tejeda-Muñoz, N.
De Robertis, E.M.
Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells
title Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells
title_full Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells
title_fullStr Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells
title_full_unstemmed Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells
title_short Protocol for Probing Regulated Lysosomal Activity and Function in Living Cells
title_sort protocol for probing regulated lysosomal activity and function in living cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757114/
https://www.ncbi.nlm.nih.gov/pubmed/33377026
http://dx.doi.org/10.1016/j.xpro.2020.100132
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