Lc3-gfp Marker

An LC3-GFP marker is a fluorescent reporter used to visualize autophagy, the lysosome-dependent process that degrades and recycles intracellular components, making it valuable for studying how cancer cells survive cellular stress. In this system, green fluorescent protein (GFP) is fused to LC3; during autophagy, LC3 is lipidated and recruited to forming autophagosomal membranes, producing detectable fluorescent puncta. Researchers monitor changes in diffuse fluorescence and puncta formation to assess autophagy-related responses to nutrient deprivation, anticancer treatments, or genetic manipulation. Because autophagy can support or limit tumor progression, LC3-GFP imaging helps investigate cancer biology and evaluate potential therapeutic strategies.

Lc3-gfp Marker - Related Videos

Research

JoVE Journal - Biology
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Assessing Autophagic Flux by Measuring LC3, p62, and LAMP1 Co-localization Using Multispectral Imaging Flow Cytometry

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Cited by 94 •

2017

Here, multispectral imaging flow cytometry with an analytical feature that compares bright detail images of 3 autophagy markers and quantifies their co-localization, along with LC3 spot counting, was used to measure autophagy in an objective, quantitative, and statistically robust manner.

Research

JoVE Journal - Biochemistry

Evaluation of LC3-II Release via Extracellular Vesicles in Relation to the Accumulation of Intracellular LC3-positive Vesicles

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Cited by 7 •

2024

Here, we present the methodology for concisely assessing autophagosome marker LC3-II levels in extracellular vesicles (EVs) by immunoblotting. Analysis for LC3-II levels in EVs, autolysosome formation, and omegasome formation suggests the new role of STX6 in the release of LC3-II-positive EVs when autophagosome-lysosome fusion is inhibited.

Imaging the Intracellular Trafficking of APP with Photoactivatable GFP

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Cited by 6 •

2015

While the transport of cell surface proteins is relatively easily studied, visualizing the trafficking of intracellular proteins is much more difficult. Here, we use constructs incorporating photoactivatable GFP and demonstrate a method to accurately follow the amyloid precursor protein from the Golgi apparatus to down-stream compartments and follow its clearance.

Research

JoVE Journal - Neuroscience
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Electrophysiological Characterization of GFP-Expressing Cell Populations in the Intact Retina

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Cited by 5 •

2011

This article depicts the recording of individual cells from fluorescently tagged neuronal populations in the intact mouse retina. By using two-photon infrared excitation transgenetically labeled cells were targeted for patch-clamp recording to study their light responses, receptive field properties, and morphology.

Tracking Cells in GFP-transgenic Zebrafish Using the Photoconvertible PSmOrange System

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Cited by 2 •

2016

We established the photoconvertible PSmOrange system as a powerful, straight-forward and cost inexpensive tool for in vivo cell tracking in GFP transgenic backgrounds. This protocol describes its application in the zebrafish model system.

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