2021
DOI: 10.1016/j.snb.2021.130656
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A unique fluorescent probe for visualization of cell death via its subcellular immigration from lysosomes to nucleus

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Cited by 9 publications
(6 citation statements)
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“…Further, the process of drug-induced cell death was assessed by PNE-Lyso . Rotenone, as a toxin, was used to stimulate cell death . In the cells incubated with rotenone, the fluorescence of PNE-Lyso experienced a ratiometric change between red and yellow channels, and the red fluorescence of PNE-Lyso completely disappeared when the cells were incubated with rotenone for 12 h (Figure S21), indicating that rotenone induced cell death.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Further, the process of drug-induced cell death was assessed by PNE-Lyso . Rotenone, as a toxin, was used to stimulate cell death . In the cells incubated with rotenone, the fluorescence of PNE-Lyso experienced a ratiometric change between red and yellow channels, and the red fluorescence of PNE-Lyso completely disappeared when the cells were incubated with rotenone for 12 h (Figure S21), indicating that rotenone induced cell death.…”
Section: Resultsmentioning
confidence: 99%
“…Rotenone, as a toxin, was used to stimulate cell death. 44 In the cells incubated with rotenone, the fluorescence of PNE-Lyso experienced a ratiometric change between red and yellow channels, and the red fluorescence of PNE-Lyso completely disappeared when the cells were incubated with rotenone for 12 h (Figure S21), indicating that rotenone induced cell death. Continuing to extend the incubation time, the number of granular lysosomes gradually decreased and the morphology became blurred, resulting in that the yellow fluorescence of PNE-Lyso was distributed in the cytoplasm (Figure 7g).…”
Section: Design Strategy and Study Of Spectra Of Pohmentioning
confidence: 99%
“…Benefitting from the overexpressed esterase in cancer cells, TPE-QC could be efficiently activated in cancer cells rather than in normal cells, resulting in enhanced anticancer potency. Lin’s group synthesized a fluorescent probe, LN-2 ( 64 , Scheme 7 ), to visualize cell death based on its subcellular immigration from lysosomes towards the nucleus by regulating the binding affinity of the probe to lysosomes and DNA [ 179 ]. LN-2 was successfully used to display cell death induced by hydrogen peroxide and apoptosis induced by rotenone.…”
Section: Design Of Molecular Probes For Organelle-targeted Cell Imagingmentioning
confidence: 99%
“…It is well known that autophagy and apoptosis are lysosome-dependent pathophysiological processes, which would in turn affect lysosomal properties. Lysosomal pH is significantly decreased during autophagy but evidently increased during apoptosis. By these facts, in this work, a versatile single fluorescent probe for the ratiometric and discriminative visualization of autophagy and apoptosis based on the aggregation/monomer principle has been developed. As illustrated in Scheme a, the probe could simultaneously and separately target lysosomes and RNA with different fluorescent colors.…”
Section: Introductionmentioning
confidence: 99%