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Construction of a mitochondrial targeted H2O2 fluorescence probe with a large Stokes shift and its application in bacterial infection
Macrophages are crucial innate immune system cells that have the ability to generate large amounts of H2O2 in the cytoplasm to combat germs. Macrophage mitochondria also produce H2O2 to participate in the antimicrobial response when infected by bacteria. However, visualization of H2O2 production in...
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Published in: | Dyes and pigments 2024-06, Vol.225, p.112103, Article 112103 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Macrophages are crucial innate immune system cells that have the ability to generate large amounts of H2O2 in the cytoplasm to combat germs. Macrophage mitochondria also produce H2O2 to participate in the antimicrobial response when infected by bacteria. However, visualization of H2O2 production in the mitochondria of bacterially infected macrophages is extremely challenging due to the lack of appropriate research methods. Here, by developing a new mitochondrial-targeting fluorescent H2O2 probe, combined with confocal fluorescence imaging, we report for the first time that H2O2 production in the mitochondria of bacterially infected macrophages (Raw264.7 cells) was visualized with a fluorescent probe. In addition, the developed probe has accurate mitochondrial targeting ability, large Stokes shift, fast response capability, high selectivity and sensitivity (detection limit of 4.346 × 10−7 M), and the probe can be used to detect H2O2 in living cells and zebrafish. Therefore, this work is expected to be used to further reveal the biological function of H2O2 in subcellular mitochondria.
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•H2O2 production by macrophages during bacterial infection can be detected.•Has a large Stokes shift (about 235 nm).•Has excellent selectivity and anti-interference ability to H2O2 detection.•Imaging exogenous and endogenous H2O2 in living cells and zebrafish. |
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ISSN: | 0143-7208 1873-3743 |
DOI: | 10.1016/j.dyepig.2024.112103 |