001     167779
005     20240229123236.0
024 7 _ |a 10.21769/BioProtoc.3737
|2 doi
024 7 _ |a pmid:33659398
|2 pmid
024 7 _ |a pmc:PMC7842666
|2 pmc
024 7 _ |a altmetric:101347114
|2 altmetric
037 _ _ |a DKFZ-2021-00541
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Bode, Kevin
|0 P:(DE-He78)322352fbba1747192994bd6eff973bd8
|b 0
|e First author
|u dkfz
245 _ _ |a Flow-cytometric Detection of Low-level Reactive Oxygen Species in Cell Lines and Primary Immune Cells.
260 _ _ |a Sunnyvale, CA
|c 2020
|b bio-protocol.org
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
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|s 1615279623_28694
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
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500 _ _ |a #EA:D030#LA:D030#
520 _ _ |a Depending on its concentration and cellular origin the production of reactive oxygen species (ROS) in the organism serves a variety of functions. While high concentrations during an oxidative burst are used to fight pathogens, low to moderate amounts of ROS act as signaling molecules important for several physiological processes such as regulation of immune responses. The ROS-sensitive dye 2',7'-dichlorodihydrofluorescein diacetate (H2DCFDA) is an inexpensive and well-established tool for measuring intracellular ROS levels. However, it needs to be carefully controlled to be able to draw firm conclusions on the nature of ROS species produced and the cellular source of ROS generation such as the enzyme complex NADPH-oxidase 2 (NOX-2). In this protocol, a robust method to determine low intracellular ROS production using H2DCFDA was validated by several ROS-specific as well as NOX-2-specific inhibitors. Cells were treated with inhibitors or control substances prior to treatment with the ROS-inducer of interest. H2DCFDA was added only for the last 30 min of the treatment schedule. To terminate its conversion, we used a ROS-specific inhibitor until analysis by flow cytometry within the FITC-channel (Ex: 488 nm/Em: 519 nm). In summary, this protocol allows the detection of signaling-relevant intracellular ROS production in cell lines and primary immune cells (e.g., Mono Mac 6 cells and Bone marrow-derived dendritic cells, respectively). Using this method in combination with specific inhibitors, we were able to validate even exceptionally low amounts of ROS produced by NOX-2 and relevant for immune-regulatory signaling.
536 _ _ |a 314 - Tumor immunology (POF3-314)
|0 G:(DE-HGF)POF3-314
|c POF3-314
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Bone Marrow-derived Dendritic Cells (BMDCs)
|2 Other
650 _ 7 |a Jurkat T cells
|2 Other
650 _ 7 |a Mono Mac 6 (MM6) cells
|2 Other
650 _ 7 |a NADPH-oxidase 2 (NOX-2)
|2 Other
650 _ 7 |a Reactive Oxygen Species (ROS)
|2 Other
700 1 _ |a Link, Corinna
|0 P:(DE-He78)816f10fe44243f27b2b9a15d421dd186
|b 1
|u dkfz
700 1 _ |a Krammer, Peter H
|0 P:(DE-He78)92492c6eae05ee58973fc142c9201e3d
|b 2
|u dkfz
700 1 _ |a Weyd, Heiko
|0 P:(DE-He78)4dca42511637e2f9d25519745fa3c697
|b 3
|e Last author
|u dkfz
773 _ _ |a 10.21769/BioProtoc.3737
|g Vol. 10, no. 17
|0 PERI:(DE-600)2833269-6
|n 17
|p e3737
|t Bio-protocol
|v 10
|y 2020
|x 2331-8325
909 C O |o oai:inrepo02.dkfz.de:167779
|p VDB
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
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|b 0
|6 P:(DE-He78)322352fbba1747192994bd6eff973bd8
910 1 _ |a Deutsches Krebsforschungszentrum
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910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
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|b 2
|6 P:(DE-He78)92492c6eae05ee58973fc142c9201e3d
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
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|b 3
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913 1 _ |a DE-HGF
|b Gesundheit
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|v Tumor immunology
|x 0
913 2 _ |a DE-HGF
|b Gesundheit
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|v Immunologie und Krebs
|x 0
914 1 _ |y 2020
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
920 1 _ |0 I:(DE-He78)D030-20160331
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|l Immungenetik
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)D030-20160331
980 _ _ |a UNRESTRICTED


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