2017
DOI: 10.1038/s41598-017-08723-2
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Pre-culture Sudan Black B treatment suppresses autofluorescence signals emitted from polymer tissue scaffolds

Abstract: In tissue engineering, autofluorescence of polymer scaffolds often lowers the image contrast, making it difficult to examine cells and subcellular structures. Treating the scaffold materials with Sudan Black B (SBB) after cell fixation can effectively suppress autofluorescence, but this approach is not conducive to live cell imaging. Post-culture SBB treatment also disrupts intracellular structures and leads to reduced fluorescence intensity of the targets of interest. In this study, we introduce pre-culture S… Show more

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Cited by 33 publications
(39 citation statements)
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References 42 publications
(36 reference statements)
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“…This is a quenching compound commonly used in lipid histochemistry to better visualize biological structure. Using a concentration of 0.3% ( w / v ) SB in ethanol that was previously proven to be not toxic and to successfully cancel background fluorescence of polymeric scaffolds (Qi et al, 2017), it was possible to image the live and dead cells after 10 days in culture on most of the samples.…”
Section: Resultsmentioning
confidence: 99%
“…This is a quenching compound commonly used in lipid histochemistry to better visualize biological structure. Using a concentration of 0.3% ( w / v ) SB in ethanol that was previously proven to be not toxic and to successfully cancel background fluorescence of polymeric scaffolds (Qi et al, 2017), it was possible to image the live and dead cells after 10 days in culture on most of the samples.…”
Section: Resultsmentioning
confidence: 99%
“…The plasmid DNA of the resulting fusion construct and p 35S:GFP control were separately introduced into wheat protoplasts by polyethylene glycol (PEG) 4000 or white onion epidermal cells using biolistic bombardment as described previously (Zhang et al , 2007). After incubation at 25 °C for 20 h, GFP signals were observed and photographed (Qi et al , 2017) using a confocal laser scanning microscope (Zeiss LSM 700, Germany) with a Fluor ×10/0.50 M27 objective lens and SP640 filter.…”
Section: Methodsmentioning
confidence: 99%
“…In addition to nonspecific hybrids, autofluorescence and excessive background are issues that can diminish the visibility of true signal and influence the interpretation of the results. Treatment with 0.1% Sudan Black B in 70% ethanol is effective to minimize autofluorescence in sectioned brain tissue as well as cultured cells (Oliveira et al, 2010;Qi et al, 2017). If background signal is an issue, tissues can also be acetylated with 0.3% acetic anhydride in triethanolamine for 5-10 min (Jackson, Herlitze & Hohagen, 2016).…”
Section: Post-hybridization Treatmentsmentioning
confidence: 99%