Literature DB >> 18161533

Novel lipophilic tracking dyes for monitoring cell proliferation.

Joseph D Tario1, Brian D Gray, Stephen S Wallace, Katharine A Muirhead, Betsy M Ohlsson-Wilhelm, Paul K Wallace.   

Abstract

The advent of contemporary digital instrumentation has enhanced both the potential and the complexity of flow cytometric experiments, allowing for the detailed dissection of immune cell subsets and their functions. The use of cell tracking labels such as PKH26 and CFSE has been important in observing such cellular functions, but their visible emission characteristics have limited the design of such analyses. As the demand for multiparametric flow cytometry intensifies, it will become increasingly important to utilize a broader range of cell tracking reagents to optimize the measurement of fluorescence signals and to provide flexibility in the use of commercially available fluorochrome - antibody combinations. We report on the evaluation of three lipophilic membrane dyes, CellVue Lavender, CellVue Plum and CellVue NIR780; with fluorescence emissions in the violet, far-red and near infrared wavelength regions, respectively. These reagents are similar to established tracking dyes such as PKH26 and CFSE in terms of staining procedure, membrane stability, optimal concentration, and lack of effect on cellular proliferation. The CellVue dyes however, exhibit different spectral characteristics than existing tracking compounds, and capitalize upon the increased number of lasers incorporated into commercially available instrumentation; thus permitting measurement of labeled populations in underexploited regions of the spectrum.

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Year:  2007        PMID: 18161533     DOI: 10.1080/08820130701712933

Source DB:  PubMed          Journal:  Immunol Invest        ISSN: 0882-0139            Impact factor:   3.657


  8 in total

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Journal:  J Virol       Date:  2013-10-02       Impact factor: 5.103

2.  Optimized staining and proliferation modeling methods for cell division monitoring using cell tracking dyes.

Authors:  Joseph D Tario; Kristen Humphrey; Andrew D Bantly; Katharine A Muirhead; Jonni S Moore; Paul K Wallace
Journal:  J Vis Exp       Date:  2012-12-13       Impact factor: 1.355

3.  Tracking immune cell proliferation and cytotoxic potential using flow cytometry.

Authors:  Joseph D Tario; Katharine A Muirhead; Dalin Pan; Mark E Munson; Paul K Wallace
Journal:  Methods Mol Biol       Date:  2011

4.  Simultaneous analysis of p53 protein expression and cell proliferation in irradiated human lymphocytes by flow cytometry.

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Journal:  Dose Response       Date:  2013-08-27       Impact factor: 2.658

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Authors:  Daniel L J Thorek; Patricia Y Tsao; Vaishali Arora; Lanlan Zhou; Robert A Eisenberg; Andrew Tsourkas
Journal:  PLoS One       Date:  2010-05-17       Impact factor: 3.240

6.  Enhanced cellular uptake of albumin-based lyophilisomes when functionalized with cell-penetrating peptide TAT in HeLa cells.

Authors:  Etienne van Bracht; Luuk R M Versteegden; Sarah Stolle; Wouter P R Verdurmen; Rob Woestenenk; René Raavé; Theo Hafmans; Egbert Oosterwijk; Roland Brock; Toin H van Kuppevelt; Willeke F Daamen
Journal:  PLoS One       Date:  2014-11-04       Impact factor: 3.240

7.  The Positive Impact of Donor Bone Marrow Cells Transplantation into Immunoprivileged Compartments on the Survival of Vascularized Skin Allografts.

Authors:  Arkadiusz Jundziłł; Aleksandra Klimczak; Erhan Sonmez; Grzegorz Brzezicki; Maria Siemionow
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2021-10-11       Impact factor: 4.291

8.  Monitoring Cell Proliferation by Dye Dilution: Considerations for Probe Selection.

Authors:  Joseph D Tario; Alexis N Conway; Katharine A Muirhead; Paul K Wallace
Journal:  Methods Mol Biol       Date:  2018
  8 in total

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