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Technology Report

Raman microspectroscopy detects epigenetic modifications in living Jurkat leukemic cells

    Mathilde Poplineau

    Unité MEDyC, UMR URCA CNRS 6237, IFR53, Faculté de Pharmacie, Université de Reims, 1 avenue du Maréchal Juin, 51096 Reims, France

    These authors contributed equally

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    , ,
    Teddy Happillon

    Unité MEDyC, UMR URCA CNRS 6237, IFR53, Faculté de Pharmacie, Université de Reims, 1 avenue du Maréchal Juin, 51096 Reims, France

    ,
    Jean Dufer

    Unité MEDyC, UMR URCA CNRS 6237, IFR53, Faculté de Pharmacie, Université de Reims, 1 avenue du Maréchal Juin, 51096 Reims, France

    ,
    Michel Manfait

    Unité MEDyC, UMR URCA CNRS 6237, IFR53, Faculté de Pharmacie, Université de Reims, 1 avenue du Maréchal Juin, 51096 Reims, France

    ,
    Philippe Bernard

    Université de Reims Champagne-Ardenne, Laboratoire de Dermatologie, UMR URCA CNRS 6237, IFR53, Faculté de médecine, Reims, France

    ,
    Olivier Piot

    Unité MEDyC, UMR URCA CNRS 6237, IFR53, Faculté de Pharmacie, Université de Reims, 1 avenue du Maréchal Juin, 51096 Reims, France

    &
    Frank Antonicelli

    Université de Reims Champagne-Ardenne, Laboratoire de Dermatologie, UMR URCA CNRS 6237, IFR53, Faculté de médecine, Reims, France

    Published Online:https://doi.org/10.2217/epi.11.102

    Aims: Classical biochemical and molecular methods for discerning cells with epigenetic modifications are often biologically perturbing or even destructive. We wondered whether the noninvasive laser tweezer Raman spectroscopy technique allowed the discrimination of single living human cells undergoing epigenetic modifications. Materials & methods: Human Jurkat leukemic cells were treated with inhibitors of histone deacetylases (trichostatin A and MS-275). Epigenetic changes were monitored through histone electrophoresis, nuclear image cytometry and laser tweezer Raman spectroscopy. Results: Treatment of Jurkat cells with histone deacetylase inhibitors increased histone acetylation and induced chromatin organization changes. Characteristic vibrations, issued from laser tweezer Raman spectroscopy analyses, mostly assigned to DNA and proteins allowed discerning histone deacetylase inhibitor-treated cells from control with high confidence. Statistical processing of laser tweezer Raman spectroscopy data led to the definition of specific biomolecular fingerprints of each cell group. Conclusion: This original study shows that laser tweezer Raman spectroscopy is a label-free rapid tool to identify living cells that underwent epigenetic changes.

    Papers of special note have been highlighted as: ▪ of interest ▪▪ of considerable interest

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