@article{e59190b132ef491f968b812565756301,
title = "Toward High-Dimensional Single-Cell Analysis of Graphene Oxide Biological Impact: Tracking on Immune Cells by Single-Cell Mass Cytometry",
abstract = "Considering the potential exposure to graphene, the most investigated nanomaterial, the assessment of the impact on human health has become an urgent need. The deep understanding of nanomaterial safety is today possible by high-throughput single-cell technologies. Single-cell mass cytometry (cytometry by time-of flight, CyTOF) shows an unparalleled ability to phenotypically and functionally profile complex cellular systems, in particular related to the immune system, as recently also proved for graphene impact. The next challenge is to track the graphene distribution at the single-cell level. Therefore, graphene oxide (GO) is functionalized with AgInS2 nanocrystals (GO–In), allowing to trace GO immune–cell interactions via the indium (115In) channel. Indium is specifically chosen to avoid overlaps with the commercial panels (>30 immune markers). As a proof of concept, the GO–In CyTOF tracking is performed at the single-cell level on blood immune subpopulations, showing the GO interaction with monocytes and B cells, therefore guiding future immune studies. The proposed approach can be applied not only to the immune safety assessment of the multitude of graphene physical and chemical parameters, but also for graphene applications in neuroscience. Moreover, this approach can be translated to other 2D emerging materials and will likely advance the understanding of their toxicology.",
keywords = "2D materials, CyTOF, biocompatibility, immune cells, safety",
author = "Marco Orecchioni and Valentina Bordoni and Claudia Fuoco and Giacomo Reina and Hazel Lin and Martina Zoccheddu and Acelya Yilmazer and Barbara Zavan and Gianni Cesareni and Davide Bedognetti and Alberto Bianco and Delogu, {Lucia Gemma}",
note = "Funding Information: M.O., V.B., and C.F. contributed equally to this work. This work was partly supported by the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement no. 734381 (CARBO-IMmap), FLAGERA JTC Graphene 2015 (G-IMMUNOMICS project), and the Agence Nationale de la Recherche (ANR) through the LabEx Project Chemistry of Complex Systems (ANR-10-LABX-0026_CSC). The authors gratefully acknowledge the financial support from the EU GRAPHENE Flagship project (no. 785219). The authors wish to thank C. Royer and V. Demais for TEM analyses at the Plateforme Imagerie In Vitro at the INCI (Strasbourg, France). Note: Davide Bedognetti was added as a corresponding author on 26 May 2020 after initial online publication. Funding Information: M.O., V.B., and C.F. contributed equally to this work. This work was partly supported by the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska‐Curie grant agreement no. 734381 (CARBO‐IMmap), FLAGERA JTC Graphene 2015 (G‐IMMUNOMICS project), and the Agence Nationale de la Recherche (ANR) through the LabEx Project Chemistry of Complex Systems (ANR‐10‐LABX‐0026_CSC). The authors gratefully acknowledge the financial support from the EU GRAPHENE Flagship project (no. 785219). The authors wish to thank C. Royer and V. Demais for TEM analyses at the Plateforme Imagerie In Vitro at the INCI (Strasbourg, France). Publisher Copyright: {\textcopyright} 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim",
year = "2020",
month = may,
day = "1",
doi = "10.1002/smll.202000123",
language = "English (US)",
volume = "16",
journal = "Small",
issn = "1613-6810",
publisher = "Wiley-VCH Verlag",
number = "21",
}