Article Text

Download PDFPDF

Molecular impact of graphene oxide with different shape dimension on human immune cells
  1. Marco Orecchioni1,
  2. Dhifaf Jasim2,
  3. Mario Pescatori1,
  4. Francesco Sgarrella1,
  5. Davide Bedognetti3,
  6. Alberto Bianco4,
  7. Kostas Kostarelos2 and
  8. Lucia Delogu1
  1. Aff1 grid.11450.310000000120979138University of Sassari Sassari Italy
  2. Aff2 grid.5379.80000000121662407Faculty of Medical & Human SciencesUniversity of Manchester Manchester UK
  3. Aff3 grid.467063.00000000403974222Sidra Medical and Research Center Doha Qatar
  4. Aff4 grid.4444.00000 0001 2112 9282CNRSInstitute de Biologie Moléculaire et Cellulaire Strasbourg France

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Meeting abstracts

In the last few years, there has been enormous interest in graphene oxide (GO) for its wide variety of applications[1]. However, for any medical application, the immune system-impact of GO still remain to be fully understood. Moreover, the modulation of immune cells mediated by nanomaterials could be interesting also in immunotheraphy applications[2]. Indeed, nanomaterials and more in general nanotechnology can enhance the efficacy of immunostimulatory small molecules and biologics by altering their co-localization, biodistribution, and release kinetics[3].

Following these aims we focused on the molecular effects of two GOs, different for lateral size dimensions, on human peripheral blood mononuclear cells (PBMCs). GOs were fully characterized then, we performed a wide range of standard assays looking at cell viability, cell activation and multiple cytokines secretion. We characterized the molecular impact of GOs on 84 genes immune-response-related. Additionally, a whole genome analysis was conducted on T cells and monocytes as representative of the innate and adaptive immune responses. In Figure 1 TEM and AFM characterization of GO-Small (140 nm) and GO-Large (4mm). We did not detect any toxicity in GO PBMCs treated samples. The 84 gene expression analysis evidenced a clear dimension-dependent impact of GOs on cell activation (Figure 2). In particular, the GO-Small modulated 16 genes (Fold Regulation >4) compared to only 5 of GO-Large (in red in Figure 2 C). Action confirmed also by cytokine analysis (Figure 2 D). These evidences were also confirmed by microarray analysis on T and monocytes cell lines. GO-Small impact the immune cell activation, underlined by the over expression of many pathways such as leukocyte chemotaxis pathway (Figure 3), genes such as CXCL10 ligand pathway and CXCR3 receptor (Figure 3, red box). Moreover, we found a strong action on cell metabolism with a down-regulation on energetic pathways such as oxidative-phosphorylation pathway in both cell types (data not shown). Our work represents a comprehensive molecular-characterization of different sized GOs on immune cells giving crucial information for the chemical and physical design of graphene for biomedical applications i.e. as a new possible drug delivery systems and nanoimmunotherapy tools.



  1. 1.
  2. 2.
  3. 3.