Graphene Oxide Nanosheets Stimulate Ruffling and Shedding of Mammalian Cell Plasma Membranes

Chao Sun, Devin L. Wakefield, Yimo Han, David A. Muller, David A. Holowka, Barbara A. Baird, William R. Dichtel*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

Graphene oxide (GO) has attracted intense interest for use in living systems and environmental applications. GO's compatibility with mammalian cells is sometimes inferred from its low cytotoxicity, but such conclusions ignore non-lethal effects that will influence GO's utility. Here, we used confocal and live-cell fluorescence microscopy, as well as scanning electron microscopy, of rat basophilic leukemia (RBL) cells to demonstrate profound plasma membrane (PM) ruffling and shedding induced by GO. These membrane structures contain immunoglobulin E receptors, are resistant to detergents, and lack detectable fluorescence labeling of F-actin and fibronectin. The formation of these membrane structures correlates with a loss of contact inhibition between RBL cells. We observed similar cellular responses toward GO for NIH-3T3 fibroblast cells and MDA-MB-231 human breast cancer cells. These findings reveal a previously uncharacterized cellular response toward foreign nanomaterials. Membrane ruffling and shedding raise fundamental questions about how GO interacts with the PM, as well as its potential to modulate cellular mechanosensing for tissue engineering, stem cell differentiation, and other biomedical applications.

Original languageEnglish (US)
Pages (from-to)273-286
Number of pages14
JournalChem
Volume1
Issue number2
DOIs
StatePublished - Aug 11 2016

Funding

D.L.W., D.A.H., and B.A.B. are supported by grants R01AI018306 and R01GM117552 from the NIH (NIAID). We thank Professor Richard A. Cerione, Professor Ja-an Annie Ho, Dr. Marc A. Antonyak, and John L. Grazul for helpful discussions and help with cell cultures. Fluorescence imaging data were acquired in the Cornell BRC-Imaging Facility with the shared, NIH-funded (S10RR025502) Zeiss LSM 710 confocal microscope and the NSF-funded (1428922) Zeiss Elyra super resolution microscope (structured illumination microscopy imaging). Y.H., D.A.M., and the electron microscopy and spectroscopy are supported by the Cornell Center for Materials Research funded through the NSF MRSEC program (DMR-1120296).

Keywords

  • SDG3: Good health and well-being

ASJC Scopus subject areas

  • General Chemistry
  • Biochemistry
  • Environmental Chemistry
  • General Chemical Engineering
  • Biochemistry, medical
  • Materials Chemistry

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