Nanoscale detection of carbon dots-induced changes in actin skeleton of neural cells.

[Display omitted] • 1. AFM-based biophysical measurements are performed on a neural cell. • 2. Exposure to high-dose carbon dots affects cellular mechanics and morphology. • 3. Actin filaments are disorganized in the cells after exposure to high-dose carbon dots. • 4. Biological studies validate the cytotoxic effects disclosed by AFM. • 5. AFM is a powerful biophysical tool for the study of cell-nanomaterials interactions. Understanding the cytotoxicity of fluorescent carbon dots (CDs) is crucial for their applications, and various biochemical assays have been used to study the effects of CDs on cells. Knowledge on the effects of CDs from a biophysical perspective is integral to the recognition of their cytotoxicity, however the related information is very limited. Here, we report that atomic force microscopy (AFM) can be used as an effective tool for studying the effects of CDs on cells from the biophysical perspective. We achieve this by integrating AFM-based nanomechanics with AFM-based imaging. We demonstrate the performance of this method by measuring the influence of CDs on living human neuroblastoma (SH-SY5Y) cells at the single-cell level. We find that high-dose CDs can mechanically induce elevated normalized hysteresis (energy dissipation during the cell deformation) and structurally impair actin skeleton. The nanomechanical change highly correlates with the alteration of actin filaments, indicating that CDs-induced changes in SH-SY5Y cells are revealed in-depth from the AFM-based biophysical aspect. We validate the reliability of the biophysical observations using conventional biological methods including cell viability test, fluorescent microscopy, and western blot assay. Our work contributes new and significant information on the cytotoxicity of CDs from the biophysical perspective. [ABSTRACT FROM AUTHOR]