Size and ligand effects of gold nanoclusters in alteration of organellar state and translocation of transcription factors in human primary astrocytes. Issue 5 (2nd February 2021)

• Record Type: Journal Article
• Authors: Gran, Evan Rizzel; Bertorelle, Franck; Fakhouri, Hussein; Antoine, Rodolphe; Perić Bakulić, Martina; Sanader Maršić, Željka; Bonačić-Koutecký, Vlasta; Blain, Manon; Antel, Jack; Maysinger, Dusica
• Is Part Of: Nanoscale. Volume 13:Issue 5(2021)
• Page Start: 3173
• Page End: 3183
• Publication Date: 2021-02-02
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/d0nr06401g
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Ultra-small gold nanoclusters are atomically precise structures that modulate organelles and redox-responsive transcription factors in human primary astrocytes. Abstract : Ultra-small gold nanoclusters (AuNCs) with designed sizes and ligands are gaining popularity for biomedical purposes and ultimately for human imaging and therapeutic applications. Human non-tumor brain cells, astrocytes, are of particular interest because they are abundant and play a role in functional regulation of neurons under physiological and pathological conditions. Human primary astrocytes were treated with AuNCs of varying sizes (Au10, Au15, Au18, Au25 ) and ligand composition (glutathione, polyethylene glycol, N -acetyl cysteine). Concentration and time-dependent studies showed no significant cell loss with AuNC concentrations <10 μM. AuNC treatment caused marked differential astrocytic responses at the organellar and transcription factor level. The effects were exacerbated under severe oxidative stress induced by menadione. Size-dependent effects were most remarkable with the smallest and largest AuNCs (10, 15 Au atoms versus 25 Au atoms) and might be related to the accessibility of biological targets toward the AuNC core, as demonstrated by QM/MM simulations. In summary, these findings suggest that AuNCs are not inert in primary human astrocytes, and that their sizes play a critical role in modulation of organellar and redox-responsive transcription factor homeostasis.