Graphene Oxide Nanosheets Toxicity in Mice Is Dependent on Protein Corona Composition and Host Immunity.

Abstract

Two-dimension graphene oxide (GO) nanosheets with high and low serum protein binding profiles (high/low hard-bound protein corona/HC_high/low) are used in this study as model materials and screening tools to investigate the underlying roles of the protein corona on nanomaterial toxicities <i>in vivo</i>. We proposed that the <i>in vivo</i> biocompatibility/nanotoxicity of GO is protein corona-dependent and host immunity-dependent. The hypothesis was tested by injecting HC_high/low GO nanosheets in immunocompetent ICR/CD1 and immunodeficient NOD-<i>scid II2rγ</i>^<i>null</i> mice and performed histopathological and hematological evaluation studies on days 1 and 14 post-injection. HC_low GO induced more severe acute lung injury compared to HC_high GO in both immunocompetent and immunodeficient mice, with the effect being particularly pronounced in immunocompetent animals. Additionally, HC_low GO caused more significant liver injury in both types of mice, with immunodeficient mice being more susceptible to its hepatotoxic effects. Moreover, administration of HC_low GO resulted in increased hematological toxicity and elevated levels of serum pro-inflammatory cytokines in immunocompromised and immunocompetent mice, respectively. Correlation studies were conducted to explore the impact of distinct protein corona compositions on resulting toxicities in both immunocompetent and immunodeficient mice. This facilitated the identification of consistent patterns, aligning with those observed <i>in vitro</i>, thus indicating a robust <i>in vitro-in vivo</i> correlation. This research will advance our comprehension of how hard corona proteins interact with immune cells, leading to toxicity, and will facilitate the development of improved immune-modulating nanomaterials for therapeutic purposes.