Huang Shiyi, Li Sijie, Liu Yanlei, Ghalandari Behafarid, Hao Ling, Huang Chengjie, Su Wenqiong, Ke Yuqing, Cui Daxiang, Zhi Xiao, Ding Xianting
State Key laboratory of Oncogenes and Related Genes, Institute for Personalized Medicine, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, 200030, China.
Shanghai Engineering Center for Intelligent Diagnosis and Treatment Instrument, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
Adv Healthc Mater. 2022 Apr;11(8):e2102439. doi: 10.1002/adhm.202102439. Epub 2021 Dec 10.
The boosting exploitation of graphene oxide (GO) increases exposure risk to human beings. However, as primary defender in the first immune line, neutrophils' mechanism of defensive behavior toward GO remains unclear. Herein, we discovered that neutrophils recognize and defensively degrade GO in a lateral dimension dependent manner. The micrometer-sized GO (mGO) induces NETosis by releasing neutrophil extracellular traps (NETs), while nanometer-sized GO (nGO) elicits neutrophil degranulation. The two neutrophils' defensive behaviors are accompanied with generation of reactive oxygen species and activation of p-ERK and p-Akt kinases. However, mGO-induced NETosis is NADPH oxidase (NOX)-independent while nGO-triggered degranulation is NOX-dependent. Furthermore, myeloperoxidase (MPO) is determinant mediator despite distinct neutrophil phenotypes. Neutrophils release NETs comprising of MPO upon activated with mGO, while MPO is secreted via nGO-induced degranulation. Moreover, the binding energy between MPO and GO is calculated to be 69.8728 kJ mol , indicating that electrostatic interactions mainly cause the spontaneous binding process. Meanwhile, the central enzymatic biodegradation occurs at oxygenic active sites and defects on GO. Mass spectrometry analysis deciphers the degradation products are biocompatible molecules like flavonoids and polyphenols. This study provides fundamental evidence and practical guidance for nanotechnology based on GO, including vaccine adjuvant, implantable devices, and energy storage.
氧化石墨烯(GO)的广泛应用增加了人类的接触风险。然而,作为第一道免疫防线的主要防御者,中性粒细胞对GO的防御行为机制尚不清楚。在此,我们发现中性粒细胞以横向维度依赖的方式识别并防御性降解GO。微米级GO(mGO)通过释放中性粒细胞胞外陷阱(NETs)诱导NETosis,而纳米级GO(nGO)引发中性粒细胞脱颗粒。这两种中性粒细胞的防御行为都伴随着活性氧的产生以及p-ERK和p-Akt激酶的激活。然而,mGO诱导的NETosis不依赖于烟酰胺腺嘌呤二核苷酸磷酸氧化酶(NOX),而nGO触发的脱颗粒依赖于NOX。此外,尽管中性粒细胞表型不同,髓过氧化物酶(MPO)是决定性介质。mGO激活后,中性粒细胞释放由MPO组成的NETs,而MPO通过nGO诱导的脱颗粒分泌。此外,计算得出MPO与GO之间的结合能为69.8728 kJ/mol,表明静电相互作用是导致自发结合过程的主要原因。同时,核心酶促生物降解发生在GO的含氧活性位点和缺陷处。质谱分析表明降解产物是生物相容性分子,如黄酮类化合物和多酚。本研究为基于GO的纳米技术提供了基础证据和实践指导,包括疫苗佐剂、可植入装置和能量存储。