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多聚甘油胺包覆纳米片靶向细胞游离 DNA 以减轻急性肾损伤。

Polyglycerol-Amine Covered Nanosheets Target Cell-Free DNA to Attenuate Acute Kidney Injury.

机构信息

Department of Nephrology, The First Affiliated Hospital, Sun Yat-sen University, NHC Key Laboratory of Clinical Nephrology, Guangdong Provincial Key Laboratory of Nephrology, Guangzhou, Guangdong, 510080, China.

Department of Otolaryngology, the Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, Guangdong, 510655, China.

出版信息

Adv Sci (Weinh). 2023 Aug;10(23):e2300604. doi: 10.1002/advs.202300604. Epub 2023 Jun 5.

Abstract

Increased levels of circulating cell-free DNA (cfDNA) are associated with poor clinical outcomes in patients with acute kidney injury (AKI). Scavenging cfDNA by nanomaterials is regarded as a promising remedy for cfDNA-associated diseases, but a nanomaterial-based cfDNA scavenging strategy has not yet been reported for AKI treatment. Herein, polyglycerol-amine (PGA)-covered MoS nanosheets with suitable size are synthesized to bind negatively charged cfDNA in vitro, in vivo and ex vivo models. The nanosheets exhibit higher cfDNA binding capacity than polymer PGA and PGA-based nanospheres owing to the flexibility and crimpability of their 2D backbone. Moreover, with low cytotoxicity and mild protein adsorption, the nanosheets effectively reduced serum cfDNA levels and predominantly accumulated in the kidneys to inhibit the formation of neutrophil extracellular traps and renal inflammation, thereby alleviating both lipopolysaccharide and ischemia-reperfusion induced AKI in mice. Further, they decreased the serum cfDNA levels in samples from AKI patients. Thus, PGA-covered MoS nanosheets can serve as a potent cfDNA scavenger for treating AKI and other cfDNA-associated diseases. In addition, this work demonstrates the pivotal feature of a 2D sheet-like structure in the development of the cfDNA scavenger, which can provide a new insight into the future design of nanoplatforms for modulating inflammation.

摘要

循环无细胞 DNA(cfDNA)水平升高与急性肾损伤(AKI)患者的临床预后不良有关。纳米材料清除 cfDNA 被认为是治疗 cfDNA 相关疾病的一种有前途的方法,但尚未有基于纳米材料的 cfDNA 清除策略被报道用于 AKI 的治疗。在此,合成了具有合适尺寸的覆盖有聚甘油-胺(PGA)的 MoS 纳米片,以在体外、体内和离体模型中结合带负电荷的 cfDNA。由于其 2D 主链的柔韧性和卷曲性,纳米片表现出比聚合物 PGA 和基于 PGA 的纳米球更高的 cfDNA 结合能力。此外,由于其低细胞毒性和温和的蛋白质吸附性,纳米片有效地降低了血清 cfDNA 水平,并主要在肾脏中积累,以抑制中性粒细胞胞外诱捕网和肾脏炎症的形成,从而缓解脂多糖和缺血再灌注诱导的 AKI 小鼠。此外,它们降低了 AKI 患者样本中的血清 cfDNA 水平。因此,PGA 覆盖的 MoS 纳米片可用作治疗 AKI 和其他 cfDNA 相关疾病的有效 cfDNA 清除剂。此外,这项工作证明了 2D 片状结构在开发 cfDNA 清除剂中的关键特征,这为未来设计用于调节炎症的纳米平台提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7e6/10427348/3eccfe32da81/ADVS-10-2300604-g004.jpg

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