Nanoparticle Transport in Proximal Tubules with Rhabdomyolysis‐Induced Necrosis

细胞内 坏死 急性肾损伤 细胞外 间隙 横纹肌溶解症 急性肾小管坏死 管腔(解剖学) 胶体金 细胞凋亡 化学 病理 纳米颗粒 细胞生物学 生物物理学 医学 生物 纳米技术 材料科学 生物化学 内科学 泌尿科
作者
Yingyu Huang,Jie Zheng,Mengxiao Yu
出处
期刊:Angewandte Chemie [Wiley]
卷期号:64 (5): e202417024-e202417024 被引量:7
标识
DOI:10.1002/anie.202417024
摘要

Renal-clearable engineered nanoparticles are being explored for their potential to deliver therapeutic agents for kidney disease treatment. A fundamental understanding of how these nanoparticles accumulate in diseased kidneys at the cellular level is essential to enhance their effectiveness and minimize side effects on adjacent healthy tissues. Herein, we report that the accumulation of glutathione-coated, near-infrared emitting gold nanoparticles (GS-AuNPs) correlates strongly with the necrotic stages of injured proximal tubular cells. Using a rhabdomyolysis-induced acute kidney injury (AKI) mouse model, we observed that GS-AuNPs were significantly accumulated in the extracellular lumen of proximal tubular epithelial cells (PTECs) at advanced necrotic stage, where cellular debris and released intracellular contents impeded their clearance. In contrast, during early necrosis, GS-AuNPs were still cleared through the unobstructed lumen. Additionally, intracellular uptake of GS-AuNPs was significantly reduced across all necrotic stages. These findings underscore the need for new strategies to design nanoparticles that can effectively target and be taken up by the diseased tubular cells before extensive necrosis occurs; so that nanoparticle-mediated drug delivery for kidney disease treatment can be achieved with desired efficacy and precision.
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