Nanoparticle Transport in Proximal Tubules with Rhabdomyolysis‐Induced Necrosis

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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Publication Details

Journal
Angewandte Chemie International Edition
Published
2024-10-18
DOI
https://doi.org/10.1002/anie.202417024
Citations
7
Primary Topic
Muscle and Compartmental Disorders
Type
article
Field-Weighted Citation Impact
4.01

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article

Nanoparticle Transport in Proximal Tubules with Rhabdomyolysis‐Induced Necrosis

Jie Zheng, Yingyu Huang, Mengxiao Yu
7 citations
Angewandte Chemie International Edition
Muscle and Compartmental Disorders
4.01
article

Nanoparticle Transport in Proximal Tubules with Rhabdomyolysis‐Induced Necrosis

Jie Zheng, Yingyu Huang, Mengxiao Yu
article en
7 citations

Abstract

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.

Angewandte Chemie International EditionVol. 64(5)
The University of Texas at Dallas (US)
National Institute of Diabetes and Digestive and Kidney Diseases
Good health and well-being
Openalex Percentile: Top 6%
Muscle and Compartmental Disorders
4.01
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Nanoparticle Transport in Proximal Tubules with Rhabdomyolysis‐Induced Necrosis — Jie Zheng, Yingyu Huang, et al. · Angewandte Chemie International Edition (2024) | TGRS Research Map | TGRS