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化学修饰的碳水化合物缀合物实现高效且选择性的肾脏靶向

Efficient and selective kidney targeting by chemically modified carbohydrate conjugates.

作者信息

Kumar Vikas, Wahane Aniket, Tham Ming Shen, Somlo Stefan, Gupta Anisha, Bahal Raman

机构信息

Department of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269, USA.

Department of Internal Medicine, Yale School of Medicine, New Haven, CT 06520, USA.

出版信息

Mol Ther. 2024 Dec 4;32(12):4383-4400. doi: 10.1016/j.ymthe.2024.10.020. Epub 2024 Nov 12.

Abstract

We investigated a renal tubule-targeting carbohydrate (RENTAC) that can selectively deliver small-molecule and nucleic acid analogs to the proximal convoluted tubules of the kidney following systemic delivery in mice. We comprehensively evaluated anti-miR-21-peptide nucleic acid-RENTAC, and fluorophore-RENTAC conjugates in cell culture and in vivo. We established that RENTAC conjugates showed megalin- and cubilin-dependent endocytic uptake in the immortalized kidney cell line. In vivo biodistribution studies confirmed the retention of RENTAC conjugates in the kidneys for several days compared with other organs. Immunofluorescence staining confirmed the selective distribution of the RENTAC conjugates in proximal convoluted tubules. We further demonstrated proximal convoluted tubule targeting features of RENTAC conjugates in a folic acid-induced kidney fibrosis mouse model. As a biological readout, we targeted miR-33 using antisense peptide nucleic acid (PNA) 33-RENTAC conjugates in the fibrotic kidney disease model. The targeted delivery of PNA 33-RENTAC resulted in slower fibrosis progression and decreased collagen deposition. We also confirmed that the RENTAC ligand did not exert any adverse reactions. Thus, we established that the RENTAC ligand can be used for broad clinical applications targeting the kidneys selectively.

摘要

我们研究了一种肾小管靶向性碳水化合物(RENTAC),在对小鼠进行全身给药后,它能够将小分子和核酸类似物选择性地递送至肾脏的近端曲管。我们在细胞培养和体内实验中全面评估了抗miR-21-肽核酸-RENTAC以及荧光团-RENTAC偶联物。我们证实,RENTAC偶联物在永生化肾细胞系中呈现出依赖巨蛋白和 Cubilin 的内吞摄取。体内生物分布研究证实,与其他器官相比,RENTAC 偶联物在肾脏中可保留数天。免疫荧光染色证实了 RENTAC 偶联物在近端曲管中的选择性分布。我们进一步在叶酸诱导的肾纤维化小鼠模型中证明了 RENTAC 偶联物的近端曲管靶向特性。作为生物学读数,我们在纤维化肾病模型中使用反义肽核酸(PNA)33-RENTAC 偶联物靶向 miR-33。PNA 33-RENTAC 的靶向递送导致纤维化进展减缓且胶原沉积减少。我们还证实 RENTAC 配体未产生任何不良反应。因此,我们确定 RENTAC 配体可用于选择性靶向肾脏的广泛临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1438/11638880/745c3b85298a/fx1.jpg

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