Multifunctional extracellular vesicles and edaravone-loaded scaffolds for kidney tissue regeneration by activating GDNF/RET pathway

IF 13.4 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY Nano Convergence Pub Date : 2024-10-26 DOI:10.1186/s40580-024-00450-5
Seung Yeon Lee, Jeong Min Park, Won-Kyu Rhim, Eun Hye Lee, Sang-Hyuk Lee, Jun Yong Kim, Seung-Gyu Cha, Sun Hong Lee, Boram Kim, Dong-Youn Hwang, Seungsoo Rho, Tae-Keun Ahn, Bum Soo Kim, Dong Keun Han
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Abstract

With the severity of chronic kidney disease worldwide, strategies to recover renal function via tissue regeneration provide alternatives to kidney replacement therapy. To exclude side effects from direct cell transplantation, extracellular vesicles (EVs) are great substitutes representing paracrine cell signaling. To build three-dimensional structures for implantation into the 5/6 nephrectomy model by incorporating bioactive materials, including multifunctional EVs (mEVs), porous PMEZE/mEV scaffolds were developed in combination with edaravone (EDV; E) and mEV based on PMEZ scaffolds with PLGA (P), MH-RA (M), ECM (E), ZnO-ALA (Z). The oxygen free radical scavenger EDV was incorporated to induce tubular regeneration. mEVs were engineered to serve regenerative activities with a combination of two EVs from SDF-1α overexpressed tonsil-derived mesenchymal stem cells (sEVs) and intermediate mesoderm (IM) cells during differentiation into kidney progenitor cells (dEVs). mEVs displayed beneficial effects on regeneration by facilitating migration and inducing differentiation of surrounding stem cells, and EDV improved kidney function by regulating the GDNF/RET pathway and their downstream genes. The promotion of MSC recruitment was confirmed with sEV particles number dependently, and the regulation of the GDNF/RET pathway by the effect of EDV and its enhanced effect by mEVs were elucidated using in vitro analysis. The regeneration of tubules was additionally demonstrated through the increased expression of aquaporin-1 (AQP-1) and cadherin-16 (CDH16) for proximal tubules, and calbindin and PAX2 for distal tubules in the renal defect model. With these, structural regeneration and functional recovery were achieved with kidney regeneration in the 5/6 nephrectomy mice model.

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通过激活 GDNF/RET 通路实现肾组织再生的多功能细胞外囊泡和依达拉奉负载支架
随着全球慢性肾病的严重化,通过组织再生恢复肾功能的策略为肾脏替代疗法提供了替代方案。为了排除直接细胞移植的副作用,细胞外囊泡(EVs)是代表旁分泌细胞信号的最佳替代品。为了结合生物活性材料(包括多功能 EVs(mEVs))构建三维结构植入 5/6 肾切除模型,研究人员开发了结合依达拉奉(EDV;E)的多孔 PMEZE/mEV 支架,以及基于含有 PLGA(P)、MH-RA(M)、ECM(E)、ZnO-ALA(Z)的 PMEZ 支架的 mEV。mEVs 是由 SDF-1α 过度表达的扁桃体间充质干细胞(sEVs)和分化成肾祖细胞(dEVs)过程中的中间中胚层(IM)细胞的两种 EVs 组合而成,具有再生活性。mEVs通过促进周围干细胞的迁移和诱导分化对再生产生了有益的影响,EDV通过调节GDNF/RET通路及其下游基因改善了肾功能。sEV颗粒对间叶干细胞募集的促进作用与数量有关,EDV对GDNF/RET通路的调节作用以及mEV对其增强作用通过体外分析得以阐明。此外,在肾脏缺损模型中,近端肾小管的aquaporin-1(AQP-1)和cadherin-16(CDH16)以及远端肾小管的calbindin和PAX2的表达增加,也证明了肾小管的再生。有了这些,5/6 肾切除小鼠模型的肾脏再生实现了结构再生和功能恢复。
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来源期刊
Nano Convergence
Nano Convergence Engineering-General Engineering
CiteScore
15.90
自引率
2.60%
发文量
50
审稿时长
13 weeks
期刊介绍: Nano Convergence is an internationally recognized, peer-reviewed, and interdisciplinary journal designed to foster effective communication among scientists spanning diverse research areas closely aligned with nanoscience and nanotechnology. Dedicated to encouraging the convergence of technologies across the nano- to microscopic scale, the journal aims to unveil novel scientific domains and cultivate fresh research prospects. Operating on a single-blind peer-review system, Nano Convergence ensures transparency in the review process, with reviewers cognizant of authors' names and affiliations while maintaining anonymity in the feedback provided to authors.
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