结合分化细胞外囊泡和中间中胚层细胞的生物活性支架的肾组织再生。

IF 8.1 Q1 ENGINEERING, BIOMEDICAL Biomaterials research Pub Date : 2023-12-05 DOI:10.1186/s40824-023-00471-x
Seung-Gyu Cha, Won-Kyu Rhim, Jun Yong Kim, Eun Hye Lee, Seung Yeon Lee, Jeong Min Park, Jeoung Eun Lee, Hyeji Yoon, Chun Gwon Park, Bum Soo Kim, Tae Gyun Kwon, Youngmi Lee, Dong Ryul Lee, Dong Keun Han
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引用次数: 0

摘要

背景:为了克服目前慢性肾脏疾病(CKD)替代疗法的局限性,组织工程介导的再生策略已经证明了完全肾脏组织再生的可能性。考虑到与肾基底细胞再生相关的挑战,结合中胚层(IM)细胞和生物活性材料来控制支撑支架细胞的生物活性应该被认为是一种可行的方法,可以通过肾脏分化来实现复杂肾脏结构的再生。方法:将蓖麻油酸接枝的Mg(OH)2 (M)、细胞外基质(E)和α硫辛酸偶联的ZnO (Z)等关键生物活性成分整合到可生物降解的多孔PLGA (P)平台中,制备PMEZ支架。此外,我们利用中间中胚层分化过程中分离的分化细胞外囊泡(differentiation extracellular vesicles, dEV)分化为肾祖细胞,并在3/4肾切除小鼠模型中,连续加入IM细胞,使其分化为肾祖细胞,促进肾组织再生。结果:利用细胞外囊泡分化使IM在不需要其他分化因子的情况下向肾祖细胞分化。这导致了各种再生相关生物活性的改善,包括小管和足细胞再生、抗纤维化、血管生成和抗炎症。最后,在小鼠损伤模型中植入PMEZ/dEV/IM支架,使肾脏功能得到恢复。结论:我们的研究表明,利用可生物降解的基于plga的支架,包括能够分化成各种肾祖细胞的多能细胞以及支持成分,可以促进通过3/4肾切除术模拟CKD的小鼠模型的肾组织再生。
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Kidney tissue regeneration using bioactive scaffolds incorporated with differentiating extracellular vesicles and intermediate mesoderm cells.

Background: To overcome the limitations of current alternative therapies for chronic kidney disease (CKD), tissue engineering-mediated regeneration strategies have demonstrated the possibilities for complete kidney tissue regeneration. Given the challenges associated with the reproducibility of renal basal cells, the incorporation of intermediate mesoderm (IM) cells and bioactive materials to control bioactivities of cells with supported scaffolds should be considered as a viable approach to enable the regeneration of the complex kidney structure via renal differentiation.

Methods: We developed PMEZ scaffolds by combining crucial bioactive components, such as ricinoleic acid-grafted Mg(OH)2 (M), extracellular matrix (E), and alpha lipoic acid-conjugated ZnO (Z) integrated into biodegradable porous PLGA (P) platform. Additionally, we utilized differentiating extracellular vesicles (dEV) isolated during intermediate mesoderm differentiation into kidney progenitor cells, and IM cells were serially incorporated to facilitate kidney tissue regeneration through their differentiation into kidney progenitor cells in the 3/4 nephrectomy mouse model.

Results: The use of differentiating extracellular vesicles facilitated IM differentiation into kidney progenitor cells without additional differentiation factors. This led to improvements in various regeneration-related bioactivities including tubule and podocyte regeneration, anti-fibrosis, angiogenesis, and anti-inflammation. Finally, implanting PMEZ/dEV/IM scaffolds in mouse injury model resulted in the restoration of kidney function.

Conclusions: Our study has demonstrated that utilizing biodegradable PLGA-based scaffolds, which include multipotent cells capable of differentiating into various kidney progenitor cells along with supporting components, can facilitate kidney tissue regeneration in the mouse model that simulates CKD through 3/4 nephrectomy.

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