Exosome-mediated renal protection: Halting the progression of fibrosis

微泡 纤维化 再生(生物学) 外体 炎症 肾脏疾病 医学 癌症研究 细胞外基质 胞外囊泡 急性肾损伤 免疫学 生物 细胞生物学 病理 内科学 小RNA 生物化学 基因
作者
Chuanqi Liu,Qingfeng Li,Jian‐xing Ma,Baisong Lu,Tracy Criswell,Yuanyuan Zhang
出处
期刊:Genes and Diseases [Elsevier BV]
卷期号:11 (6): 101117-101117
标识
DOI:10.1016/j.gendis.2023.101117
摘要

Renal fibrosis is a complex and multifactorial process that involves inflammation, cell proliferation, collagen, and fibronectin deposition in the kidney, ultimately leading to chronic kidney disease and even end-stage renal disease. The main goal of treatment is to slow down or halt the progression of fibrosis and to improve or preserve kidney function. Despite significant progress made in understanding the mechanisms underlying renal fibrosis, current therapies have limited renal protection as the disease progresses. Exosomes derived from stem cells are a newer area of research for the treatment of renal fibrosis. Exosomes as nano-sized extracellular vesicles carry proteins, lipids, and nucleic acids, which can be taken up by local or distant cells, serving as mediators of intercellular communication and as drug delivery vehicles. Exosomes deliver molecules that reduce inflammation, renal fibrosis, and extracellular matrix protein production, and promote tissue regeneration in animal models of kidney disease. Additionally, they have several advantages over stem cells, such as being non-immunogenic, having a low risk of tumor formation, and being easier to produce and store. This review describes the use of natural and engineered exosomes containing therapeutic agents capable of mediating anti-inflammatory and anti-fibrotic processes during both acute kidney injury and chronic kidney disease. Exosome-based therapies will be compared with stem cell-based treatments for tissue regeneration, with a focus on renal protection. Finally, future directions and strategies for improving the therapeutic efficacy of exosomes are discussed.

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