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干细胞衍生的外泌体微小RNA作为血管衰老相关疾病的治疗方法

Stem Cell-derived Exosomal MicroRNA as Therapy for Vascular Age-related Diseases.

作者信息

Ren Hang, Guo Ziyuan, Liu Yang, Song Chunli

机构信息

Department of Cardiovascular Internal Medicine, the Second Hospital of Jilin University, Changchun, China.

出版信息

Aging Dis. 2022 Jun 1;13(3):852-867. doi: 10.14336/AD.2021.1110. eCollection 2022 Jun.

Abstract

Vascular age-related diseases describe a group of age-related chronic diseases that result in a considerable healthcare burden to society. Vascular aging includes structural changes and dysfunctions of endothelial cells (ECs) and smooth muscle cells (SMCs) in blood vessels. Compared with conventional treatment for vascular age-related diseases, stem cell (SC) therapy elicits better anti-aging effects the inhibition/delay ECs and SMCs from entering senescence. Exosomal noncoding RNA (ncRNAs) in vascular aging and stem cell-derived exosomal microRNAs (SCEV-miRNAs), especially in mesenchymal stem cells, have an important role in the development of age-related diseases. This review summarizes SCEV-miRNAs of diverse origins that may play a vital role in treating subclinical and clinical stages of vascular age-related disorders. We further explored possible age-related pathways and molecular targets of SCEV-miRNA, which are associated with dysfunctions of ECs and SMCs in the senescent stage. Moreover, the perspectives and difficulties of SCEV-miRNA clinical translation are discussed. This review aims to provide greater understanding of the biology of vascular aging and to identify critical therapeutic targets for SCEV-miRNAs. Though still in its infancy, the potential value of SCEV-miRNAs for vascular age-related diseases is clear.

摘要

血管衰老相关疾病是指一组与年龄相关的慢性疾病,给社会带来了相当大的医疗负担。血管衰老包括血管内皮细胞(ECs)和平滑肌细胞(SMCs)的结构变化和功能障碍。与血管衰老相关疾病的传统治疗方法相比,干细胞(SC)疗法具有更好的抗衰老效果,能够抑制/延缓ECs和SMCs进入衰老状态。血管衰老中的外泌体非编码RNA(ncRNAs)和干细胞衍生的外泌体微小RNA(SCEV-miRNAs),尤其是间充质干细胞中的此类物质,在衰老相关疾病的发展中具有重要作用。本综述总结了不同来源的SCEV-miRNAs,它们可能在治疗血管衰老相关疾病的亚临床和临床阶段发挥关键作用。我们进一步探讨了SCEV-miRNA可能的与衰老相关的途径和分子靶点,这些靶点与衰老阶段ECs和SMCs的功能障碍有关。此外,还讨论了SCEV-miRNA临床转化的前景和困难。本综述旨在更深入地了解血管衰老的生物学机制,并确定SCEV-miRNAs的关键治疗靶点。尽管仍处于起步阶段,但SCEV-miRNAs对血管衰老相关疾病的潜在价值是显而易见的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6df/9116915/0283784edd0d/AD-13-3-852-g1.jpg

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