精准医学:免疫惰性外泌体的设计用于靶向基因传递。

IF 3.3 4区 医学 Q2 GENETICS & HEREDITY
Fawzy A Saad
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引用次数: 0

摘要

外泌体是细胞外囊泡中最小的,细胞外囊泡还包括凋亡小体和微囊泡。外泌体是天然的纳米载体,在细胞内通讯中起关键作用,由疏水脂质双层膜和亲水核组成。外泌体的膜组成与产生外泌体的亲本细胞相似。正常情况下,外泌体膜含有二酰基甘油、神经酰胺、胆固醇和各种表面蛋白,包括四跨蛋白和Lamb2。几乎所有类型的细胞都通过胞吐作用将外泌体分泌到体液中,包括干细胞、上皮细胞、内皮细胞、免疫细胞、肿瘤细胞、神经元、肥大细胞、少突胶质细胞、网状细胞、巨噬细胞、血小板和星形胶质细胞。每种细胞类型都表达一种携带各种生物活性分子的独特类型的外泌体。外泌体是生物活性货物的主要转运体,包括酶、受体、生长和转录因子、核酸、脂质和其他代谢物,它们强烈影响受体细胞的生理。外泌体不仅是有效的药物和基因递送纳米载体,而且在疾病诊断、组织再生和免疫调节方面具有潜在的作用。外泌体存在于各种体液中,包括血浆、血清、唾液、乳汁、鼻分泌物、尿液、羊水、精液和脑脊液等。干细胞制造的外泌体是潜在的天然疗法,这是由于它们具有恢复活力的货物和跨越生物屏障的能力。然而,天然外泌体在血液中的低效率货物转移和短寿命阻碍了它们在治疗干预中的进展。亲本细胞的基因工程允许将特定的治疗货物装载到新生成的外泌体的腔内和/或在其表面显示某些归巢肽或配体,从而延长其寿命并精确地运送到特定的器官或组织。这篇综述探讨了通过亲本细胞工程创造的设计外泌体,以及它们在指导将定制的治疗货物递送到特定器官同时避开宿主的先天免疫反应的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Precision Medicine: Design of Immune Inert Exosomes for Targeted Gene Delivery.

Exosomes represent the smallest size among extracellular vesicles, which also include apoptotic bodies and microvesicles. Exosomes are natural nanocarriers that play a key role in intracellular communication, consisting of a hydrophobic lipid bilayer membrane and a hydrophilic core. The membrane compositions of exosomes are similar to those of the parent cells from which they are generated. Normally, the exosome membrane contains diacylglycerol, ceramide, cholesterol, and various surface proteins, including tetraspanins and Lamb2. Almost all cell types secrete exosomes into body fluids through exocytosis, including stem cells, epithelial cells, endothelial cells, immune cells, tumor cells, neurons, mast cells, oligodendrocytes, reticulocytes, macrophages, platelets, and astrocytes. Every cell type expresses a distinct type of exosomes carrying various bioactive molecules. Exosomes are major transporters of bioactive cargo, including enzymes, receptors, growth and transcription factors, nucleic acids, lipids, and other metabolites, which strongly affect the physiology of recipient cells. Exosomes are not only potent drug and gene delivery nanocarriers, but also have potential for disease diagnosis, tissue regeneration, and immunomodulation. Exosomes are present in various body fluids, including plasma, serum, saliva, milk, nasal secretions, urine, amniotic fluid, semen, and cerebrospinal fluid, among others. Stem cell-made exosomes are potential natural therapeutics, which is due to their rejuvenating cargo and ability to cross biological barriers. However, natural exosomes' inefficient cargo transfer and short lifespan in the bloodstream have hindered their progress in therapeutic interventions. Genetic engineering of the parent cell allows for loading specific therapeutic cargo into the lumen of newly generated exosomes and/or displaying certain homing peptides or ligands at their surface, leading to extension of their lifespan and precise delivery to specific organs or tissues. This minireview explores the creation of designer exosomes through parent cell engineering and their utilization for guiding the delivery of tailored therapeutic cargo to specific organs while evading the host's innate immune response.

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来源期刊
Current gene therapy
Current gene therapy 医学-遗传学
CiteScore
6.70
自引率
2.80%
发文量
46
期刊介绍: Current Gene Therapy is a bi-monthly peer-reviewed journal aimed at academic and industrial scientists with an interest in major topics concerning basic research and clinical applications of gene and cell therapy of diseases. Cell therapy manuscripts can also include application in diseases when cells have been genetically modified. Current Gene Therapy publishes full-length/mini reviews and original research on the latest developments in gene transfer and gene expression analysis, vector development, cellular genetic engineering, animal models and human clinical applications of gene and cell therapy for the treatment of diseases. Current Gene Therapy publishes reviews and original research containing experimental data on gene and cell therapy. The journal also includes manuscripts on technological advances, ethical and regulatory considerations of gene and cell therapy. Reviews should provide the reader with a comprehensive assessment of any area of experimental biology applied to molecular medicine that is not only of significance within a particular field of gene therapy and cell therapy but also of interest to investigators in other fields. Authors are encouraged to provide their own assessment and vision for future advances. Reviews are also welcome on late breaking discoveries on which substantial literature has not yet been amassed. Such reviews provide a forum for sharply focused topics of recent experimental investigations in gene therapy primarily to make these results accessible to both clinical and basic researchers. Manuscripts containing experimental data should be original data, not previously published.
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