人类干细胞的比较特征

O. Pototskaya, K. Shevchenko
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引用次数: 0

摘要

干细胞治疗是临床医学最有前途的治疗方法之一;含SC的产品正在临床试验中进行积极研究,其中一些产品已经在全球许多国家正式批准用于治疗。因此,现代医学的快速发展方向应在医科大学的教育计划中得到适当的反映,使人们对SC亚型及其性质和潜在风险有基本的了解。本综述的目的是对供应链的类型、采购方法和雇佣前景进行比较分析。SCs可根据供体年龄进行分组。胚胎干细胞是从囊胚中分离出来的,通过体外受精、克隆、半克隆或孤雌生殖获得(雄激素发育和雌性发育的SCs)。胎儿SCs可以从出生前的胚胎和胎儿组织或从流产和流产材料(包括异位妊娠)中分离出来。胎儿中有一类特殊的围产期胚外干细胞,它们是在出生后从胚外器官(脐带、羊膜、胎盘)中获得的;其中有造血细胞、间充质细胞、上皮细胞和蜕细胞。成体(体细胞的,组织特异性的)SCs可以在整个生命过程中从成体的不同组织和器官中分离;它们的性质取决于它们的所在地和捐赠者的年龄。此外,可以通过修饰基因表达从成熟细胞人工制备SCs;它们在诱导多能干细胞组中结合在一起。每一类SCs都不是同质的,有其各自的优缺点。此外,应用由干细胞产生的外泌体作为细胞治疗的替代方案也被考虑。
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Comparative characteristics of human stem cells
Stem cell (SC) therapy is one of the most perspective methods of clinical medicine; SC containing products are actively investigated in clinical trials, while some of them are already officially approved for treatment in many countries worldwide. So quickly developing direction of modern medicine should be properly reflected in educational programs of medical universities, providing basic understanding of SC subtypes, their properties and potential risks. The purpose of this review is to perform comparative analysis of SC types, methods of their procurement and perspectives of their employment. SCs could be divided into groups according to the age of the donor organism. Embryonic SCs are isolated from blastocyst, obtained as a result of extracorporeal fertilization, cloning, semicloning or parthenogenesis (androgenetic and gynogenetic SCs). Fetal SCs could be isolated from embryonic and fetal tissues before the birth or from miscarriages and abortion material (including ectopic pregnancy). Among fetal there is and especial group of perinatal extraembryonic SCs which are obtained from extraembryonic organs (umbilical cord, amnion, placenta) after the birth; among them hematopoietic, mesenchymal, epithelial and decidual cells are distinguished. Adult (somatic, tissue specific) SCs could be isolated from different tissues and organs of adult organism throughout the life; their properties depend on the place of their localization and age of the donor. Additionally, SCs could be created artificially from mature cells by modification of gene expression; they are united in the group of induced pluripotent SCs. Every group of SCs is not homogenous and has its advances and drawbacks, analyzed in this review. Also, application of exosomes produced by stem cells as an alternative of cellular therapy is considered.
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