Nowakowski Adam, Walczak Piotr, Janowski Miroslaw, Lukomska Barbara
1 NeuroRepair Department, Mossakowski Medical Research Centre, Polish Academy of Sciences , Warsaw, Poland .
2 Division of Magnetic Resonance Research, Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine , Baltimore, Maryland.
Stem Cells Dev. 2015 Oct 1;24(19):2219-42. doi: 10.1089/scd.2015.0062. Epub 2015 Aug 26.
Mesenchymal stem cells (MSCs), which can be obtained from various organs and easily propagated in vitro, are one of the most extensively used types of stem cells and have been shown to be efficacious in a broad set of diseases. The unique and highly desirable properties of MSCs include high migratory capacities toward injured areas, immunomodulatory features, and the natural ability to differentiate into connective tissue phenotypes. These phenotypes include bone and cartilage, and these properties predispose MSCs to be therapeutically useful. In addition, MSCs elicit their therapeutic effects by paracrine actions, in which the metabolism of target tissues is modulated. Genetic engineering methods can greatly amplify these properties and broaden the therapeutic capabilities of MSCs, including transdifferentiation toward diverse cell lineages. However, cell engineering can also affect safety and increase the cost of therapy based on MSCs; thus, the advantages and disadvantages of these procedures should be discussed. In this review, the latest applications of genetic engineering methods for MSCs with regenerative medicine purposes are presented.
间充质干细胞(MSCs)可从多种器官获取且易于在体外增殖,是应用最为广泛的干细胞类型之一,已被证明对多种疾病有效。MSCs独特且极为理想的特性包括对损伤区域的高迁移能力、免疫调节特性以及分化为结缔组织表型的天然能力。这些表型包括骨和软骨,这些特性使MSCs具有治疗用途。此外,MSCs通过旁分泌作用发挥其治疗效果,在此过程中靶组织的代谢受到调节。基因工程方法可极大地增强这些特性并拓宽MSCs的治疗能力,包括向多种细胞谱系的转分化。然而,细胞工程也可能影响安全性并增加基于MSCs的治疗成本;因此,应讨论这些操作的优缺点。在本综述中,介绍了基因工程方法在用于再生医学目的的MSCs方面的最新应用。