Kheirandish Maryam, Gavgani Somaie Piri, Samiee Shahram
Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
Transfus Apher Sci. 2017 Jun;56(3):392-399. doi: 10.1016/j.transci.2017.03.015. Epub 2017 Mar 31.
In recent years, human umbilical cord blood-derived mesenchymal stem cell (hUB-MSCs) has been regarded as an alternative source for stem cell therapy. In this study, we evaluated the effect of hypoxia preconditioning (HPC) on the expression of Nt-3, GFAP, Nestin, Oct-4 and Nanog genes and proliferative capacity of hUB-MSCs in comparison with normoxic conditions. HPC+Hypoxia protocol includes cultured hUB-MSCs for 15min at 2.5% O and after that reoxygenation for 30min at 21% O (HPC), and then hypoxia preconditioned hUB-MSCs subjected to 2.5% O for 72h (Hypoxia). Conclusively, the results showed that hypoxic preconditioning is an effective strategy for enhancing proliferation capacity of hUB-MSCs, and also can trigger expression of some of the neural genes. In addition, the concept of involvement of oxygen tension in the expression of some of the neural genes of hUB-MSCs would be a good sign of enhanced neural differentiation potential in vitro.
近年来,人脐带血间充质干细胞(hUB-MSCs)被视为干细胞治疗的替代来源。在本研究中,我们评估了低氧预处理(HPC)与常氧条件相比,对hUB-MSCs中Nt-3、GFAP、巢蛋白、Oct-4和Nanog基因表达以及增殖能力的影响。HPC+低氧方案包括将hUB-MSCs在2.5%氧气浓度下培养15分钟,然后在21%氧气浓度下复氧30分钟(HPC),接着将经过低氧预处理的hUB-MSCs在2.5%氧气浓度下培养72小时(低氧)。最终,结果表明低氧预处理是增强hUB-MSCs增殖能力的有效策略,并且还能触发一些神经基因的表达。此外,氧张力参与hUB-MSCs某些神经基因表达的概念将是其体外神经分化潜能增强的良好迹象。