Department of Molecular Biology and Genetic Engineering, Stem Cell Technology Research Center, Tehran, Iran.
Appl Biochem Biotechnol. 2014 Feb;172(4):2055-69. doi: 10.1007/s12010-013-0633-0. Epub 2013 Dec 11.
Micro RNAs (miRNAs) are a novel class of non-coding regulatory RNA molecules that contribute to post-transcriptional gene regulation. Recent studies have demonstrated that specific miRNAs such as miR-150, miR-154, and miR-451 have key roles in erythropoiesis. To date, stimulatory cytokines are considered as unique effectors for in vitro differentiation of HSCs to erythropoietic lineage. However, the use of these factors is not cost-effective for clinical applications and therapeutic strategies. Here, we present a novel and cost-effective strategy in which miRNAs expression modulation promotes erythroid differentiation in HSCs in the absence of any extrinsic factors. Thus, CD133(+) hematopoietic stem cells purified from human umbilical cord blood were treated with pre-miR-451 containing lentiviruses, anti-miR-150 and anti-miR-154 in the absence of growth factors and cytokines. Obtained results indicated that miR-451 upregulation and miR-150 downregulation have positive effect on GATA-1, FOG-1, and EKLF, CD71 and CD235a genes expression and induce hemoglobinization efficiently. However, downregulation of miR-154 had no effect on erythropoiesis indexes compared to that observed in the control group. In conclusion, the data presented here for the first time demonstrate that expression modulation of miR-451 and miR-150 could be an efficient alternative to stimulatory cytokines for CD133(+) differentiation into erythroid lineage. Modulation of erythropoiesis in stem cells via miRNA holds promising potential for vascular tissue engineering and regenerative medicine applications.
微小 RNA(miRNAs)是一类新型的非编码调控 RNA 分子,参与转录后基因调控。最近的研究表明,特定的 miRNAs,如 miR-150、miR-154 和 miR-451,在红细胞生成中具有关键作用。迄今为止,刺激细胞因子被认为是体外诱导 HSCs 向红细胞谱系分化的唯一效应因子。然而,这些因素的使用在临床应用和治疗策略方面并不具有成本效益。在这里,我们提出了一种新的、具有成本效益的策略,即通过调节 miRNAs 的表达来促进 HSCs 中的红细胞分化,而无需任何外在因素。因此,我们从人脐血中纯化 CD133(+)造血干细胞,在没有生长因子和细胞因子的情况下,用含有 pre-miR-451 的慢病毒、抗 miR-150 和抗 miR-154 处理。结果表明,miR-451 的上调和 miR-150 的下调对 GATA-1、FOG-1 和 EKLF、CD71 和 CD235a 基因的表达有积极影响,并能有效地诱导血红蛋白化。然而,与对照组相比,miR-154 的下调对红细胞生成指标没有影响。总之,本文首次表明,miR-451 和 miR-150 的表达调控可以替代刺激细胞因子,有效地将 CD133(+)分化为红细胞谱系。通过 miRNA 调节干细胞中的红细胞生成在血管组织工程和再生医学应用中具有很大的潜力。