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miR-451 的上调,可独立于细胞因子鸡尾酒诱导 CD133+细胞的红系分化。

miR-451 Up-regulation, Induce Erythroid Differentiation of CD133+cells Independent of Cytokine Cocktails.

机构信息

Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Iran J Basic Med Sci. 2013 Jun;16(6):756-63.

PMID:23997901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3758030/
Abstract

OBJECTIVE(S): Erythropoiesis is regulated by some extrinsic and intrinsic factors as microRNAs (miRNAs). miRNAs are endogenously small non-coding regulatory RNAs which play vital roles in the variety of cellular fate, critical processes; growth, apoptosis, metabolism, survival of the cells and specially differentiation. Several miRNAs such as miR-16 and miR-451 have been shown to be correlated with erythroid differentiation. Taking into account the importance of miRNAs in cellular differentiation, the goal of the present study was to examine the role of miRNAs in hematopoietic stem cells (HSC) differentiation into the erythroid cells in the absence of growth factors and stimulatory cytokines.

MATERIALS AND METHODS

CD133+ stem cells were infected with lentiviruses containing miR-451/miR-16 precursor sequence, erythroid differentiation was evaluated using RT-PCR for hemoglobin chains and surface antigens, also by banzidine staining.

RESULTS

MiR-451up-regulation, but not miR-16, could induce α, β and γ-globin expression in CD133+ cells and have strong correlation with appearance of CD71 and CD235a markers in these cells. Moreover, miR-451 up-regulation increases the banzidine positive cells to ~ %40.

CONCLUSION

Our results provide strong evidence that miR-451 up-regulation strongly induces erythroid differentiation and maturation of CD133+ stem cells. Hence, this method may provide a useful technique for the production of artificial blood RBC and be used as a new strategy for gene therapy of hemoglobinopathies, such as β-thalassemias and sickle cell anemia.

摘要

目的

红细胞生成受一些外在和内在因素的调节,如 microRNAs(miRNAs)。miRNAs 是内源性的小非编码调节 RNA,在细胞命运、关键过程的多样性中发挥重要作用;细胞的生长、凋亡、代谢、存活,特别是分化。一些 miRNAs,如 miR-16 和 miR-451,已被证明与红细胞分化有关。考虑到 miRNAs 在细胞分化中的重要性,本研究的目的是研究在没有生长因子和刺激细胞因子的情况下,miRNAs 在造血干细胞(HSC)向红细胞分化中的作用。

材料和方法

CD133+干细胞被感染含有 miR-451/miR-16 前体序列的慢病毒,使用 RT-PCR 评估血红蛋白链和表面抗原的红细胞分化,也通过碱性品红染色。

结果

miR-451 的上调,但不是 miR-16,可以诱导 CD133+细胞中的α、β和γ-珠蛋白表达,并与这些细胞中 CD71 和 CD235a 标志物的出现有很强的相关性。此外,miR-451 的上调将碱性品红阳性细胞增加到~40%。

结论

我们的结果提供了强有力的证据,表明 miR-451 的上调强烈诱导 CD133+干细胞的红细胞分化和成熟。因此,这种方法可能为人工血液 RBC 的生产提供有用的技术,并可作为血红蛋白病(如β-地中海贫血和镰状细胞贫血)基因治疗的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/b483e697d3ce/ijbms-16-756-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/db4aca0a8808/ijbms-16-756-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/032fef460288/ijbms-16-756-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/e601bf511899/ijbms-16-756-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/b483e697d3ce/ijbms-16-756-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/db4aca0a8808/ijbms-16-756-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/032fef460288/ijbms-16-756-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/e601bf511899/ijbms-16-756-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b67f/3758030/b483e697d3ce/ijbms-16-756-g004.jpg

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