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鉴定人类髓系发生的 microRNA 决定因素。

Identifying microRNA determinants of human myelopoiesis.

机构信息

Gene & Stem Cell Therapy Program, Centenary Institute, University of Sydney, Camperdown, 2050, Australia.

Sydney Medical School, University of Sydney, Sydney, NSW 2006, Australia.

出版信息

Sci Rep. 2018 May 8;8(1):7264. doi: 10.1038/s41598-018-24203-7.

DOI:10.1038/s41598-018-24203-7
PMID:29739970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5940821/
Abstract

Myelopoiesis involves differentiation of hematopoietic stem cells to cellular populations that are restricted in their self-renewal capacity, beginning with the common myeloid progenitor (CMP) and leading to mature cells including monocytes and granulocytes. This complex process is regulated by various extracellular and intracellular signals including microRNAs (miRNAs). We characterised the miRNA profile of human CD34CD38 myeloid progenitor cells, and mature monocytes and granulocytes isolated from cord blood using TaqMan Low Density Arrays. We identified 19 miRNAs that increased in both cell types relative to the CMP and 27 that decreased. miR-125b and miR-10a were decreased by 10-fold and 100-fold respectively in the mature cells. Using in vitro granulopoietic differentiation of human CD34 cells we show that decreases in both miR-125b and miR-10a correlate with a loss of CD34 expression and gain of CD11b and CD15 expression. Candidate target mRNAs were identified by co-incident predictions between the miRanda algorithm and genes with increased expression during differentiation. Using luciferase assays we confirmed MCL1 and FUT4 as targets of miR-125b and the transcription factor KLF4 as a target of miR-10a. Together, our data identify miRNAs with differential expression during myeloid development and reveal some relevant miRNA-target pairs that may contribute to physiological differentiation.

摘要

造血发生涉及造血干细胞向细胞群体的分化,这些细胞群体的自我更新能力受到限制,从共同髓系祖细胞(CMP)开始,最终分化为成熟细胞,包括单核细胞和粒细胞。这个复杂的过程受到各种细胞外和细胞内信号的调节,包括 microRNAs(miRNAs)。我们使用 TaqMan 低密度阵列,对来自脐带血的人 CD34CD38 髓系祖细胞和成熟单核细胞和粒细胞进行了 miRNA 谱分析。我们确定了 19 种在两种细胞类型中相对于 CMP 增加的 miRNA,以及 27 种减少的 miRNA。miR-125b 和 miR-10a 在成熟细胞中分别减少了 10 倍和 100 倍。通过体外人 CD34 细胞的粒系分化,我们表明 miR-125b 和 miR-10a 的减少与 CD34 表达的丧失以及 CD11b 和 CD15 表达的获得相关。通过 miRanda 算法和分化过程中表达增加的基因之间的一致预测,确定了候选靶 mRNA。通过荧光素酶测定法,我们证实了 MCL1 和 FUT4 是 miR-125b 的靶标,转录因子 KLF4 是 miR-10a 的靶标。总之,我们的数据确定了在髓系发育过程中差异表达的 miRNAs,并揭示了一些可能有助于生理分化的相关 miRNA-靶对。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/baa50c05355f/41598_2018_24203_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/478ed7215657/41598_2018_24203_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/2997e989fc2d/41598_2018_24203_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/d010ee9cb2e3/41598_2018_24203_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/109623d79c0c/41598_2018_24203_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/bd742d8b1c91/41598_2018_24203_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/baa50c05355f/41598_2018_24203_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/478ed7215657/41598_2018_24203_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/2997e989fc2d/41598_2018_24203_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/d010ee9cb2e3/41598_2018_24203_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/109623d79c0c/41598_2018_24203_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/bd742d8b1c91/41598_2018_24203_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a472/5940821/baa50c05355f/41598_2018_24203_Fig6_HTML.jpg

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