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停止造血中的切块:我们学到了什么?

Stop the dicing in hematopoiesis: what have we learned?

机构信息

Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.

出版信息

Cell Cycle. 2012 Aug 1;11(15):2799-807. doi: 10.4161/cc.21077.

DOI:10.4161/cc.21077
PMID:22801545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3419058/
Abstract

MicroRNAs (miRNAs) belong to an abundant class of highly conserved small (22nt) non-coding RNAs. MiRNA profiling studies indicate that their expression is highly cell type-dependent. DICER1 is an essential RNase III endoribonuclease for miRNA processing. Hematopoietic cell type- and developmental stage-specific Dicer1 deletion models show that miRNAs are essential regulators of cellular survival, differentiation and function. For instance, miRNA deficiency in hematopoietic stem cells and progenitors of different origins results in decreased cell survival, dramatic developmental aberrations or dysfunctions in mice. We recently found that homozygous Dicer1 deletion in myeloid-committed progenitors results in an aberrant expression of stem cell genes and induces a regained self-renewal capacity. Moreover, Dicer1 deletion causes a block in macrophage development and myeloid dysplasia, a cellular condition that may be considered as a preleukemic state. However, Dicer1-null cells do not develop leukemia in mice, indicating that depletion of miRNAs is not enough for tumorigenesis. Surprisingly, we found that heterozygous Dicer1 deletion in myeloid-committed progenitors, but not Dicer1 knockout, collaborates with p53 deletion in leukemic progression and results in various types of leukemia. Our data indicate that Dicer1 is a haploinsufficient tumorsuppressor in hematopoietic neoplasms, which is consistent with the observed downregulation of miRNA expression in human leukemia samples. Here, we review the various hematopoietic specific Dicer1 deletion mouse models and the phenotypes observed within the different hematopoietic lineages and cell developmental stages. Finally, we discuss the role for DICER1 in mouse and human malignant hematopoiesis.

摘要

MicroRNAs (miRNAs) 属于一类丰富的高度保守的小 (22nt) 非编码 RNA。miRNA 谱分析研究表明,它们的表达高度依赖于细胞类型。DICER1 是 miRNA 加工所必需的 RNase III 内切核酸酶。造血细胞类型和发育阶段特异性 Dicer1 缺失模型表明,miRNAs 是细胞存活、分化和功能的重要调节因子。例如,不同来源的造血干细胞和祖细胞中 miRNA 的缺乏会导致细胞存活减少、发育异常或功能障碍。我们最近发现,髓系定向祖细胞中的 Dicer1 纯合缺失会导致干细胞基因的异常表达,并诱导恢复自我更新能力。此外,Dicer1 缺失会导致巨噬细胞发育和骨髓增生异常,这是一种可能被认为是白血病前状态的细胞状态。然而,Dicer1 缺失的细胞在小鼠中不会发展为白血病,这表明 miRNA 的耗竭不足以导致肿瘤发生。令人惊讶的是,我们发现髓系定向祖细胞中的杂合 Dicer1 缺失,而不是 Dicer1 敲除,与 p53 缺失协同作用,促进白血病的进展,并导致各种类型的白血病。我们的数据表明,Dicer1 是造血肿瘤中的一个半合子肿瘤抑制因子,这与在人类白血病样本中观察到的 miRNA 表达下调相一致。在这里,我们综述了各种造血特异性 Dicer1 缺失小鼠模型以及在不同造血谱系和细胞发育阶段观察到的表型。最后,我们讨论了 DICER1 在小鼠和人类恶性造血中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/2135d80b04aa/cc-11-2799-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/a753780e03d3/cc-11-2799-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/6fb355ccc3ed/cc-11-2799-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/4cd0980f33d8/cc-11-2799-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/2135d80b04aa/cc-11-2799-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/a753780e03d3/cc-11-2799-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/6fb355ccc3ed/cc-11-2799-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/4cd0980f33d8/cc-11-2799-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d0f/3419058/2135d80b04aa/cc-11-2799-g4.jpg

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本文引用的文献

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