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通过降低干细胞白血病/T细胞急性白血病1的表达来损害人类普通髓系祖细胞而非粒单核祖细胞的粒单核细胞发育。

Impairment of granulo-monocytic development of human common myeloid progenitors but not of granulo-monocytic progenitors by decreasing stem cell leukemia/T-cell acute leukemia 1 expression.

作者信息

Brunet de la Grange Philippe, Zink Estelle, Armstrong Florence, Rouyez Marie-Christine, Pflumio Françoise

出版信息

Stem Cells. 2008 Jun;26(6):1658-62. doi: 10.1634/stemcells.2007-0952. Epub 2008 Apr 24.

Abstract

We recently showed that Stem Cell Leukemia/T-cell Acute Leukemia 1 (SCL/TAL1) regulates hematopoiesis from hematopoietic stem cells to committed myeloid progenitors compartment. However, in this heterogeneous compartment, the precise role of TAL1, that is largely debated, remains to be clearly defined, notably at the common myeloid progenitor (CMP) and granulo-monocytic progenitor (GMP) levels. Using small hairpin (sh)RNA lentiviral constructs, we decreased TAL1 expression in sorted human CMP and GMP subpopulations that were then assayed for erythroid and granulo-monocytic (GM) differentiation. Decreased TAL1 expression in CMP resulted in rare erythroid colonies, in a 2-3 fold reduction of GM colony number in clonogenic assays and in a 3.6-5.6 decreased production of CD14(+)CD15(+) GM cells in liquid culture. Moreover, analysis of transcript profile of gene involved in GM differentiation showed that GM cells expressing shRNA-TAL1 construct displayed decreased levels of g-csfr, c/ebpalpha, and mpo and high levels of gata-2 transcripts, indicating a blocking of GM differentiation. In contrast, GM differentiation of GMP remained unaffected when TAL1 transcript levels were decreased. These data definitively delineate the human myeloid progenitors that are regulated by TAL1. Disclosure of potential conflicts of interest is found at the end of this article.

摘要

我们最近发现,干细胞白血病/T细胞急性白血病1(SCL/TAL1)可调节从造血干细胞到定向髓系祖细胞区室的造血过程。然而,在这个异质性区室中,TAL1的确切作用在很大程度上存在争议,仍有待明确界定,尤其是在常见髓系祖细胞(CMP)和粒-单核祖细胞(GMP)水平上。我们使用小发夹(sh)RNA慢病毒构建体,降低了分选的人类CMP和GMP亚群中的TAL1表达,随后对这些亚群进行红系和粒-单核(GM)分化检测。CMP中TAL1表达降低导致红系集落罕见,克隆形成试验中GM集落数量减少2-3倍,液体培养中CD14(+)CD15(+)GM细胞的产量降低3.6-5.6倍。此外,对参与GM分化的基因转录谱分析表明,表达shRNA-TAL1构建体的GM细胞显示g-csfr、c/ebpalpha和mpo水平降低,gata-2转录本水平升高,表明GM分化受阻。相比之下,当TAL1转录水平降低时,GMP的GM分化不受影响。这些数据明确界定了受TAL1调控的人类髓系祖细胞。潜在利益冲突的披露见本文末尾。

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