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GATA-1而非SCL可诱导早期髓系细胞系向巨核细胞分化。

GATA-1 but not SCL induces megakaryocytic differentiation in an early myeloid line.

作者信息

Visvader J E, Elefanty A G, Strasser A, Adams J M

机构信息

Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.

出版信息

EMBO J. 1992 Dec;11(12):4557-64. doi: 10.1002/j.1460-2075.1992.tb05557.x.

Abstract

GATA-1, a transcription factor of the 'zinc-finger' family, is required for the development of mature erythroid cells and is also highly expressed in the megakaryocytic and mast cell lineages. The helix-loop-helix gene SCL (or TAL) is expressed in the same three hematopoietic lineages as GATA-1. To explore the role of GATA-1 and SCL in hematopoietic differentiation, we introduced a new expression vector bearing each gene into the early myeloid cell line 416B, which could originally differentiate in vivo along the megakaryocytic and granulocytic lineages. Enforced expression of SCL at high levels did not provoke differentiation, but GATA-1 induced the appearance of megakaryocytes as assessed by morphology, the presence of acetylcholinesterase and a polyploid DNA content. Although GATA-1 is thought to stimulate its own transcription in erythrocytes, expression of the endogenous gene was not increased in the megakaryocytic lines; hence GATA-1 may not be autoregulatory in this lineage. Megakaryocytic differentiation was accompanied by a marked decrease in the myeloid surface marker Mac-1. The absence of mast cell or erythroid differentiation suggests that GATA-1 may not be sufficient to provoke maturation along these lineages or that these pathways are impeded in 416B cells. These results demonstrate that a member of the GATA gene family can act as an important regulator of megakaryocytic differentiation.

摘要

GATA-1是“锌指”家族的一种转录因子,是成熟红细胞发育所必需的,在巨核细胞和肥大细胞谱系中也高度表达。螺旋-环-螺旋基因SCL(或TAL)与GATA-1在相同的三种造血谱系中表达。为了探究GATA-1和SCL在造血分化中的作用,我们将携带每个基因的新表达载体导入早期髓系细胞系416B,该细胞系原本在体内可沿巨核细胞和粒细胞谱系分化。高水平强制表达SCL并未引发分化,但通过形态学、乙酰胆碱酯酶的存在及多倍体DNA含量评估,GATA-1诱导了巨核细胞的出现。尽管GATA-1被认为在红细胞中可刺激自身转录,但在巨核细胞系中内源性基因的表达并未增加;因此,GATA-1在该谱系中可能不是自动调节的。巨核细胞分化伴随着髓系表面标志物Mac-1的显著减少。肥大细胞或红细胞分化的缺失表明,GATA-1可能不足以引发这些谱系的成熟,或者这些途径在416B细胞中受到阻碍。这些结果表明,GATA基因家族的一个成员可作为巨核细胞分化的重要调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28bc/557031/13ec377b31b0/emboj00097-0309-a.jpg

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