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T细胞白血病癌蛋白SCL/tal-1对所有造血谱系的发育至关重要。

The T cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages.

作者信息

Porcher C, Swat W, Rockwell K, Fujiwara Y, Alt F W, Orkin S H

机构信息

Division of Hematology and Oncology, Childrens Hospital, Boston, Massachusetts, USA.

出版信息

Cell. 1996 Jul 12;86(1):47-57. doi: 10.1016/s0092-8674(00)80076-8.

Abstract

The T cell leukemia oncoprotein SCL/tal-1, a basic-helix-loop-helix transcription factor, is required for production of embryonic red blood cells in the mouse yolk sac. To define roles in other lineages, we studied the hematopoietic potential of homozygous mutant SCL/tal-1 -/- embryonic stem cells upon in vitro differentiation and in vivo in chimeric mice. Here we show that in the absence of SCL/tal-1, hematopoiesis, Including the generation of red cells, myeloid cells, megakaryocytes, mast cells, and both T and B lymphoid cells, is undetectable. These findings suggest that SCL/tal-1 functions very early in hematopoietic development, either in specification of ventral mesoderm to a blood cell fate, or in formation or maintenance of immature progenitors.

摘要

T细胞白血病癌蛋白SCL/tal-1是一种碱性螺旋-环-螺旋转录因子,是小鼠卵黄囊中胚胎红细胞生成所必需的。为了确定其在其他细胞谱系中的作用,我们研究了纯合突变型SCL/tal-1 -/-胚胎干细胞在体外分化以及在嵌合小鼠体内的造血潜能。我们在此表明,在缺乏SCL/tal-1的情况下,无法检测到造血作用,包括红细胞、髓样细胞、巨核细胞、肥大细胞以及T和B淋巴细胞的生成。这些发现表明,SCL/tal-1在造血发育的早期发挥作用,要么在将腹侧中胚层指定为血细胞命运方面,要么在未成熟祖细胞的形成或维持方面。

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