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Foxn1的一个结构域,其对于依赖串扰的胸腺上皮细胞分化是必需的。

A domain of Foxn1 required for crosstalk-dependent thymic epithelial cell differentiation.

作者信息

Su Dong-ming, Navarre Samuel, Oh Won-jong, Condie Brian G, Manley Nancy R

机构信息

Department of Genetics, Life Sciences Building, University of Georgia, Athens, Georgia 30602, USA.

出版信息

Nat Immunol. 2003 Nov;4(11):1128-35. doi: 10.1038/ni983. Epub 2003 Oct 5.

Abstract

Thymic epithelial cells (TECs) are required for T cell maturation within the thymus. In the nude (Foxn1(nu/nu)) mouse, TECs fail to differentiate. We have generated a hypomorphic allele called Foxn1(Delta), from which an N-terminal domain was deleted. The phenotype was thymus specific, identifying a tissue-specific activity for this domain. Foxn1(Delta/Delta) mice showed abnormal thymic architecture, lacking cortical and medullary domains. In contrast to thymi in mice with the null allele, the Foxn1(Delta/Delta) thymus promoted T cell development, but with specific defects at both the double-negative and double-positive stages. Thus, initiation and progression of TEC differentiation are genetically separable functions of Foxn1, and the N-terminal domain is required for crosstalk-dependent TEC differentiation.

摘要

胸腺上皮细胞(TECs)是胸腺内T细胞成熟所必需的。在裸鼠(Foxn1(nu/nu))中,TECs无法分化。我们产生了一个名为Foxn1(Delta)的低表达等位基因,其N端结构域被删除。该表型具有胸腺特异性,表明该结构域具有组织特异性活性。Foxn1(Delta/Delta)小鼠表现出异常的胸腺结构,缺乏皮质和髓质区域。与具有无效等位基因的小鼠的胸腺不同,Foxn1(Delta/Delta)胸腺促进T细胞发育,但在双阴性和双阳性阶段均存在特定缺陷。因此,TEC分化的起始和进展是Foxn1的遗传可分离功能,N端结构域是串扰依赖性TEC分化所必需的。

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