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转录因子 Lyl-1 调节淋巴样细胞的特异性和早期 T 细胞谱系祖细胞的维持。

The transcription factor Lyl-1 regulates lymphoid specification and the maintenance of early T lineage progenitors.

机构信息

Department of Haematology, Oncology and Clinical Immunology, Heinrich-Heine-University, Düsseldorf, Germany.

出版信息

Nat Immunol. 2012 Jul 8;13(8):761-9. doi: 10.1038/ni.2365.

Abstract

Thymopoiesis depends on the recruitment and expansion of bone marrow-derived progenitor populations; tight regulation of these processes is required for maintenance of the homeostasis of the T lineage. Lyl-1, a transcription factor that regulates hematopoietic progenitors, is expressed in thymocyte progenitors until T cell commitment. Here we demonstrate a requirement for Lyl-1 in lymphoid specification and the maintenance of early T lineage progenitors (ETPs). Lyl-1 deficiency resulted in profound defects in the generation of lymphoid-primed multipotent progenitors (LMPPs), common lymphoid progenitors (CLPs) and ETPs. Lyl-1-deficient ETPs and thymocyte progenitors at the CD4(-)CD8(-) double-negative 2 (DN2) stage showed more apoptosis, blocked differentiation and impaired population expansion. We identified Gfi1 as a critical transcriptional target of Lyl-1-mediated lymphopoiesis of T cells. Thus, Lyl-1 is a pivotal component of a transcriptional program that controls the lymphoid specification and maintenance of ETPs.

摘要

胸腺生成依赖于骨髓来源的祖细胞群体的募集和扩增;这些过程的紧密调节对于 T 细胞谱系的稳态维持是必需的。Lyl-1 是一种调节造血祖细胞的转录因子,在胸腺细胞祖细胞中表达,直到 T 细胞承诺。在这里,我们证明了 Lyl-1 在淋巴样特异性和早期 T 谱系祖细胞(ETP)的维持中的必要性。Lyl-1 缺陷导致淋巴样前多能祖细胞(LMPP)、共同淋巴祖细胞(CLP)和 ETP 的生成严重缺陷。Lyl-1 缺陷的 ETP 和 CD4(-)CD8(-)双阴性 2(DN2)阶段的胸腺细胞祖细胞表现出更多的细胞凋亡、分化阻滞和群体扩增受损。我们确定了 Gfi1 作为 Lyl-1 介导的 T 细胞淋巴生成的关键转录靶标。因此,Lyl-1 是控制淋巴样特异性和 ETP 维持的转录程序的关键组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c09/3411897/0d8875c11156/nihms382862f1.jpg

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