Suppr超能文献

E 蛋白和 Id 蛋白控制 T 细胞和先天淋巴细胞命运的分歧。

The divergence between T cell and innate lymphoid cell fates controlled by E and Id proteins.

机构信息

Program in Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, United States.

Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, United States.

出版信息

Front Immunol. 2022 Aug 10;13:960444. doi: 10.3389/fimmu.2022.960444. eCollection 2022.

Abstract

T cells develop in the thymus from lymphoid primed multipotent progenitors or common lymphoid progenitors into αβ and γδ subsets. The basic helix-loop-helix transcription factors, E proteins, play pivotal roles at multiple stages from T cell commitment to maturation. Inhibitors of E proteins, Id2 and Id3, also regulate T cell development while promoting ILC differentiation. Recent findings suggest that the thymus can also produce innate lymphoid cells (ILCs). In this review, we present current findings that suggest the balance between E and Id proteins is likely to be critical for controlling the bifurcation of T cell and ILC fates at early stages of T cell development.

摘要

T 细胞在胸腺中从淋巴样前体多能祖细胞或共同淋巴样祖细胞发育为αβ和γδ亚群。碱性螺旋-环-螺旋转录因子 E 蛋白在 T 细胞的定向到成熟的多个阶段中发挥关键作用。E 蛋白抑制剂 Id2 和 Id3 也调节 T 细胞发育,同时促进 ILC 分化。最近的发现表明,胸腺也可以产生先天淋巴细胞(ILC)。在这篇综述中,我们提出了目前的发现,即 E 和 Id 蛋白之间的平衡可能对控制 T 细胞和 ILC 命运在 T 细胞发育的早期阶段的分叉至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e84/9399370/6097683bbfbd/fimmu-13-960444-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验