Helix-Loop-Helix Proteins in Adaptive Immune Development

被引:0
|
作者
Aubrey, Megan [1 ]
Warburg, Zachary J. [1 ]
Murre, Cornelis [1 ]
机构
[1] Univ Calif San Diego, Div Biol Sci, Sect Mol Biol, San Diego, CA USA
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
HLH; E proteins; Id proteins; VDJ recombination; lymphopoiesis; hematopoiesis; T cell development; B cell development; TRANSCRIPTION FACTORS E2A; ADULT HEMATOPOIETIC STEM; B-CELL DEVELOPMENT; RECOMBINATION ACTIVATING GENE; LIGHT-CHAIN RECOMBINATION; HEAVY-CHAIN; V(D)J RECOMBINATION; ALPHA-BETA; GERMINAL CENTER; DNA-BINDING;
D O I
10.3389/fimmu.2022.881656
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The E/ID protein axis is instrumental for defining the developmental progression and functions of hematopoietic cells. The E proteins are dimeric transcription factors that activate gene expression programs and coordinate changes in chromatin organization. Id proteins are antagonists of E protein activity. Relative levels of E/Id proteins are modulated throughout hematopoietic development to enable the progression of hematopoietic stem cells into multiple adaptive and innate immune lineages including natural killer cells, B cells and T cells. In early progenitors, the E proteins promote commitment to the T and B cell lineages by orchestrating lineage specific programs of gene expression and regulating VDJ recombination of antigen receptor loci. In mature B cells, the E/Id protein axis functions to promote class switch recombination and somatic hypermutation. E protein activity further regulates differentiation into distinct CD4+ and CD8+ T cells subsets and instructs mature T cell immune responses. In this review, we discuss how the E/Id proteins define the adaptive immune system lineages, focusing on their role in directing developmental gene programs.
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页数:17
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