谱系(遗传)
减压
转录因子
转分化
生物
B细胞
细胞生物学
细胞
细胞命运测定
转录调控
调节器
遗传学
基因
心理压抑
基因表达
抗体
作者
Kalina T. Belcheva,Jayanta Chaudhuri
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2022-12-01
卷期号:209 (11): 2073-2081
被引量:1
标识
DOI:10.4049/jimmunol.2200497
摘要
The maintenance of B cell identity requires active transcriptional control that enforces a B cell-specific program and suppresses alternative lineage genes. Accordingly, disrupting the B cell identity regulatory network compromises B cell function and induces cell fate plasticity by allowing derepression of alternative lineage-specific transcriptional programs. Although the B lineage is incredibly resistant to most differentiating factors, loss of just a single B lineage-specific transcription factor or the forced expression of individual non-B cell lineage transcription factors can radically disrupt B cell maintenance and allow dedifferentiation or transdifferentiation into entirely distinct lineages. B lymphocytes thereby offer an insightful and useful case study of how a specific cell lineage can maintain a stable identity throughout life and how perturbations of a single master regulator can induce cellular plasticity. In this article, we review the regulatory mechanisms that safeguard B cell identity, and we discuss how dysregulation of the B cell maintenance program can drive malignant transformation and enable therapeutic resistance.
科研通智能强力驱动
Strongly Powered by AbleSci AI