Harvard-MIT Program in Health Sciences and Technology, Harvard Medical School, Boston, Massachusetts, USA; email:
Department of Immunology, Harvard Medical School, Boston, Massachusetts, USA; email:
Annu Rev Cell Dev Biol. 2024 Oct;40(1):283-300. doi: 10.1146/annurev-cellbio-112122-023316. Epub 2024 Sep 21.
Medullary thymic epithelial cells (mTECs) generate immunological self-tolerance by ectopically expressing peripheral-tissue antigens (PTAs) within the thymus to preview the peripheral self to maturing T cells. Recent work, drawing inspiration from old histological observations, has shown that subtypes of mTECs, collectively termed mimetic cells, co-opt developmental programs from throughout the organism to express biologically coherent groups of PTAs. Here, we review key aspects of mimetic cells, especially as they relate to the larger contexts of molecular, cellular, developmental, and evolutionary biology. We highlight lineage-defining transcription factors as key regulators of mimetic cells and speculate as to what other factors, including Aire and the chromatin potential of mTECs, permit mimetic cell differentiation and function. Last, we consider what mimetic cells can teach us about not only the thymus but also other tissues.
髓质胸腺上皮细胞 (mTEC) 通过在外周组织抗原 (PTA) 在胸腺内异位表达,预先展示外周自身给成熟 T 细胞,从而产生免疫自身耐受性。最近的工作从旧的组织学观察中汲取灵感,表明 mTEC 的亚型,统称为模拟细胞,共同采用来自整个生物体的发育程序来表达生物学上一致的 PTA 群。在这里,我们回顾了模拟细胞的关键方面,特别是它们与分子、细胞、发育和进化生物学的更大背景的关系。我们强调谱系定义转录因子作为模拟细胞的关键调节剂,并推测还有哪些其他因素,包括 Aire 和 mTEC 的染色质潜力,允许模拟细胞分化和功能。最后,我们考虑模拟细胞可以教会我们什么,不仅是关于胸腺,还有其他组织。