Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Division of Hematology and Oncology, Department of Medicine, Freiburg University Medical Center, Albert-Ludwigs-University, 79106 Freiburg, Germany.
Sci Immunol. 2018 Jan 12;3(19). doi: 10.1126/sciimmunol.aal2736.
The thymus is not only extremely sensitive to damage but also has a remarkable ability to repair itself. However, the mechanisms underlying this endogenous regeneration remain poorly understood, and this capacity diminishes considerably with age. We show that thymic endothelial cells (ECs) comprise a critical pathway of regeneration via their production of bone morphogenetic protein 4 (BMP4) ECs increased their production of BMP4 after thymic damage, and abrogating BMP4 signaling or production by either pharmacologic or genetic inhibition impaired thymic repair. EC-derived BMP4 acted on thymic epithelial cells (TECs) to increase their expression of , a key transcription factor involved in TEC development, maintenance, and regeneration, and its downstream targets such as , a key mediator of thymocyte development and regeneration. These studies demonstrate the importance of the BMP4 pathway in endogenous tissue regeneration and offer a potential clinical approach to enhance T cell immunity.
胸腺不仅对损伤极其敏感,而且具有显著的自我修复能力。然而,这种内源性再生的机制仍知之甚少,而且这种能力随着年龄的增长而大大降低。我们发现,胸腺内皮细胞(ECs)通过其产生的骨形态发生蛋白 4(BMP4)构成了再生的关键途径。ECs 在胸腺损伤后增加了 BMP4 的产生,而通过药理学或遗传抑制来阻断 BMP4 信号或产生会损害胸腺修复。EC 衍生的 BMP4 作用于胸腺上皮细胞(TECs),增加其关键转录因子的表达,该转录因子参与 TEC 的发育、维持和再生,以及其下游靶标,如 ,它是胸腺细胞发育和再生的关键介质。这些研究表明 BMP4 途径在体内组织再生中的重要性,并为增强 T 细胞免疫提供了一种潜在的临床方法。