Walter and Eliza Hall Institute of Medical Research , Parkville, Australia.
Department of Medical Biology, University of Melbourne , Parkville, Australia.
J Exp Med. 2023 Jun 5;220(6). doi: 10.1084/jem.20212383. Epub 2023 Mar 15.
Cell competition has recently emerged as an important tumor suppressor mechanism in the thymus that inhibits autonomous thymic maintenance. Here, we show that the oncogenic transcription factor Lmo2 causes autonomous thymic maintenance in transgenic mice by inhibiting early T cell differentiation. This autonomous thymic maintenance results in the development of self-renewing preleukemic stem cells (pre-LSCs) and subsequent leukemogenesis, both of which are profoundly inhibited by restoration of thymic competition or expression of the antiapoptotic factor BCL2. Genomic analyses revealed the presence of Notch1 mutations in pre-LSCs before subsequent loss of tumor suppressors promotes the transition to overt leukemogenesis. These studies demonstrate a critical role for impaired cell competition in the development of pre-LSCs in a transgenic mouse model of T cell acute lymphoblastic leukemia (T-ALL), implying that this process plays a role in the ontogeny of human T-ALL.
细胞竞争最近被发现是一种重要的胸腺肿瘤抑制机制,可抑制自主胸腺维持。在这里,我们表明,致癌转录因子 Lmo2 通过抑制早期 T 细胞分化,导致转基因小鼠中的自主胸腺维持。这种自主的胸腺维持导致自我更新的前白血病干细胞(pre-LSCs)的发展和随后的白血病发生,而这两者都被恢复胸腺竞争或表达抗凋亡因子 BCL2 所强烈抑制。基因组分析显示,在随后丢失肿瘤抑制基因之前,pre-LSCs 中存在 Notch1 突变,从而促进向显性白血病的转化。这些研究表明,在 T 细胞急性淋巴细胞白血病(T-ALL)的转基因小鼠模型中,受损的细胞竞争在 pre-LSCs 的发展中起关键作用,暗示该过程在人类 T-ALL 的发生中起作用。