Fehniger T A, Suzuki K, Ponnappan A, VanDeusen J B, Cooper M A, Florea S M, Freud A G, Robinson M L, Durbin J, Caligiuri M A
Department of Internal Medicine, The Ohio State University, Columbus, Ohio 43210, USA.
J Exp Med. 2001 Jan 15;193(2):219-31. doi: 10.1084/jem.193.2.219.
Inflammation likely has a role in the early genesis of certain malignancies. Interleukin (IL)-15, a proinflammatory cytokine and growth factor, is required for lymphocyte homeostasis. Intriguingly, the expression of IL-15 protein is tightly controlled by multiple posttranscriptional mechanisms. Here, we engineered a transgenic mouse to overexpress IL-15 by eliminating these posttranscriptional checkpoints. IL-15 transgenic mice have early expansions in natural killer (NK) and CD8+ T lymphocytes. Later, these mice develop fatal lymphocytic leukemia with a T-NK phenotype. These data provide novel evidence that leukemia, like certain other cancers, can arise as the result of chronic stimulation by a proinflammatory cytokine.
炎症可能在某些恶性肿瘤的早期发生过程中起作用。白细胞介素(IL)-15是一种促炎细胞因子和生长因子,是淋巴细胞稳态所必需的。有趣的是,IL-15蛋白的表达受到多种转录后机制的严格控制。在此,我们通过消除这些转录后检查点,构建了一种过表达IL-15的转基因小鼠。IL-15转基因小鼠的自然杀伤(NK)细胞和CD8 + T淋巴细胞早期扩增。随后,这些小鼠发展为具有T-NK表型的致命性淋巴细胞白血病。这些数据提供了新的证据,表明白血病与某些其他癌症一样,可能是由促炎细胞因子的慢性刺激导致的。