Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Eur J Immunol. 2010 Nov;40(11):3210-9. doi: 10.1002/eji.201040699. Epub 2010 Oct 27.
The Src family kinase Lck is thought to facilitate Th2 differentiation; however, its role in Th1 cells has not been well explored. Using mice that lack Lck in mature T cells, we find that lck(-/-) Th1 skewed cells have normal expression of T-bet and produce IFN-γ at WT levels. However, there is a 3-fold increase in IL-10 producing cells in the mutant cultures. These cells do not have elevated levels of IL-4, GATA3, IL-17 or Foxp3, indicating that they are not Th2, Th17, or Foxp3(+) T regulatory cells (Treg). Nor do these cells behave in a similar manner as the type 1 Treg. Most of the IL-10 in the lck(-/-) Th1 cultures is derived from the memory/activated subset, as the cytokine profile from Th1 cultures established from purified CD62L(+) (naïve) cells are similar to WT cells. Furthermore, this IL-10 expression appears to be dependent on IL-12 and correlates with elevated c-Maf. These data highlight a previously unappreciated role for Lck in regulating IL-10 in Th1 cells.
Src 家族激酶 Lck 被认为有助于 Th2 分化;然而,其在 Th1 细胞中的作用尚未得到充分探索。利用成熟 T 细胞中缺乏 Lck 的小鼠,我们发现 lck(-/-)Th1 偏向细胞具有正常的 T-bet 表达,并以 WT 水平产生 IFN-γ。然而,突变培养物中产生 IL-10 的细胞增加了 3 倍。这些细胞没有升高的 IL-4、GATA3、IL-17 或 Foxp3 水平,表明它们不是 Th2、Th17 或 Foxp3(+)T 调节细胞(Treg)。这些细胞的行为也与 1 型 Treg 不同。lck(-/-)Th1 培养物中的大部分 IL-10 来自记忆/激活亚群,因为从纯化的 CD62L(+)(幼稚)细胞建立的 Th1 培养物的细胞因子谱与 WT 细胞相似。此外,这种 IL-10 表达似乎依赖于 IL-12 并与升高的 c-Maf 相关。这些数据突出了 Lck 在调节 Th1 细胞中 IL-10 方面的先前未被重视的作用。