Ma Lisa J, Acero Luis F, Zal Tomasz, Schluns Kimberly S
Department of Immunology, University of Texas M.D. Anderson Cancer Center, Houston, Texas 77030, USA.
J Immunol. 2009 Jul 15;183(2):1044-54. doi: 10.4049/jimmunol.0900420. Epub 2009 Jun 24.
IL-15 is crucial for the development of intestinal intraepithelial lymphocytes (IEL) and delivery is mediated by a unique mechanism known as trans-presentation. Parenchymal cells have a major role in the trans-presentation of IL-15 to IELs, but the specific identity of this cell type is unknown. To investigate whether the intestinal epithelial cells (IEC) are the parenchymal cell type involved, a mouse model that expresses IL-15Ralpha exclusively by the IECs (Villin/IL-15Ralpha Tg) was generated. Exclusive expression of IL-15Ralpha by the IECs restored all the deficiencies in the CD8alphaalpha(+)TCRalphabeta(+)and CD8alphaalpha(+)TCRgammadelta(+) subsets that exist in the absence of IL-15Ralpha. Interestingly, most of the IEL recovery was due to the preferential increase in Thy1(low) IELs, which compose a majority of the IEL population. The differentiation of Thy1(high)CD4(-)CD8(-) thymocytes into Thy1(-)CD8alphaalpha IELs was found to require IL-15Ralpha expression specifically by IECs and thus, provides evidence that differentiation of Thy1(low) IELs is one function of trans-presentation of IL-15 in the intestines. In addition to effects in IEL differentiation, trans-presentation of IL-15 by IECs also resulted in an increase in IEL numbers that was accompanied by increases in Bcl-2, but not proliferation. Collectively, this study demonstrates that trans-presentation of IL-15 by IECs alone is completely sufficient to direct the IL-15-mediated development of CD8alphaalpha(+) T cell populations within the IEL compartment, which now includes a newly identified role of IL-15 in the differentiation of Thy1(low) IELs.
白细胞介素-15(IL-15)对肠道上皮内淋巴细胞(IEL)的发育至关重要,其传递由一种称为反式呈递的独特机制介导。实质细胞在将IL-15反式呈递给IEL的过程中起主要作用,但这种细胞类型的具体身份尚不清楚。为了研究肠道上皮细胞(IEC)是否是所涉及的实质细胞类型,构建了一种仅由IEC表达IL-15Rα的小鼠模型(Villin/IL-15Rα Tg)。IEC对IL-15Rα的特异性表达恢复了在缺乏IL-15Rα时CD8αα(+)TCRαβ(+)和CD8αα(+)TCRγδ(+)亚群中存在的所有缺陷。有趣的是,大多数IEL的恢复归因于Thy1(low) IEL的优先增加,Thy1(low) IEL构成了IEL群体的大部分。发现Thy1(high)CD4(-)CD8(-)胸腺细胞向Thy1(-)CD8αα IEL的分化特别需要IEC表达IL-15Rα,因此,这提供了证据表明Thy1(low) IEL的分化是肠道中IL-15反式呈递的一项功能。除了对IEL分化的影响外,IEC对IL-15的反式呈递还导致IEL数量增加,同时Bcl-2增加,但没有增殖。总的来说,这项研究表明,仅IEC对IL-15的反式呈递就完全足以指导IEL区室中IL-15介导的CD8αα(+) T细胞群体的发育,这现在包括IL-15在Thy1(low) IEL分化中的新确定作用。