Department of Immunology, Biomedical Science Tower, University of Pittsburgh, Pittsburgh, PA, USA.
Immunology. 2018 Feb;153(2):238-245. doi: 10.1111/imm.12836. Epub 2017 Oct 5.
Invariant natural killer T (iNKT) cells are adaptive T cells with innate-like characteristics including rapid cytokine production and a proliferative response to stimulation. Development of these cells in the thymus is dependent on expression of the microRNA (miRNA) processing enzyme Dicer, indicating that iNKT cells probably have distinct miRNA requirements for gene regulation during development. The miRNA miR-155 has previously been shown to have numerous roles in T cells, including regulation of proliferation and differentiation, and positive modulation of interferon-γ expression. We examined the role of miR-155 in the development and function of iNKT cells. Using germline-deficient miR-155 mice, we showed that loss of miR-155 resulted in unchanged iNKT cell frequency and cell number. Although miR-155 was up-regulated in iNKT cells upon activation with α-galactosylceramide, loss of miR-155 did not affect cytokine production or proliferation by iNKT cells. Hence, cytokine production occurs in iNKT cells independently of miR-155 expression.
不变自然杀伤 T(iNKT)细胞是具有先天样特征的适应性 T 细胞,包括快速细胞因子产生和对刺激的增殖反应。这些细胞在胸腺中的发育依赖于微 RNA(miRNA)加工酶 Dicer 的表达,表明 iNKT 细胞在发育过程中可能具有独特的 miRNA 基因调控要求。miR-155 先前已被证明在 T 细胞中具有多种作用,包括调节增殖和分化,以及正向调节干扰素-γ表达。我们研究了 miR-155 在 iNKT 细胞发育和功能中的作用。使用种系缺失 miR-155 的小鼠,我们表明 miR-155 的缺失导致 iNKT 细胞频率和数量不变。尽管用α-半乳糖神经酰胺激活时 iNKT 细胞中 miR-155 上调,但 miR-155 的缺失并不影响 iNKT 细胞的细胞因子产生或增殖。因此,细胞因子的产生发生在 iNKT 细胞中,而不依赖于 miR-155 的表达。