Department of Allergy and Clinical Immunology, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chiba City, 260-8670, Japan.
Laboratory of Medical Omics Research, Kazusa DNA Research Institute, Kamatari, Kisarazu City, 292-0818, Japan.
Sci Rep. 2023 Jan 30;13(1):1653. doi: 10.1038/s41598-023-28987-1.
Epithelial cells control a variety of immune cells by secreting cytokines to maintain tissue homeostasis on mucosal surfaces. Regulatory T (Treg) cells are essential for immune homeostasis and for preventing tissue inflammation; however, the precise molecular mechanisms by which epithelial cell-derived cytokines function on Treg cells in the epithelial tissues are not well understood. Here, we show that peripheral Treg cells preferentially respond to thymic stromal lymphoprotein (TSLP). Although TSLP does not affect thymic Treg differentiation, TSLP receptor-deficient induced Treg cells derived from naïve CD4 T cells are less activated in an adoptive transfer model of colitis. Mechanistically, TSLP activates induced Treg cells partially through mTORC1 activation and fatty acid uptake. Thus, TSLP modulates the activation status of induced Treg through the enhanced uptake of fatty acids to maintain homeostasis in the large intestine.
上皮细胞通过分泌细胞因子来控制各种免疫细胞,以维持黏膜表面的组织稳态。调节性 T(Treg)细胞对于免疫稳态和防止组织炎症至关重要;然而,上皮细胞衍生的细胞因子在上皮组织中的 Treg 细胞上发挥作用的确切分子机制尚不清楚。在这里,我们表明外周 Treg 细胞优先对胸腺基质淋巴细胞生成素(TSLP)作出反应。尽管 TSLP 不影响胸腺 Treg 分化,但从幼稚 CD4 T 细胞中衍生的 TSLP 受体缺陷型诱导性 Treg 细胞在结肠炎的过继转移模型中激活程度较低。从机制上讲,TSLP 通过 mTORC1 激活和脂肪酸摄取部分激活诱导性 Treg 细胞。因此,TSLP 通过增强脂肪酸摄取来调节诱导性 Treg 的激活状态,以维持大肠的稳态。