Bartemes Kathleen, Chen Chien-Chang, Iijima Koji, Drake Li, Kita Hirohito
Division of Allergic Diseases, Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905; and.
Department of Immunology, Mayo Clinic, Rochester, MN 55905.
J Immunol. 2018 Jan 1;200(1):229-236. doi: 10.4049/jimmunol.1602085. Epub 2017 Nov 13.
Group 2 innate lymphoid cells (ILC2s) reside in multiple organs in the body, where they play roles in immunity, tissue homeostasis, and metabolic regulation. However, little is known about the regulatory mechanisms of ILC2s in different organs. Here, we identified ILC2s in the mouse uterus and found that they express cell surface molecules, including the IL-33 receptor, ST2, that are roughly comparable to those expressed by lung ILC2s. Both in vivo and in vitro treatment with IL-33 induced type 2 cytokine production in uterine ILC2s, suggesting that they respond to IL-33 in a manner similar to ILC2s in other organs. Importantly, uterine ILC2s were nearly absent in ovariectomized mice and were increased in wild-type mice by estrogen administration, whereas lung ILC2s were unaffected by both ovariectomy and estrogen administration. Likewise, a marked reduction in uterine ILC2s was observed in mice deficient in estrogen receptor α or estrogen receptor β. Furthermore, uterine ILC2s highly expressed estrogen receptor α, and in vitro culture of isolated uterine ILC2s with 17β-estradiol modified expression of a number of genes. Finally, an increased prevalence in neonatal mortality was observed in litters from dams lacking the IL-33 receptor, ST2. Taken together, our findings indicate that unlike lung IL2Cs, uterine ILC2s are regulated by female sex hormones, which may specialize them for specific physiological functions.
第2组固有淋巴细胞(ILC2s)存在于身体的多个器官中,在免疫、组织稳态和代谢调节中发挥作用。然而,关于ILC2s在不同器官中的调节机制知之甚少。在此,我们在小鼠子宫中鉴定出ILC2s,并发现它们表达细胞表面分子,包括IL-33受体ST2,其表达情况与肺ILC2s大致相当。体内和体外给予IL-33均能诱导子宫ILC2s产生2型细胞因子,这表明它们对IL-33的反应方式与其他器官中的ILC2s相似。重要的是,去卵巢小鼠的子宫ILC2s几乎缺失,而野生型小鼠经雌激素处理后子宫ILC2s增加,而肺ILC2s不受去卵巢和雌激素处理的影响。同样,在雌激素受体α或雌激素受体β缺陷的小鼠中观察到子宫ILC2s明显减少。此外,子宫ILC2s高度表达雌激素受体α,用17β-雌二醇对分离出的子宫ILC2s进行体外培养可改变许多基因的表达。最后,在缺乏IL-33受体ST2的母鼠所产的幼崽中观察到新生儿死亡率增加。综上所述,我们的研究结果表明,与肺ILC2s不同,子宫ILC2s受女性性激素调节,这可能使它们具有特定的生理功能。