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在微生物的世界中,RORγt+ 细胞的发育和演化。

Development and evolution of RORγt+ cells in a microbe's world.

机构信息

Lymphoid Tissue Development Unit, Institut Pasteur, Paris, France. CNRS, URA1961, Paris, France.

出版信息

Immunol Rev. 2012 Jan;245(1):177-88. doi: 10.1111/j.1600-065X.2011.01071.x.

Abstract

The nuclear hormone receptor retinoid-related orphan receptor γt (RORγt) induces a pro-inflammatory program in lymphoid cells, culminating in the expression of interleukin-6 (IL-6), IL-17, IL-22, granulocyte-macrophage colony-stimulating factor, and tumor necrosis factor. During ontogeny, the first type of cells expressing RORγt are lymphoid tissue inducer cells, a type of innate lymphoid cell (ILC) generated in mammalian fetuses to induce the development of lymph nodes and Peyer's patches. After birth, RORγt(+) ILCs and RORγt(+) T cells are involved in the defense of epithelial surfaces against extracellular microbes and play an important role in the intestinal homeostasis with symbiotic microbiota. The development and evolution of RORγt(+) cells is intimately associated with the construction of a stable host-microbe interface.

摘要

核激素受体视黄酸相关孤儿受体 γt(RORγt)在淋巴细胞中诱导促炎程序,最终导致白细胞介素-6(IL-6)、IL-17、IL-22、粒细胞-巨噬细胞集落刺激因子和肿瘤坏死因子的表达。在个体发生过程中,表达 RORγt 的第一类细胞是淋巴组织诱导细胞,这是一种在哺乳动物胎儿中产生的固有淋巴细胞(ILC),用于诱导淋巴结和派尔集合淋巴结的发育。出生后,RORγt(+) ILC 和 RORγt(+) T 细胞参与抵抗上皮表面的细胞外微生物,并在与共生微生物的肠道平衡中发挥重要作用。RORγt(+)细胞的发育和进化与稳定的宿主-微生物界面的构建密切相关。

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