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间充质干细胞与 Th17 细胞免疫调节对话背后的机制。

Mechanisms behind the Immunoregulatory Dialogue between Mesenchymal Stem Cells and Th17 Cells.

机构信息

IRMB, University of Montpellier, INSERM, F-34090 Montpellier, France.

IGH, University of Montpellier, CNRS, F-34396 Montpellier, France.

出版信息

Cells. 2020 Jul 10;9(7):1660. doi: 10.3390/cells9071660.

Abstract

Mesenchymal stem cells (MSCs) exhibit potent immunoregulatory abilities by interacting with cells of the adaptive and innate immune system. In vitro, MSCs inhibit the differentiation of T cells into T helper 17 (Th17) cells and repress their proliferation. In vivo, the administration of MSCs to treat various experimental inflammatory and autoimmune diseases, such as rheumatoid arthritis, type 1 diabetes, multiple sclerosis, systemic lupus erythematosus, and bowel disease showed promising therapeutic results. These therapeutic properties mediated by MSCs are associated with an attenuated immune response characterized by a reduced frequency of Th17 cells and the generation of regulatory T cells. In this manuscript, we review how MSC and Th17 cells interact, communicate, and exchange information through different ways such as cell-to-cell contact, secretion of soluble factors, and organelle transfer. Moreover, we discuss the consequences of this dynamic dialogue between MSC and Th17 well described by their phenotypic and functional plasticity.

摘要

间充质干细胞 (MSCs) 通过与适应性和固有免疫系统的细胞相互作用,表现出强大的免疫调节能力。在体外,MSCs 抑制 T 细胞向辅助性 T 细胞 17 (Th17) 细胞的分化,并抑制其增殖。在体内,给予 MSCs 治疗各种实验性炎症和自身免疫性疾病,如类风湿关节炎、1 型糖尿病、多发性硬化症、系统性红斑狼疮和肠道疾病,显示出有希望的治疗效果。MSCs 介导的这些治疗特性与免疫反应减弱有关,其特征是 Th17 细胞的频率降低和调节性 T 细胞的产生。在本文中,我们回顾了 MSC 和 Th17 细胞如何通过细胞间接触、可溶性因子的分泌和细胞器转移等不同方式相互作用、交流和交换信息。此外,我们讨论了这种 MSC 和 Th17 之间动态对话的后果,这些后果很好地描述了它们的表型和功能可塑性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/424c/7408034/1a593562f353/cells-09-01660-g001.jpg

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