从鼠胚胎和造血干细胞生成的髓源性抑制细胞的发育和功能。

Development and function of myeloid-derived suppressor cells generated from mouse embryonic and hematopoietic stem cells.

机构信息

Department of Gene and Cell Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

Stem Cells. 2010 Mar 31;28(3):620-32. doi: 10.1002/stem.301.

Abstract

Emerging evidence suggests that myeloid-derived suppressor cells (MDSCs) have great potential as a novel immune intervention modality in the fields of transplantation and autoimmune diseases. Thus far, efforts to develop MDSC-based therapeutic strategies have been hampered by the lack of a reliable source of MDSCs. Here we show that functional MDSCs can be efficiently generated from mouse embryonic stem (ES) cells and bone marrow hematopoietic stem (HS) cells. In vitro-derived MDSCs encompass two homogenous subpopulations: CD115(+)Ly-6C(+) and CD115(+)Ly-6C(-) cells. The CD115(+)Ly-6C(+) subset is equivalent to the monocytic Gr-1(+)CD115(+)F4/80(+) MDSCs found in tumor-bearing mice. In contrast, the CD115(+)Ly-6C(-) cells, a previously unreported population of MDSCs, resemble the granulocyte/macrophage progenitors developmentally. In vitro, ES- and HS-MDSCs exhibit robust suppression against T-cell proliferation induced by polyclonal stimuli or alloantigens via multiple mechanisms involving nitric oxide synthase-mediated NO production and interleukin (IL)-10. Impressively, they display even stronger suppressive activity and significantly enhance ability to induce CD4(+)CD25(+)Foxp3(+) regulatory T-cell development compared with tumor-derived MDSCs. Furthermore, adoptive transfer of ES-MDSCs can effectively prevent alloreactive T-cell-mediated lethal graft-versus-host disease, leading to nearly 82% long-term survival among treated mice. The successful in vitro generation of MDSCs may represent a critical step toward potential clinical application of MDSCs.

摘要

新出现的证据表明,髓系来源的抑制细胞(MDSCs)在移植和自身免疫性疾病领域作为一种新的免疫干预方式具有巨大的潜力。迄今为止,开发基于 MDSC 的治疗策略的努力受到缺乏可靠的 MDSC 来源的阻碍。在这里,我们表明功能齐全的 MDSC 可以从鼠胚胎干细胞(ES 细胞)和骨髓造血干细胞(HS 细胞)中有效地产生。体外衍生的 MDSC 包含两个同质亚群:CD115(+)Ly-6C(+)和 CD115(+)Ly-6C(-)细胞。CD115(+)Ly-6C(+)亚群等同于在荷瘤小鼠中发现的单核细胞 Gr-1(+)CD115(+)F4/80(+)MDSC。相比之下,CD115(+)Ly-6C(-)细胞,一种以前未报道的 MDSC 群体,在发育上类似于粒细胞/巨噬细胞祖细胞。在体外,ES 和 HS-MDSC 通过涉及一氧化氮合酶介导的 NO 产生和白细胞介素(IL)-10 的多种机制,对多克隆刺激物或同种抗原诱导的 T 细胞增殖表现出强大的抑制作用。令人印象深刻的是,与肿瘤衍生的 MDSC 相比,它们显示出更强的抑制活性,并显著增强诱导 CD4(+)CD25(+)Foxp3(+)调节性 T 细胞发育的能力。此外,ES-MDSC 的过继转移可以有效地防止同种反应性 T 细胞介导的致命移植物抗宿主病,导致治疗小鼠中有近 82%的长期存活率。MDSC 的成功体外生成可能是 MDSC 潜在临床应用的关键步骤。

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