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Fms-样酪氨酸激酶 3 配体有助于 CD8 / TCR 辅助细胞中 CD8α 浆细胞样前体细胞树突状细胞亚群的发育和功能。

Fms-Like Tyrosine Kinase 3-Ligand Contributes to the Development and Function of the Subpopulation of CD8α Plasmacytoid Precursor Dendritic Cells in CD8 /TCR Facilitating Cells.

机构信息

Institute for Cellular Therapeutics, University of Louisville, Louisville, Kentucky, USA.

出版信息

Stem Cells. 2018 Oct;36(10):1567-1577. doi: 10.1002/stem.2887. Epub 2018 Jul 29.

DOI:10.1002/stem.2887
PMID:30004616
Abstract

Facilitating cells (FC) are a CD8 TCR bone marrow subpopulation that enhance engraftment of purified hematopoietic stem cells (HSC) and induce antigen-specific CD4 CD25 FoxP3 regulatory T cell (Treg) in vivo. The major subpopulation in FC resembles plasmacytoid precursor dendritic cells (p-preDC) both phenotypically and functionally. Here, we report that the number of FC was significantly reduced in Fms-like tyrosine kinase 3-ligand-knockout (Flt3-L-KO) mice. Specifically, there was a selective decrease in the B220 CD11c CD11b p-preDC FC subpopulation. The p-preDC FC subpopulation in FC total is restored after Flt3-L administration to Flt3-L-KO mice. FC from Flt3-L-KO donors exhibit impaired facilitation of allogeneic HSC engraftment in ablatively conditioned mice (B6 → NOD) as well as in mice conditioned with reduced intensity conditioning (B6 → BALB/c). In addition, the number of CD4 CD25 Foxp3 Treg from Flt3-L-KO mice is significantly decreased. This was associated with the expression of chemokine receptor CXCR3 or CCR5 on Treg. Treg from the spleen of Flt3-L-KO mice showed impaired facilitation of engraftment of allogeneic HSC compared to wild-type Treg. Flt3-L treatment significantly expanded Treg, and restored their facilitating function. These results suggest that Flt3-L is an important growth factor in the development and homeostasis of p-preDC FC and in the role of FC inducing generation of Treg. Flt3-L provides potent immunoregulatory properties that may be clinically useful to improve tolerance induction and enhance the function of allogeneic cell therapies. Stem Cells 2018;36:1567-1577.

摘要

促进细胞(FC)是 CD8 TCR 骨髓亚群,可增强纯化造血干细胞(HSC)的植入,并在体内诱导抗原特异性 CD4 CD25 FoxP3 调节性 T 细胞(Treg)。FC 的主要亚群在表型和功能上都类似于浆细胞样前体树突状细胞(p-preDC)。在这里,我们报告 Fms 样酪氨酸激酶 3 配体敲除(Flt3-L-KO)小鼠中 FC 的数量明显减少。具体来说,B220 CD11c CD11b p-preDC FC 亚群选择性减少。Flt3-L-KO 小鼠给予 Flt3-L 后,FC 总群中的 p-preDC FC 亚群得到恢复。Flt3-L-KO 供体的 FC 表现出在同种异体 HSC 植入的促进作用受损,在同种异体骨髓移植(B6→NOD)和减强烈预处理(B6→BALB/c)的小鼠中也是如此。此外,Flt3-L-KO 小鼠的 CD4 CD25 Foxp3 Treg 数量显著减少。这与 Treg 上趋化因子受体 CXCR3 或 CCR5 的表达有关。与野生型 Treg 相比,Flt3-L-KO 小鼠脾脏中的 Treg 促进同种异体 HSC 植入的能力受损。Flt3-L 处理显著扩增了 Treg,并恢复了其促进功能。这些结果表明,Flt3-L 是 p-preDC FC 发育和稳态以及 FC 诱导 Treg 生成中重要的生长因子。Flt3-L 提供了强大的免疫调节特性,这在临床上可能有助于提高耐受性诱导和增强同种异体细胞治疗的功能。Stem Cells 2018;36:1567-1577.

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