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内皮分化间充质基质细胞的免疫调节:对T细胞和自然杀伤细胞的影响。

Immunomodulation of endothelial differentiated mesenchymal stromal cells: impact on T and NK cells.

作者信息

El Omar Reine, Xiong Yu, Dostert Gabriel, Louis Huguette, Gentils Monique, Menu Patrick, Stoltz Jean-François, Velot Émilie, Decot Véronique

机构信息

Université de Lorraine, UMR CNRS 7365, Ingénierie moléculaire et physiopathologie articulaire (IMoPa), Batiment Biopole, Faculté de Médecine, Vandoeuvre-Les-Nancy, France.

Fédération de Recherche 3209, CNRS-INSERM-Université de Lorraine-CHU, Nancy, France.

出版信息

Immunol Cell Biol. 2016 Apr;94(4):342-56. doi: 10.1038/icb.2015.94. Epub 2015 Oct 29.

Abstract

Wharton's jelly mesenchymal stromal cells (WJ-MSCs) are promising candidates for tissue engineering, as their immunomodulatory activity allows them to escape immune recognition and to suppress several immune cell functions. To date, however, few studies have investigated the effect of differentiation of the MSCs on this immunomodulation. To address this question, we sought to determine the impact of differentiation toward endothelial cells on immunoregulation by WJ-MSCs. Following differentiation, the endothelial-like cells (ELCs) were positive for CD31, vascular endothelial cadherin and vascular endothelial growth factor receptor 2, and able to take up acetylated low-density lipoproteins. The expression of HLA-DR and CD86, which contribute to MSCs immunoprivilege, was still weak after differentiation. We then co-cultured un- and differentiated MSCs with immune cells, under conditions of both direct and indirect contact. The proliferation and phenotype of the immune cells were analyzed and the mediators secreted by both ELCs and WJ-MSCs quantified. Interleukin (IL)-6, IL-1β, prostaglandin E2 and in particular indoleamine-2,3-dioxygenase expression were upregulated in ELCs on stimulation by T and NK cells, suggesting the possible involvement of these factors in allosuppression. ELCs co-cultured with T cells were able to generate CD25(+) T cells, which were shown to be of the CD4(+)CD25(+)FoxP3(+) regulatory subset. Direct contact between NK cells and ELCs or WJ-MSCs decreased the level of NK-activating receptor natural-killer group 2, member D. Moreover, direct co-culturing with ELCs stimulates CD73 acquisition on NK cells, a mechanism which may induce adenosine secretion by the cells and lead to an immunosuppressive function. Taken together, our results show that ELCs obtained following differentiation of WJ-MSCs remain largely immunosuppressive.

摘要

华通氏胶间充质基质细胞(WJ-MSCs)是组织工程领域颇具潜力的细胞,因其免疫调节活性使其能够逃避免疫识别并抑制多种免疫细胞功能。然而,迄今为止,很少有研究探讨间充质干细胞分化对这种免疫调节的影响。为解决这一问题,我们试图确定WJ-MSCs向内皮细胞分化对免疫调节的影响。分化后,内皮样细胞(ELCs)CD31、血管内皮钙黏蛋白和血管内皮生长因子受体2呈阳性,且能够摄取乙酰化低密度脂蛋白。分化后,对间充质干细胞免疫豁免起作用的HLA-DR和CD86表达仍然较弱。然后,我们将未分化和已分化的间充质干细胞与免疫细胞在直接和间接接触条件下共培养。分析免疫细胞的增殖和表型,并对ELCs和WJ-MSCs分泌的介质进行定量。T细胞和NK细胞刺激后,ELCs中白细胞介素(IL)-6、IL-1β、前列腺素E2,特别是吲哚胺-2,3-双加氧酶表达上调,提示这些因子可能参与同种异体抑制。与T细胞共培养的ELCs能够产生CD25(+) T细胞,结果表明这些细胞属于CD4(+)CD25(+)FoxP3(+)调节亚群。NK细胞与ELCs或WJ-MSCs直接接触会降低NK激活受体自然杀伤细胞组2成员D的水平。此外,与ELCs直接共培养会刺激NK细胞获得CD73,这一机制可能诱导细胞分泌腺苷并导致免疫抑制功能。综上所述,我们的结果表明,WJ-MSCs分化后获得的ELCs在很大程度上仍具有免疫抑制作用。

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