Characterization of Bone Marrow-Derived Dendritic Cells Developed in Serum-Free Media and their Ability to Prevent Type 1 Diabetes in Nonobese Diabetic Mice

Benjamin M. Looney, Anna V. Chernatynskaya, M. Clare-Salzler, C. Xia
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引用次数: 5

Abstract

Dendritic cells (DC) have been investigated as a cell-based therapy for Type 1 Diabetes (T1D). BM-DC expanded ex vivo with GM-CSF and IL-4 is typically cultured with fetal bovine serum (FBS). The effect of FBS on NOD BM-DC has not been extensively studied. In the present study we compare BM-DC generated in serum-free culture media (X-VIVO20; FBS−) with BM-DC generated in media containing 10% FBS (RPMI1640/10%FBS; FBS+). We show that FBS− BM-DC display a phenotype and cytokine-producing profile distinct from FBS+ BMDC. Additionally, compared to FBS+ BM-DC, we show evidence of an altered Th cell response induced by FBS− BM-DC. Finally, we demonstrate that only FBS− BM-DC prevent the onset of T1D and induce increased levels of CD4+Foxp3+ regulatory T cells as well as a long-lasting β cell-specific T cell response. This study indicates that serum-free media generates a more tolerogenic BM-DC capable of preventing T1D in the NOD mice.
无血清培养基中培养的骨髓来源树突状细胞的特性及其在非肥胖糖尿病小鼠中预防1型糖尿病的能力
树突状细胞(DC)作为一种基于细胞的治疗1型糖尿病(T1D)的方法已被研究。用GM-CSF和IL-4体外扩增的BM-DC通常与胎牛血清(FBS)一起培养。FBS对NOD BM-DC的影响尚未得到广泛研究。在本研究中,我们比较了无血清培养基(X-VIVO20;FBS−),在含有10%FBS的培养基中生成BM-DC (RPMI1640/10%FBS;的边后卫+)。我们发现FBS - BM-DC表现出与FBS+ BMDC不同的表型和细胞因子产生谱。此外,与FBS+ BM-DC相比,我们发现FBS - BM-DC诱导的Th细胞反应发生了改变。最后,我们证明了只有FBS - BM-DC可以预防T1D的发生,并诱导CD4+Foxp3+调节性T细胞水平的增加,以及持久的β细胞特异性T细胞反应。本研究表明,无血清培养基可在NOD小鼠中产生耐受性更强的BM-DC,能够预防T1D。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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