Xu S, Ariizumi K, Edelbaum D, Bergstresser P R, Takashima A
Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235, USA.
Eur J Immunol. 1995 Apr;25(4):1018-24. doi: 10.1002/eji.1830250424.
We have recently established dendritic cell (DC) lines (XS series) from the epidermis of newborn mice by repeated feeding with granulocyte/macrophage-colony-stimulating factor (GM-CSF) and culture supernatants from skin-derived stromal cell lines (NS series). XS lines resemble resident Langerhans cell (LC), which are immature DC that reside in epidermis, by their surface phenotype and antigen-presenting profile. XS lines further resemble resident LC in that they express mRNA for interleukin-1 beta and macrophage inflammatory protein (MIP)-1 alpha, and by the absence of mRNA for IL-6. Their growth is promoted by GM-CSF, colony-stimulating factor-1 (CSF-1), or NS culture supernatant, and inhibited by interferon-gamma or tumor necrosis factor-alpha. The expression by the XS lines of Ia molecules is up-regulated by GM-CSF, and down-regulated by NS supernatant. These results suggest the existence of negative regulatory mechanisms in which the growth and/or maturation of DC is suppressed by selected cytokines.
我们最近通过用粒细胞/巨噬细胞集落刺激因子(GM-CSF)和皮肤来源的基质细胞系(NS系列)的培养上清液反复培养,从新生小鼠的表皮建立了树突状细胞(DC)系(XS系列)。XS系通过其表面表型和抗原呈递特征,类似于驻留的朗格汉斯细胞(LC),后者是驻留在表皮中的未成熟DC。XS系在表达白细胞介素-1β和巨噬细胞炎性蛋白(MIP)-1α的mRNA以及不表达IL-6的mRNA方面,进一步类似于驻留的LC。GM-CSF、集落刺激因子-1(CSF-1)或NS培养上清液可促进它们的生长,而干扰素-γ或肿瘤坏死因子-α则抑制其生长。GM-CSF可上调XS系Ia分子的表达,而NS上清液则使其下调。这些结果表明存在负调控机制,其中特定细胞因子可抑制DC的生长和/或成熟。