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巨噬细胞移动抑制因子(MIF)对MHC-II、共刺激、黏附、受体及细胞因子分子表达的体外和体内调节

In vitro and in vivo regulation by macrophage migration inhibitory factor (MIF) of expression of MHC-II, costimulatory, adhesion, receptor, and cytokine molecules.

作者信息

Stavitsky Abram B, Xianli Jia

机构信息

Department of Molecular Biology and Microbiology, Case Western Reserve University, Cleveland, OH 44120, USA.

出版信息

Cell Immunol. 2002 May-Jun;217(1-2):95-104. doi: 10.1016/s0008-8749(02)00516-6.

Abstract

The secretion of macrophage migration inhibitory factor (MIF) is enhanced by inflammatory and other stimuli. MIF regulates innate and adaptive immune responses, but the mechanisms of this regulation are poorly understood. Our hypothesis was that MIF generated by these stimuli regulates these responses by modulating key molecular expression. This hypothesis was tested by adding greater than constitutive concentrations of recombinant MIF to cultures of various cell types and flow cytometric assay. MIF modulated surface expression of MHC-II, B7-2, CD40, CD40 ligand, ICAM-1 and Fcgamma, CR1/CR2, and IL-10 receptors and intracellular expression of IL-10, TNFalpha, and p40 (IL-12). MIF increased expression of B7-1 by B cells and CD40 L by T cells in spleens from Schistosoma mansoni-infected mice. Footpad injection of MIF reduced expression of MHC-II and CD40 by B cells in draining lymph nodes. Footpad injection of Mab to MIF reduced expression of B7-2 and CR1/CR2 by B cells and B7-2 by macrophages in these nodes. These data support our hypothesis.

摘要

巨噬细胞移动抑制因子(MIF)的分泌会因炎症及其他刺激而增强。MIF可调节先天性和适应性免疫反应,但其调节机制尚不清楚。我们的假设是,这些刺激产生的MIF通过调节关键分子的表达来调控这些反应。通过向各种细胞类型的培养物中添加高于组成浓度的重组MIF并进行流式细胞术分析来验证这一假设。MIF调节MHC-II、B7-2、CD40、CD40配体、ICAM-1和Fcγ、CR1/CR2以及IL-10受体的表面表达,以及IL-10、TNFα和p40(IL-12)的细胞内表达。MIF增加了曼氏血吸虫感染小鼠脾脏中B细胞的B7-1表达和T细胞的CD40L表达。足垫注射MIF可降低引流淋巴结中B细胞的MHC-II和CD40表达。足垫注射抗MIF单克隆抗体可降低这些淋巴结中B细胞的B7-2和CR1/CR2表达以及巨噬细胞的B7-2表达。这些数据支持了我们的假设。

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