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单核细胞表面糖胺聚糖正向调节白细胞介素-4诱导的向树突状细胞的分化。

Monocyte cell surface glycosaminoglycans positively modulate IL-4-induced differentiation toward dendritic cells.

作者信息

den Dekker Els, Grefte Sander, Huijs Tonnie, ten Dam Gerdy B, Versteeg Elly M M, van den Berk Lieke C J, Bladergroen Bellinda A, van Kuppevelt Toin H, Figdor Carl G, Torensma Ruurd

机构信息

Department of Tumor Immunology, Nijmegen Centre for Molecular Life Sciences, Nijmegen, The Netherlands.

出版信息

J Immunol. 2008 Mar 15;180(6):3680-8. doi: 10.4049/jimmunol.180.6.3680.

Abstract

IL-4 induces the differentiation of monocytes toward dendritic cells (DCs). The activity of many cytokines is modulated by glycosaminoglycans (GAGs). In this study, we explored the effect of GAGs on the IL-4-induced differentiation of monocytes toward DCs. IL-4 dose-dependently up-regulated the expression of DC-specific ICAM-3-grabbing nonintegrin (DC-SIGN), CD80, CD206, and CD1a. Monocytes stained positive with Abs against heparan sulfate (HS) and chondroitin sulfate (CS) B (CSB; dermatan sulfate), but not with Abs that recognize CSA, CSC, and CSE. Inhibition of sulfation of monocyte/DC cell surface GAGs by sodium chlorate reduced the reactivity of sulfate-recognizing single-chain Abs. This correlated with hampered IL-4-induced DC differentiation as evidenced by lower expression of DC-SIGN and CD1a and a decreased DC-induced PBL proliferation, suggesting that sulfated monocyte cell surface GAGs support IL-4 activity. Furthermore, removal of cell surface chondroitin sulfates by chondroitinase ABC strongly impaired IL-4-induced STAT6 phosphorylation, whereas removal of HS by heparinase III had only a weak inhibitory effect. IL-4 bound to heparin and CSB, but not to HS, CSA, CSC, CSD, and CSE. Binding of IL-4 required iduronic acid, an N-sulfate group (heparin) and specific O sulfates (CSB and heparin). Together, these data demonstrate that monocyte cell surface chondroitin sulfates play an important role in the IL-4-driven differentiation of monocytes into DCs.

摘要

白细胞介素-4(IL-4)可诱导单核细胞向树突状细胞(DC)分化。许多细胞因子的活性受糖胺聚糖(GAG)调节。在本研究中,我们探讨了GAG对IL-4诱导单核细胞向DC分化的影响。IL-4呈剂量依赖性地上调DC特异性细胞间黏附分子-3抓取非整合素(DC-SIGN)、CD80、CD206和CD1a的表达。单核细胞对硫酸乙酰肝素(HS)和硫酸软骨素(CS)B(CSB;硫酸皮肤素)抗体染色呈阳性,但对识别CSA、CSC和CSE的抗体染色呈阴性。氯酸钠对单核细胞/DC细胞表面GAG硫酸化的抑制降低了硫酸识别单链抗体的反应性。这与IL-4诱导的DC分化受阻相关,表现为DC-SIGN和CD1a表达降低以及DC诱导的外周血淋巴细胞(PBL)增殖减少,提示硫酸化的单核细胞表面GAG支持IL-4活性。此外,用软骨素酶ABC去除细胞表面硫酸软骨素会强烈损害IL-4诱导的信号转导和转录激活因子6(STAT6)磷酸化,而用肝素酶III去除HS仅有微弱的抑制作用。IL-4与肝素和CSB结合,但不与HS、CSA、CSC、CSD和CSE结合。IL-4的结合需要艾杜糖醛酸、N-硫酸基团(肝素)和特定的O-硫酸盐(CSB和肝素)。总之,这些数据表明单核细胞表面硫酸软骨素在IL-4驱动的单核细胞向DC分化中起重要作用。

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