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体外人单核细胞分化过程中细胞视黄酸结合蛋白(CRABP II)的调控

Regulation of cellular retinoic acid binding protein (CRABP II) during human monocyte differentiation in vitro.

作者信息

Kreutz M, Fritsche J, Andreesen R, Krause S W

机构信息

Department of Hematology and Oncology, University of Regensburg, Germany.

出版信息

Biochem Biophys Res Commun. 1998 Jul 30;248(3):830-4. doi: 10.1006/bbrc.1998.9058.

DOI:10.1006/bbrc.1998.9058
PMID:9704013
Abstract

Cellular retinoic acid binding proteins (CRABP) are low molecular weight proteins whose precise function remains unknown. They bind retinoids and may thereby modulate the intracellular steady-state concentration of retinoids. Whereas CRABP I is ubiquitously expressed, CRABP II is mainly detected in various cell types of the skin. By representative difference analysis we found that CRABP II is also strongly expressed in human monocyte-derived macrophages (MAC) but not in freshly isolated monocytes (MO). The CRABP II mRNA was gradually upregulated during differentiation from MO to MAC in the presence of 2% serum. Adherence, which is important for MO differentiation, induced CRABP II expression, but the addition of 10(-7) M retinoic acid inhibited the upregulation of CRABP II expression during MO/MAC differentiation. As MO can differentiate along the classical pathway not only to MAC but also to dendritic cells we analyzed the expression of CRABP II in MO-derived dendritic cells cultured with 10% FCS, IL-4, and GM-CSF. In contrast to MAC, MO-derived dendritic cells showed an extremely low expression of CRABP II. From these results we conclude (1) that the availability and the metabolism of retinoids may be different in MAC compared to MO and dendritic cells and (2) that this may influence differentiation and activation of those cells.

摘要

细胞视黄酸结合蛋白(CRABP)是一类低分子量蛋白质,其确切功能尚不清楚。它们能结合类视黄醇,从而可能调节细胞内类视黄醇的稳态浓度。CRABP I在全身广泛表达,而CRABP II主要在皮肤的各种细胞类型中被检测到。通过代表性差异分析,我们发现CRABP II在人单核细胞衍生的巨噬细胞(MAC)中也强烈表达,但在新鲜分离的单核细胞(MO)中不表达。在2%血清存在的情况下,从MO向MAC分化的过程中,CRABP II mRNA逐渐上调。对于MO分化很重要的黏附诱导了CRABP II的表达,但添加10^(-7) M视黄酸会抑制MO/MAC分化过程中CRABP II表达的上调。由于MO不仅可以沿着经典途径分化为MAC,还可以分化为树突状细胞,我们分析了在含有10%胎牛血清、白细胞介素-4和粒细胞-巨噬细胞集落刺激因子的培养基中培养的MO衍生树突状细胞中CRABP II的表达。与MAC相反(对比MAC),MO衍生的树突状细胞显示出极低的CRABP II表达。从这些结果我们得出结论:(1)与MO和树突状细胞相比,MAC中类视黄醇的可用性和代谢可能不同;(2)这可能会影响这些细胞的分化和激活。

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