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一种在肝脏中表达的新型人类CC趋化因子——肝脏与激活调节趋化因子(LARC)的分子克隆。对淋巴细胞的趋化活性及在2号染色体上的基因定位。

Molecular cloning of a novel human CC chemokine liver and activation-regulated chemokine (LARC) expressed in liver. Chemotactic activity for lymphocytes and gene localization on chromosome 2.

作者信息

Hieshima K, Imai T, Opdenakker G, Van Damme J, Kusuda J, Tei H, Sakaki Y, Takatsuki K, Miura R, Yoshie O, Nomiyama H

机构信息

Department of Biochemistry, Kumamoto University Medical School, Honjo, Kumamoto 860, Japan.

出版信息

J Biol Chem. 1997 Feb 28;272(9):5846-53. doi: 10.1074/jbc.272.9.5846.

Abstract

Partial overlapping cDNA sequences likely to encode a novel human CC chemokine were identified from the GenBank Expressed Sequence Tag data base. Using these sequences, we isolated full-length cDNA encoding a protein of 96 amino acid residues with 20-28% identity to other CC chemokines. By Northern blot, this chemokine was mainly expressed in liver among various tissues and strongly induced in several human cell lines by phorbol myristate acetate. We thus designated this chemokine as LARC from Liver and Activation-Regulated Chemokine. We mapped the LARC gene close to the chromosomal marker D2S159 at chromosome 2q33-q37 by somatic cell and radiation hybrid mappings and isolated two yeast artificial chromosome clones containing the LARC gene from this region. To prepare LARC, we subcloned the cDNA into a baculovirus vector and expressed it in insect cells. The secreted protein started at Ala-27 and was significantly chemotactic for lymphocytes. At a concentration of 1 microg/ml, it also showed a weak chemotactic activity for granulocytes. Unlike other CC chemokines, however, LARC was not chemotactic for monocytic THP-1 cells or blood monocytes. LARC tagged with secreted alkaline phosphatase-(His)6 bound specifically to lymphocytes, the binding being competed only by LARC and not by other CC or CXC chemokines. Scatchard analysis revealed a single class of receptors for LARC on lymphocytes with a Kd of 0.4 nM and 2100 sites/cell. Collectively, LARC is a novel CC chemokine, which may represent a new group of CC chemokines localized on chromosome 2.

摘要

从GenBank表达序列标签数据库中鉴定出可能编码一种新型人类CC趋化因子的部分重叠cDNA序列。利用这些序列,我们分离出了编码一个96个氨基酸残基的蛋白质的全长cDNA,该蛋白质与其他CC趋化因子有20%-28%的同源性。通过Northern印迹分析,这种趋化因子在多种组织中主要在肝脏表达,并在几种人类细胞系中被佛波酯肉豆蔻酸酯强烈诱导。因此,我们将这种趋化因子命名为LARC,即肝脏和激活调节趋化因子。我们通过体细胞和辐射杂种定位将LARC基因定位到2号染色体q33-q37区域靠近染色体标记D2S159的位置,并从该区域分离出两个包含LARC基因的酵母人工染色体克隆。为了制备LARC,我们将cDNA亚克隆到杆状病毒载体中并在昆虫细胞中表达。分泌的蛋白质从Ala-27开始,对淋巴细胞具有显著的趋化作用。在浓度为1微克/毫升时,它对粒细胞也表现出微弱的趋化活性。然而,与其他CC趋化因子不同,LARC对单核细胞THP-1细胞或血液单核细胞没有趋化作用。用分泌性碱性磷酸酶-(His)6标记的LARC特异性结合淋巴细胞,这种结合仅被LARC竞争,而不被其他CC或CXC趋化因子竞争。Scatchard分析显示淋巴细胞上LARC有一类单一的受体,解离常数为0.4 nM,每个细胞有2100个位点。总的来说,LARC是一种新型的CC趋化因子,可能代表定位在2号染色体上的一组新的CC趋化因子。

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