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一种新型趋化因子,巨噬细胞炎症蛋白相关蛋白-2,可抑制骨髓髓系祖细胞的集落形成。

A novel chemokine, macrophage inflammatory protein-related protein-2, inhibits colony formation of bone marrow myeloid progenitors.

作者信息

Youn B S, Jang I K, Broxmeyer H E, Cooper S, Jenkins N A, Gilbert D J, Copeland N G, Elick T A, Fraser M J, Kwon B S

机构信息

Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis 46202, USA.

出版信息

J Immunol. 1995 Sep 1;155(5):2661-7.

PMID:7650394
Abstract

A new member of the beta-chemokine family, macrophage inflammatory protein (MIP)-related protein-2 (MRP-2) was isolated from a murine macrophage cell line, RAW 264.7. MRP-2 is composed of 122 amino acids of which the first 21 residues constitute a putative signal sequence. The putative mature protein is composed of 101 amino acids with a molecular weight of 11,600. MRP-2 is structurally similar to MIP-related protein-1 (MRP-1) (C10) and MIP-1 alpha. MRP-2 shows a 50.8% sequence identity at the protein level to MRP-1 and 46.3% identity to MIP-1 alpha. MRP-2 detects approximately 1.3 kilobase mRNA from monocyte and macrophage cell lines but does not detect the mRNA from T and B cells. The MRP-2 gene termed Scya9 was mapped to the central region of mouse chromosome 11 near the Scya1 and Scya2 genes, which are also members of the beta-chemokine superfamily. The Scya gene cluster was located between neurofibromatosis type 1 (Nf1) and myeloperoxidase (Mpo). rMRP-2 significantly suppressed colony formation by murine and human bone marrow granulocyte-macrophage (CFU-granulocyte-macrophage), erythroid (burst-forming unit-E), and multipotential (CFU-granulocyte-erythroid-macrophage-megakaryocyte) progenitor cells stimulated by combinations of growth factors.

摘要

从鼠巨噬细胞系RAW 264.7中分离出β-趋化因子家族的一个新成员,巨噬细胞炎性蛋白(MIP)相关蛋白-2(MRP-2)。MRP-2由122个氨基酸组成,其中前21个残基构成一个假定的信号序列。假定的成熟蛋白由101个氨基酸组成,分子量为11,600。MRP-2在结构上与MIP相关蛋白-1(MRP-1)(C10)和MIP-1α相似。MRP-2在蛋白质水平上与MRP-1的序列同一性为50.8%,与MIP-1α的同一性为46.3%。MRP-2可检测到单核细胞和巨噬细胞系中约1.3千碱基的mRNA,但未检测到T细胞和B细胞中的mRNA。被称为Scya9的MRP-2基因被定位到小鼠染色体11的中央区域,靠近Scya1和Scya2基因,它们也是β-趋化因子超家族的成员。Scya基因簇位于1型神经纤维瘤病(Nf1)和髓过氧化物酶(Mpo)之间。重组MRP-2显著抑制了由生长因子组合刺激的鼠和人骨髓粒细胞-巨噬细胞(CFU-粒细胞-巨噬细胞)、红系(爆式形成单位-E)和多能(CFU-粒细胞-红系-巨噬细胞-巨核细胞)祖细胞的集落形成。

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