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本文引用的文献

1
Neutrophil attractant protein-1 and monocyte chemoattractant protein-1 in human serum. Effects of intravenous lipopolysaccharide on free attractants, specific IgG autoantibodies and immune complexes.人血清中的中性粒细胞趋化蛋白-1和单核细胞趋化蛋白-1。静脉注射脂多糖对游离趋化因子、特异性IgG自身抗体和免疫复合物的影响。
J Immunol. 1993 Sep 15;151(6):3292-8.
2
Interleukin-8 and related chemotactic cytokines--CXC and CC chemokines.白细胞介素-8及相关趋化细胞因子——CXC和CC趋化因子。
Adv Immunol. 1994;55:97-179.
3
Macrophage inflammatory protein 1 alpha, interleukin 3 and diffusible marrow stromal factors maintain human hematopoietic stem cells for at least eight weeks in vitro.巨噬细胞炎性蛋白1α、白细胞介素3和可扩散骨髓基质因子可使人类造血干细胞在体外维持至少8周。
J Exp Med. 1994 Feb 1;179(2):643-9. doi: 10.1084/jem.179.2.643.
4
Human hemofiltrate as a source of circulating bioactive peptides: determination of amino acids, peptides and proteins.作为循环生物活性肽来源的人血液滤过液:氨基酸、肽和蛋白质的测定
Biomed Chromatogr. 1994 Mar-Apr;8(2):90-4. doi: 10.1002/bmc.1130080209.
5
Monocyte chemotactic proteins MCP-1, MCP-2, and MCP-3 are major attractants for human CD4+ and CD8+ T lymphocytes.单核细胞趋化蛋白MCP - 1、MCP - 2和MCP - 3是人类CD4 +和CD8 + T淋巴细胞的主要趋化因子。
FASEB J. 1994 Oct;8(13):1055-60. doi: 10.1096/fasebj.8.13.7926371.
6
Distinct and overlapping direct effects of macrophage inflammatory protein-1 alpha and transforming growth factor beta on hematopoietic progenitor/stem cell growth.巨噬细胞炎性蛋白-1α和转化生长因子β对造血祖细胞/干细胞生长的不同及重叠直接作用
Blood. 1994 Oct 1;84(7):2175-81.
7
Antagonists of monocyte chemoattractant protein 1 identified by modification of functionally critical NH2-terminal residues.通过对功能关键的氨基末端残基进行修饰鉴定出的单核细胞趋化蛋白1拮抗剂。
J Exp Med. 1995 Feb 1;181(2):631-40. doi: 10.1084/jem.181.2.631.
8
Actions of the chemotactic cytokines MCP-1, MCP-2, MCP-3, RANTES, MIP-1 alpha and MIP-1 beta on human monocytes.趋化细胞因子MCP-1、MCP-2、MCP-3、RANTES、MIP-1α和MIP-1β对人单核细胞的作用。
Eur J Immunol. 1995 Jan;25(1):64-8. doi: 10.1002/eji.1830250113.
9
CD34+/CD33- cells reselected from macrophage inflammatory protein 1 alpha+interleukin-3--supplemented "stroma-noncontact" cultures are highly enriched for long-term bone marrow culture initiating cells.从巨噬细胞炎性蛋白1α+白细胞介素-3补充的“基质非接触”培养物中重新选择的CD34+/CD33-细胞高度富集了长期骨髓培养起始细胞。
Blood. 1994 Sep 1;84(5):1442-9.
10
Monocyte chemotactic protein 3 is a most effective basophil- and eosinophil-activating chemokine.单核细胞趋化蛋白3是一种最有效的嗜碱性粒细胞和嗜酸性粒细胞激活趋化因子。
J Exp Med. 1994 Feb 1;179(2):751-6. doi: 10.1084/jem.179.2.751.

HCC-1,一种源自人血浆的新型趋化因子。

HCC-1, a novel chemokine from human plasma.

作者信息

Schulz-Knappe P, Mägert H J, Dewald B, Meyer M, Cetin Y, Kubbies M, Tomeczkowski J, Kirchhoff K, Raida M, Adermann K, Kist A, Reinecke M, Sillard R, Pardigol A, Uguccioni M, Baggiolini M, Forssmann W G

机构信息

Lower Saxony Institute for Peptide Research (IPF), Hannover, Germany.

出版信息

J Exp Med. 1996 Jan 1;183(1):295-9. doi: 10.1084/jem.183.1.295.

DOI:10.1084/jem.183.1.295
PMID:8551235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2192403/
Abstract

A novel CC chemokine, HCC-1, was isolated from the hemofiltrate of patients with chronic renal failure. HCC-1 has a relative molecular mass of 8,673 and consists of 74 amino acids including four cysteines linked to disulfide bonds. HCC-1 cDNA was cloned from human bone marrow and shown to code for the mature protein plus a putative 19-residue leader sequence. Mature HCC-1 has sequence identity of 46% with macrophage inflammatory protein (MIP)-1 alpha and MIP-1 beta, and 29-37% with the other human CC chemokines. Unlike MIP-1 alpha and the other CC chemokines, HCC-1 is expressed constitutively in several normal tissues (spleen, liver, skeletal and heart muscle, gut, and bone marrow), and is present at high concentrations (1-80 nM) in plasma. HCC-1 has weak activities on human monocytes and acts via receptors that also recognize MIP-1 alpha. It induced intracellular Ca2+ changes and enzyme release, but no chemotaxis, at concentrations of 100-1,000 nM, and was inactive on T lymphocytes, neutrophils, and eosinophil leukocytes. In addition, HCC-1 enhanced the proliferation of CD34+ myeloid progenitor cells. It was as effective as MIP-1 alpha, but about 100-fold less potent.

摘要

一种新型CC趋化因子HCC-1是从慢性肾衰竭患者的血液滤过液中分离出来的。HCC-1的相对分子质量为8673,由74个氨基酸组成,其中包括通过二硫键相连的4个半胱氨酸。HCC-1 cDNA是从人骨髓中克隆出来的,编码成熟蛋白以及一个推测的含19个残基的前导序列。成熟的HCC-1与巨噬细胞炎性蛋白(MIP)-1α和MIP-1β的序列同一性为46%,与其他人CC趋化因子的序列同一性为29%-37%。与MIP-1α和其他CC趋化因子不同,HCC-1在几种正常组织(脾脏、肝脏、骨骼肌和心肌、肠道和骨髓)中组成性表达,并且在血浆中以高浓度(1-80 nM)存在。HCC-1对人单核细胞具有微弱活性,通过也能识别MIP-1α的受体发挥作用。在浓度为100-1000 nM时,它能诱导细胞内Ca2+变化和酶释放,但不引起趋化作用,对T淋巴细胞、中性粒细胞和嗜酸性粒细胞无活性。此外,HCC-1增强了CD34+髓系祖细胞的增殖。它与MIP-1α效果相当,但效力约低百倍。