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
Lower Saxony Institute for Peptide Research (IPF), Hannover, Germany.
J Exp Med. 1996 Jan 1;183(1):295-9. doi: 10.1084/jem.183.1.295.
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.
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。