HUMAN MONOCYTE CHEMOTACTIC PROTEIN-3 (MCP-3) - MOLECULAR-CLONING OF THE CDNA AND COMPARISON WITH OTHER CHEMOKINES

被引:108
作者
OPDENAKKER, G
FROYEN, G
FITEN, P
PROOST, P
VANDAMME, J
机构
[1] Rega Institute, Laboratory of Molecular Medicine and Immunobiology, University of Leuven, B-3000 Leuven
关键词
D O I
10.1006/bbrc.1993.1251
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
When human MG-63 osteosarcoma cells are triggered with IL-1β, they produce, among various other cytokines, also monocyte chemotactic proteins (MCPs). Homogeneous MCP-1, MCP-2 and MCP-3 were found to induce production of gelatinase B and chemotaxis of monocytes. Based on the almost complete amino acid sequence of natural MCP-3, two sets of degenerated oligonucleotides were used for the amplification of MCP-3 cDNA. Total RNA from stimulated MG-63 cells was reverse transcribed and PCRs done on the mRNA:cDNA duplex. Using the PCR-product, several cDNAs were isolated from a cDNA library of IL-1-stimulated MG-63 cells. From the cDNA sequence the complete primary structure of the protein was deduced: MCP-3 shows 71% and 58% amino acid homology with MCP-1 and MCP-2, respectively. Our study establishes MCP-3 as an inflammatory cytokine that regulates macrophage functions. Because MCP-3 is often produced by tumor cell lines and regulates protease secretion by macrophages, its production might also contribute to invasion and metastasis of cancer cells. © 1993 Academic Press.
引用
收藏
页码:535 / 542
页数:8
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