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PMID: 7531149 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Actions of the chemotactic cytokines MCP-1, MCP-2, MCP-3, RANTES, MIP-1 alpha and MIP-1 beta on human monocytes.

European journal of immunology ·Vol. 25 ·No. 1 ·1995-01-00 ·Pages 64-8

Uguccioni M, D'Apuzzo M, Loetscher M, Dewald B, Baggiolini M

Abstract

The activities of six synthetic CC chemokines, MCP-1, MCP-2, MCP-3, RANTES, MIP-1 alpha and MIP-1 beta on human blood monocytes were studied. All CC chemokines elicited a bimodal migration response in vitro. Highest numbers of migrating cells were obtained with the monocyte chemotactic proteins (MCP) and RANTES, somewhat lower numbers with MIP-1 alpha, and only weak migration with MIP-1 beta. The most potent attractants were MCP-1 and MIP-1 alpha which reached maximum efficacy at 0.1 to 1 nM. All CC chemokines also induced the release of N-acetyl-beta-D-glucosaminidase from cytochalasin B-pretreated monocytes. The MCP were most effective (MCP-1 > MCP-3 > MCP-2), RANTES and MIP-1 alpha showed moderate (1/3 of MCP-1 activity), and MIP-1 beta only minimal activity. Cytosolic free Ca2+ changes and exocytosis were used to monitor receptor desensitization. Marked cross-desensitization was observed among MCP-1, MCP-2 and MCP-3 on the one hand, and RANTES, MIP-1 alpha and MIP-1 beta on the other, indicating receptor sharing within these two subgroups of CC chemokines. The responses to RANTES, MIP-1 alpha and MIP-1 beta were also moderately to markedly desensitized by pretreatment with MCP-1, MCP-2 or MCP-3, while the responses to the MCP were virtually unaffected by pretreatment with RANTES, MIP-1 alpha and MIP-1 beta. These results suggest that the MCP also interact with receptors recognized by RANTES, MIP-1 alpha and MIP-1 beta, but not vice versa. Binding studies were performed with radiolabeled MCP-1 or MIP-1 alpha. All MCP competed readily for labeled MCP-1 yielding a concentration-dependent sigmoidal displacement curve. Displacement with RANTES, MIP-1 alpha and MIP-1 beta was observed at higher concentrations, but was not complete. Radiolabeled MIP-1 alpha was displaced efficiently by MIP-1 alpha or MIP-1 beta, but only partially by RANTES. Of the MCP, only MC-3 completely displaced MIP-1 alpha, while only partial displacement was observed with MCP-1 and MCP-2.

MeSH Terms
Acetylglucosaminidase/metabolism Calcium/metabolism Chemokine CCL2 Chemokine CCL4 Chemokine CCL5 Chemokine CCL7 Chemokine CCL8 Chemotactic Factors/physiology Chemotaxis, Leukocyte/physiology Cytokines/physiology Exocytosis/physiology Humans In Vitro Techniques Lymphokines/physiology Macrophage Inflammatory Proteins Monocyte Chemoattractant Proteins Monocytes/physiology Monokines/physiology Protein Binding/physiology
Chemicals
CCL7 protein, human CCL8 protein, human Chemokine CCL2 Chemokine CCL4 Chemokine CCL5 Chemokine CCL7 Chemokine CCL8 Chemotactic Factors Cytokines Lymphokines Macrophage Inflammatory Proteins Monocyte Chemoattractant Proteins Monokines Acetylglucosaminidase Calcium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Uguccioni M
Theodor-Kocher Institute, University of Bern, Switzerland.
D'Apuzzo M
Loetscher M
Dewald B
Baggiolini M
Article Info
Journal
European journal of immunology
Abbr.
Eur J Immunol
ISSN
0014-2980
Published
1995-01-00
Pages
64-8
Language
English
Region
Germany
NLM ID
1273201
Subset
IM
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