PMID- 8301133 OWN - NLM STAT- MEDLINE DCOM- 19940309 LR - 20220318 IS - 0022-1767 (Print) IS - 0022-1767 (Linking) VI - 152 IP - 3 DP - 1994 Feb 1 TI - Macrophage inflammatory protein-1 alpha and monocyte chemoattractant peptide-1 elicit immediate and late cutaneous reactions and activate murine mast cells in vivo. PG - 1298-303 AB - We have previously reported that monocyte chemoattractant protein-1 (MCP-1) is the most potent histamine-releasing factor (HRF) for basophils. Macrophage inflammatory protein-1 alpha (MIP-1 alpha) has modest histamine-releasing activity. The objective of this study was to investigate whether MCP-1 and MIP-1 alpha would activate mast cells in vivo and induce a cutaneous inflammatory reaction in mice. To this goal, mouse hind footpads were separately injected with 20 microliters of human recombinant MCP-1 or MIP-1 alpha (10(-7) M). Diluent was used as a control in the second footpad. The footpad-swelling response was measured at 30 min, 1 h, and then hourly for 6 h. Both MCP-1 (2.72 +/- 0.2 vs 2.1 +/- 0.03 mm for diluent, n = 8, p < 0.02) and MIP-1 alpha (3.0 +/- 0.1 vs 2.1 +/- 0.03 mm for diluent, n = 8, p < 0.02) induced an immediate swelling reaction. The immediate reaction was followed by a sustained late reaction that peaked within 1 h and lasted for more than 6 h. Histologic examination of the footpads, obtained at hour 2, revealed that MCP-1 caused mild mononuclear cell infiltrates, moderate degranulation of mast cells, and soft tissue swelling. In contrast, MIP-1 alpha induced a severe inflammatory reaction that consisted of neutrophils, mononuclear cells, and degranulated mast cells. Electron microscope examination of the tissue revealed features of extensive mast cell degranulation by MIP-1 alpha and to a lesser extent by MCP-1. Thus, we conclude that mast cells are activated on injection of MCP-1, whereas degranulation of mast cells and recruitment of leukocytes contribute to the footpad reaction induced with MIP-1 alpha. FAU - Alam, R AU - Alam R AD - Department of Internal Medicine, University of Texas Medical Branch, Galveston 77555-0762. FAU - Kumar, D AU - Kumar D FAU - Anderson-Walters, D AU - Anderson-Walters D FAU - Forsythe, P A AU - Forsythe PA LA - eng GR - A12294/PHS HHS/United States GR - A127864/PHS HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Immunol JT - Journal of immunology (Baltimore, Md. : 1950) JID - 2985117R RN - 0 (Chemokine CCL2) RN - 0 (Chemokine CCL4) RN - 0 (Chemotactic Factors) RN - 0 (Cytokines) RN - 0 (Macrophage Inflammatory Proteins) RN - 0 (Monokines) SB - IM MH - Animals MH - Cell Degranulation MH - Chemokine CCL2 MH - Chemokine CCL4 MH - Chemotactic Factors/*immunology MH - Chemotaxis, Leukocyte MH - Cytokines/*immunology MH - Immunity, Cellular MH - Macrophage Inflammatory Proteins MH - Mast Cells/*immunology MH - Mice MH - Mice, Inbred BALB C MH - Microscopy, Electron MH - Monokines/*immunology MH - Skin Tests EDAT- 1994/02/01 00:00 MHDA- 1994/02/01 00:01 CRDT- 1994/02/01 00:00 PHST- 1994/02/01 00:00 [pubmed] PHST- 1994/02/01 00:01 [medline] PHST- 1994/02/01 00:00 [entrez] PST - ppublish SO - J Immunol. 1994 Feb 1;152(3):1298-303.