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In vivo properties of monocyte chemoattractant protein‐1
Author(s) -
Gu Long,
Rutledge Barbara,
Fiorillo Joseph,
Ernst Catherine,
Grewal Iqbal,
Flavell Richard,
Gladue Ron,
Rollins Barrett
Publication year - 1997
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1002/jlb.62.5.577
Subject(s) - monocyte , biology , in vivo , immunology , ccl2 , infiltration (hvac) , chemokine , inflammation , physics , microbiology and biotechnology , thermodynamics
Monocyte chemoattractant protein‐1 (MCP‐1) attracts monocytes, memory T lymphocytes, and natural killer (NK) cells in vitro. Its expression has been documented in disorders characterized by mononuclear cell infiltrates, suggesting that it may contribute to the inflammatory component of such diseases as atherosclerosis, multiple sclerosis, or rheumatoid arthritis. To prove a causal association, the in vivo properties of MCP‐1 must be understood. Several lines of transgenic mice have been constructed to address this question. A transgenic line in which MCP‐1 expression is controlled by the MMTV‐LTR expressed high levels of MCP‐1 in multiple organs but showed no evidence for monocyte infiltration. Instead, these mice were more susceptible to infection by the intracellular pathogens, Listeria monocytogenes and Mycobacterium tuberculosis. These mice had high serum levels of MCP‐1, suggesting that their circulating monocytes may have been desensitized or that MCP‐1 stimulated a Th2‐dominant response. In contrast, another model in which MCP‐1 expression was controlled by the insulin promoter demonstrated a monocytic infiltrate in pancreatic islets. These results indicate that MCP‐1 expression at low levels in an anatomically confined area results in monocyte infiltration, suggesting that when properly expressed, MCP‐1's in vitro properties are reproduced in vivo. This justifies the examination of MCP‐1‐deficient mice in disease models in order to explore MCP‐1's role in pathogenesis. J. Leukoc. Biol. 62: 577–580; 1997.