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Involvement of glial cell line‐derived neurotrophic factor in activation processes of rodent macrophages
Author(s) -
Hashimoto Manabu,
Nitta Atsumi,
Fukumitsu Hidefumi,
Nomoto Hiroshi,
Shen Liya,
Furukawa Shoei
Publication year - 2005
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.20368
Subject(s) - glial cell line derived neurotrophic factor , neurotrophic factors , gdnf family of ligands , microglia , microbiology and biotechnology , chemokine , biology , monocyte , tumor necrosis factor alpha , autocrine signalling , cell culture , inflammation , chemistry , immunology , receptor , biochemistry , genetics
The physiological roles of glial cell line‐derived neurotrophic factor (GDNF) expressed in the microglia/macrophages of the injured spinal cord have not yet been clarified. mRNA expression of chemokines, including monocyte chemoattractant protein (MCP)‐1, was evoked within 1 hr after transection of the spinal cord, and GDNF mRNA expression was similarly up‐regulated. Immunohistochemical analysis showed that GDNF was coexpressed with MCP‐1 in the CD11b‐positive cells. Therefore, we examined further the effects of GDNF on cultured rat peritoneal macrophages. GDNF enhanced the phagocytic activity of the macrophages via GFRα‐1, glycosylphosphatidylinositol‐anchored specific binding site of GDNF, in a c‐Ret‐independent manner. The influence of autocrine and/or paracrine GDNF synthesis was evaluated by performing activation experiments using macrophages cultured from heterozygous (+/−) GDNF gene‐deficient mice or wild‐type (+/+) mice. There were no morphological differences dependent on genetic types or stimulators. However, the GDNF mRNA level, but not the MCP‐1 or GFRα‐1 mRNA level, was substantially lower in the mutant macrophages than in the +/+ cells irrespective of stimulation with MCP‐1 or lipopolysaccharide (LPS). The phagocytic activity enhanced by MCP‐1 or LPS was significantly lower in the mutant cells (+/−) than in the +/+ ones, demonstrating the involvement of endogenous GDNF in the activation processes of macrophages in vitro and suggesting that not only neuroprotective function but also activation of macrophages is effected by the GDNF produced after a spinal cord injury. © 2005 Wiley‐Liss, Inc.