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Coordinate Up‐Regulation of the β‐Chemokine Subfamily in Autoimmune Sialoadenitis of MRL/lpr Mice
Author(s) -
Mustafa,
Sharafeldin,
Diab,
Biao Huang,
Wanxue Zhu,
Frithiof,
) Klinge
Publication year - 1998
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1046/j.1365-3083.1998.00440.x
Subject(s) - chemokine , in situ hybridization , messenger rna , macrophage inflammatory protein , immunohistochemistry , ccl3 , infiltration (hvac) , peripheral blood mononuclear cell , biology , monocyte , microbiology and biotechnology , immunology , inflammation , ccl2 , gene , biochemistry , in vitro , physics , thermodynamics
Mononuclear cell (MNC) infiltration of the salivary and lacrimal glands is a major feature in Sjogren's syndrome (SS) and its animal model, murine autoimmune sialoadenitis (MAS). To investigate factors that influence selective infiltration by MNC of submandibular glands in young and adult MRL/lpr mice with MAS, expression of mRNA encoding the β‐chemokines monocyte chemoattractant protein (MCP)‐1, macrophage inflammatory protein (MIP)‐1α, MIP‐1β and regulated upon activation, normal T‐cell expressed and secreted (RANTES) was investigated by in situ hybridization. MCP‐1 protein production was also evaluated by immunohistochemistry. Young mice with MAS showed an early up‐regulation of mRNA expression for MCP‐1, MIP‐1β and RANTES, while MIP‐1α mRNA expression was not affected. Adult mice with MAS showed a further up‐regulation of mRNA expression for MCP‐1, MIP‐1β and RANTES, and a remarkably strong up‐regulation for MIP‐1α. Immunohistochemistry revealed that MCP‐1 protein production paralleled MCP‐1 mRNA expression in both young and adult mice. These observations implicate MCP‐1, MIP‐1β and RANTES as potential chemokines in induction of MAS, and MCP‐1, MIP‐1β, RANTES and prominently MIP‐1α in progression and perturbation of MAS.