Substance P augments fibrogenic cytokine-induced fibroblast proliferation: possible involvement of neuropeptide in tissue fibrosis

被引:49
作者
Katayama, I [1 ]
Nishioka, K [1 ]
机构
[1] TOKYO MED & DENT UNIV,SCH MED,DEPT DERMATOL,BUNKYO KU,TOKYO 113,JAPAN
关键词
systemic sclerosis; fibrosis; mast cell; histamine; cytokine;
D O I
10.1016/S0923-1811(97)00608-7
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Sodium-butyrate-pretreated and Con A-stimulated P815 mast cell line generated 3T3 fibroblast proliferating activity. This fibroblast stimulatory activity was partially abrogated by three different substance P antagonists such as spantide (NK1 antagonist), FK224 (NK1 and NK2 antagonist) or FK888 (NK1 antagonist) or anti-substance P antibody. In addition to P815 mastocytoma cell, IL3-dependent, bone marrow-derived mast cells also generated fibroblast proliferating activity which was also partially abrogated by substance P antagonists. Anti-fibrogenic cytokine antibodies also inhibited mast cell-derived fibroblast proliferating activity. Substance P or histamine augmented fibrogenic cytokine-induced fibroblast proliferation which indicates that mast cell-derived histamine or substance P play an important role in induction of tissue fibrosis in fibrosing diseases. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:201 / 206
页数:6
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