IL-4 enhances proliferation and mediator release in mature human mast cells

被引:186
作者
Bischoff, SC [1 ]
Sellge, G
Lorentz, A
Sebald, W
Raab, R
Manns, MP
机构
[1] Hannover Med Sch, Dept Gastroenterol & Hepatol, D-30623 Hannover, Germany
[2] Hannover Med Sch, Dept Abdominal & Transplant Surg, D-30623 Hannover, Germany
[3] Univ Wurzburg, Theodor Boveri Inst Biomed Sci, D-97074 Wurzburg, Germany
关键词
D O I
10.1073/pnas.96.14.8080
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tissue mast cells (MC) are recognized as key effector cells of immediate-type allergic reactions releasing inflammatory mediators and cytokines on stimulation with antigen, but they also might be involved in IgE-independent inflammatory and tissue repair processes. The mechanism of human MC regulation in tissue is not fully understood. Here, we show that IL-4. in synergy with stem cell factor (SCF), regulates the function of purified human MC isolated from intestinal tissue. Whereas SCF induced only marginal proliferation of MC cultured in vitro up to 4 weeks, addition of IL-4 and SCF strongly increased the proliferation rate. Moreover, IL-4, which by itself had no visible effect on human MC, enhanced the release of histamine, leukotriene C-4, and IL-5 in MC triggered by IgE receptor crosslinking. The IL-4 effects occurred In a dose-dependent fashion (ED50 = 100 pg/ml) and could be totally blocked by a competitive IL-4 receptor antagonist. Our data indicate that IL-4 is an important regulator of human MC function and suggest that mature MC retain the capacity to proliferate in a particular tissue environment.
引用
收藏
页码:8080 / 8085
页数:6
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