Inhibitory effect of retinoic acid on proliferation, maturation and tryptase level in human leukemic mast cells (HMC-1)

被引:23
作者
Alexandrakis, MG
Kyriakou, DS
Seretakis, D
Boucher, W
Letourneau, R
Kempuraj, D
Theoharides, TC [1 ]
机构
[1] Univ Crete, Univ Hosp Heraklion, Sch Med, Dept Hematol, Iraklion, Crete, Greece
[2] Tufts Univ, Sch Med, Dept Pharmacol & Expt Therapeut, Boston, MA 02111 USA
[3] Tufts Univ New England Med Ctr, Boston, MA 02111 USA
关键词
HMC-1; retinoic acid; tryptase; mast cells;
D O I
10.1177/039463200301600106
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mast cells play an important role in allergic inflammation by releasing histamine, tryptase and several inflammatory cytokines. Human leukemic mast cells (HMC-1) have been used to study mast cell mediators and their role in inflammatory mechanisms. HMC-1 contain and release several inflammatory mediators, of which the proteolytic enzyme tryptase is most characteristic. Retinoids, including retinoic acid, are naturally occurring and synthetic derivatives of vitamin A. All-trans-retinoic (ATRA) acid had been previously reported to inhibit cell proliferation, differentiation and apoptosis. In the present study, we investigated the effect of ATRA on the proliferation and secretion of tryptase in HMC-1. HMC-1 were treated with ATRA at 10(-4)M, 10(-5)M or 10(-6)M for 3, 4 or 5 days in culture. Control HMC- 1 were treated with equal amount of culture medium only. ATRA decreased the number of HMC-1 as compared to the control group. The same treatment for 3, 4 or 5 days also decreased intracellular tryptase levels. These results indicate that ATRA significantly inhibits both proliferation and growth as shown by the decreased intracellular tryptase levels in HMC-1. ATRA may be a useful agent in the treatment of mast cell proliferative disorders.
引用
收藏
页码:43 / 47
页数:5
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