Obata T, Nagakura T, Kanbe M, Masaki T, Maekawa K, Yamashita K
Division of Molecular Cell Biology, Jikei University School of Medicine, Tokyo, Japan.
Biochem Biophys Res Commun. 1996 Aug 23;225(3):1015-20. doi: 10.1006/bbrc.1996.1287.
To elucidate the characterization of cultured human mast cells, the generation of prostaglandin D2 (PGD2) upon stimulation with IgE-anti IgE challenge was determined by using gas chromatography/mass spectrometry/selected ion monitoring (GC/MS/SIM) assay. Mononuclear cells obtained from human umbilical cord blood were cultured in the presence of Steel Factor, IL-6, and PGE2. After 8 weeks of culture, approximately 90 to 95% of cultured cells became tryptase-positive and included basophilic granules. At 12 weeks of culture, cells were harvested and incubated with 1 microgram/ml of human IgE for 1 hr and then challenged with 10 micrograms/ml of anti-IgE. The level of PGD2 release into the supernatant was measured by GC/MS/SIM with the stable isotope dilution method. Cyclooxygenase inhibitors affected the PGD2 release from the cell by IgE-anti IgE challenge incubation. Indomethacin inhibited 98% of PGD2 release. Acetylsalicylic acid (aspirin) and NS-398 (potent COX-2 inhibitor) also inhibited PGD2 release by 85 and 45% respectively.
为阐明培养的人肥大细胞的特性,通过气相色谱/质谱/选择离子监测(GC/MS/SIM)分析法,测定了用IgE-抗IgE激发刺激后前列腺素D2(PGD2)的生成情况。从人脐带血中获得的单核细胞在Steel因子、白细胞介素-6和前列腺素E2存在的情况下进行培养。培养8周后,约90%至95%的培养细胞变为类胰蛋白酶阳性,并含有嗜碱性颗粒。培养12周时,收获细胞,用1微克/毫升的人IgE孵育1小时,然后用10微克/毫升的抗IgE进行激发。采用稳定同位素稀释法,通过GC/MS/SIM测定上清液中PGD2的释放水平。环氧化酶抑制剂通过IgE-抗IgE激发孵育影响细胞中PGD2的释放。吲哚美辛抑制了98%的PGD2释放。乙酰水杨酸(阿司匹林)和NS-398(强效COX-2抑制剂)也分别抑制了85%和45%的PGD2释放。