Liao T N, Hsieh K H
Department of Pediatrics, National Taiwan University College of Medicine, Taipei, Republic of China.
J Clin Immunol. 1992 Jul;12(4):248-58. doi: 10.1007/BF00918148.
Histamine-releasing factors (HRFs) are a group of cytokines that cause histamine release (HR) from basophils and mast cells. The concept of the priming effect of cytokines and the heterogeneity of IgE involved in the HRF-induced HR have been emphasized in recent years. In this study, we performed a series of experiments to elucidate the above-mentioned hypotheses. The stock HRF were obtained by stimulating mononuclear cells (MNC) with phytohemagglutinin (PHA). Maximal activity was observed 36 hr after culture. By gel filtration, HRF was eluted with a peak activity ranging from 12 to 18 KD. A large portion (75%) of HRF activity could be neutralized by a combination of antibodies against interleukin 1 (IL-1), IL-3, IL-8, granulocyte-macrophage colony-stimulating factor (GM-CSF), and tumor necrosis factor-alpha (TNF-alpha). The stimulation of basophils with 100 ng/ml each of IL-3, IL-6, IL-7, GM-CSF, or TNF-alpha alone caused 10% HR; however, when the cells were pretreated with 10 ng/ml of either IL-3, IL-6, IL-7, IL-8, TNF-alpha, or GM-CSF and then stimulated with anti-IgE, a marked increase in HR was regularly observed. The combination of 100 ng/ml each of IL-1, IL-3, IL-8, GM-CSF, and TNF-alpha could induce only about 20% HR; furthermore, such combinations did not have an additive or synergistic priming effect on anti-IgE-induced HR compared to the effect of single cytokines. Stripping of surface-bound IgE with lactic acid markedly reduced the capacity of basophils to release histamine in response to MNC-HRF and anti-IgE. Passive sensitization of IgE-stripped basophils with high-HRF responders' serum could restore their responsiveness to both MNC-HRF and anti-IgE, but passive sensitization with low-HRF responders' serum could restore responsiveness to anti-IgE only. Moreover, passage of MNC-HRF through high-, but not low-HRF, responders' IgE-Sepharose columns significantly reduced the HR activity of MNC-HRF. Finally, although the eluant could induce only 10% HR, the majority of its HR activity could be restored by the addition of effluent but not by the mixture of IL-1, IL-3, IL-8, GM-CSF, and TNF-alpha, suggesting the presence of a complex interaction among those cytokines. In summary, MNC-HRF contained at least two types of HRF activity; one was IgE dependent and the other was IgE independent.(ABSTRACT TRUNCATED AT 400 WORDS)
组胺释放因子(HRFs)是一类可导致嗜碱性粒细胞和肥大细胞释放组胺(HR)的细胞因子。近年来,细胞因子的启动效应概念以及HRF诱导的HR中涉及的IgE异质性受到了重视。在本研究中,我们进行了一系列实验以阐明上述假说。储备的HRF是通过用植物血凝素(PHA)刺激单核细胞(MNC)获得的。培养36小时后观察到最大活性。通过凝胶过滤,HRF在12至18KD的峰活性处被洗脱。抗白细胞介素1(IL-1)、IL-3、IL-8、粒细胞-巨噬细胞集落刺激因子(GM-CSF)和肿瘤坏死因子-α(TNF-α)的抗体组合可中和大部分(75%)的HRF活性。单独用100ng/ml的IL-3、IL-6、IL-7、GM-CSF或TNF-α刺激嗜碱性粒细胞可导致10%的HR;然而,当细胞先用10ng/ml的IL-3、IL-6、IL-7、IL-8、TNF-α或GM-CSF预处理,然后用抗IgE刺激时,经常观察到HR显著增加。100ng/ml的IL-1、IL-3、IL-8、GM-CSF和TNF-α的组合仅能诱导约20%的HR;此外,与单一细胞因子的作用相比,这种组合对抗IgE诱导的HR没有相加或协同的启动效应。用乳酸去除表面结合的IgE可显著降低嗜碱性粒细胞对MNC-HRF和抗IgE释放组胺的能力。用高HRF反应者的血清对IgE去除的嗜碱性粒细胞进行被动致敏可恢复其对MNC-HRF和抗IgE的反应性,但用低HRF反应者的血清进行被动致敏仅能恢复对抗IgE的反应性。此外,MNC-HRF通过高HRF反应者而非低HRF反应者的IgE-琼脂糖柱后,其HR活性显著降低。最后,尽管洗脱液仅能诱导10%的HR,但其大部分HR活性可通过添加流出液恢复,而不能通过IL-1、IL-3、IL-8、GM-CSF和TNF-α的混合物恢复,这表明这些细胞因子之间存在复杂的相互作用。总之,MNC-HRF至少包含两种类型的HRF活性;一种是IgE依赖性的,另一种是IgE非依赖性的。(摘要截短至400字)