Johns Hopkins Asthma and Allergy Center, 5501 Hopkins Bayview Circle, Baltimore, MD 21224, United States.
J Immunol Methods. 2012 Nov 30;385(1-2):51-9. doi: 10.1016/j.jim.2012.08.006. Epub 2012 Aug 14.
Human basophils are an accessible participant of the human allergic reaction. There is natural variation in various functional endpoints and in signaling molecule expression but there has been only a limited effort to place this information in the context of mRNA expression profiles. The goal of these studies was to develop gene transcript profiles associated with IL-3 exposure for use in probing basophil phenotypes. Highly purified human basophils were cultured under several conditions and the cells subsequently analyzed by microarray analysis of gene transcript expression. Basophils were cultured with or without IL-3 for 24 h and the expression profile, relative to pre-culture, analyzed for transcripts that act in a reciprocal fashion depending on the condition. A 51-gene transcript set was identified that was composed of 34 transcripts that increased with IL-3 and decreased without IL-3 and a further 17 transcripts that did the reverse. This set of transcripts was validated on two microarray chips. The changes induced by IL-3 were stable in time, with 3 day cultures generating a signature concordant with 1 day cultures. The inverted nature of the response to ±IL-3 suggested that the normal circulating basophil is balanced between a state of high and low IL-3 exposure and thus is very sensitive to changes in IL-3. For example, the basophil could detect the early generation of IL-3 that follows IgE-mediated stimulation of basophils. When this signature tool was applied to freshly isolated basophils, it was observed that the signature was similar for the same subjects' basophil sampled weeks apart. It was also shown that the 51-gene transcript was insensitive to the method of preparing purified basophils. Finally, these studies provided an estimate for the normal in vivo exposure of circulating basophils to IL-3 or IL-3-like functionality. These studies identified an IL-3 signature to probe changes in basophils occurring in vivo.
人类嗜碱性粒细胞是人类过敏反应的一个可及的参与者。在各种功能终点和信号分子表达方面存在自然变异,但在将这些信息置于 mRNA 表达谱的背景下的努力有限。这些研究的目的是开发与 IL-3 暴露相关的基因转录谱,用于探测嗜碱性粒细胞表型。高度纯化的人类嗜碱性粒细胞在几种条件下培养,然后通过基因转录表达的微阵列分析来分析细胞。嗜碱性粒细胞在有或没有 IL-3 的情况下培养 24 小时,并相对于预培养分析以相反方式作用的条件依赖性转录物的表达谱。确定了 51 个基因转录本集,其中包含 34 个随着 IL-3 增加而减少,而没有 IL-3 则减少的转录本和另外 17 个相反的转录本。该转录本集在两个微阵列芯片上进行了验证。IL-3 诱导的变化具有时间稳定性,3 天培养物产生的特征与 1 天培养物一致。对 ±IL-3 的反应的反转性质表明,正常循环的嗜碱性粒细胞在高和低 IL-3 暴露之间处于平衡状态,因此对 IL-3 的变化非常敏感。例如,嗜碱性粒细胞可以检测到 IgE 介导的嗜碱性粒细胞刺激后早期产生的 IL-3。当将此签名工具应用于新分离的嗜碱性粒细胞时,观察到相同受试者的嗜碱性粒细胞在相隔数周的情况下采样时,该签名相似。还表明,51 个基因转录本对纯化嗜碱性粒细胞的制备方法不敏感。最后,这些研究提供了对循环嗜碱性粒细胞体内暴露于 IL-3 或类似 IL-3 功能的正常估计。这些研究确定了一个 IL-3 特征,以探测体内发生的嗜碱性粒细胞变化。