Lería Francisca, Marco Roberto, Medina Francisco Javier
Centro de Investigaciones Biológicas (CSIC), E-28040 Madrid, Spain.
Microsc Res Tech. 2004 Sep;65(1-2):86-100. doi: 10.1002/jemt.20109.
We explored the use of microwave technology in fixation with the objective of achieving quicker fixation regimes, lower concentrations of toxic and volatile reagents, and enhanced antigen detection. We used a modified domestic microwave oven (900 W) and a low-power (5 W) microwave bench. The work was done on plant materials. The oven was supplemented with a cooling device, a stirring system, and a record of the sample temperature and the time of effective irradiation. The sample, immersed in a fixative solution of 1% paraformaldehyde (PFA) in PBS, was irradiated for only 10 minutes. The sample temperature did not exceed 37 degrees C. In these mild conditions, the quality of the (ultra)structural preservation of the samples, morphometrically assessed, was at the same level as obtained with the same fixative, using conventional methods. On the contrary, samples fixed in the same conditions without irradiation showed a poor structural preservation. The antigenic preservation of the irradiated samples was excellent, since the labeling levels of two nucleolar proteins, detected by immunogold, were three times higher than in conventionally fixed samples. In the so-called microwave bench, the pathway of microwaves is guided, so that low-power microwaves directly hit the sample and there is no dispersion of energy. Temperature of fixative did not increase after microwave irradiation. Fixation in the bench with either 4% PFA, or 1% PFA, for 20 minutes resulted in structural preservation of samples similar in quality as obtained with conventional fixation and in a similar or better level of antigen preservation. Therefore, controlling temperature and effective irradiation is crucial in order to obtain optimal structural and antigen preservation with microwave-enhanced fixation. The dramatic differences observed between microwave-irradiated samples and samples fixed in the same conditions without irradiation, strongly support the existence of specific effects of microwaves on fixation, independent from the mere heating of the samples.
我们探索了微波技术在固定方面的应用,目的是实现更快的固定方案、降低有毒挥发性试剂的浓度并增强抗原检测。我们使用了一台改装的家用微波炉(900瓦)和一个低功率(5瓦)的微波实验台。实验材料为植物材料。该微波炉配备了冷却装置、搅拌系统以及样品温度和有效辐照时间的记录装置。将样品浸入含1%多聚甲醛(PFA)的PBS固定液中,仅辐照10分钟。样品温度未超过37摄氏度。在这些温和条件下,通过形态计量学评估,样品的(超)结构保存质量与使用相同固定剂的传统方法所获得的水平相当。相反,在相同条件下未辐照固定的样品结构保存较差。辐照样品的抗原保存效果极佳,因为通过免疫金检测的两种核仁蛋白的标记水平比传统固定样品高出三倍。在所谓的微波实验台中,微波路径是有导向的,这样低功率微波能直接作用于样品且能量无分散。微波辐照后固定液温度未升高。在实验台中用4% PFA或1% PFA固定20分钟,样品的结构保存质量与传统固定相似且抗原保存水平相当或更好。因此,为了通过微波增强固定获得最佳的结构和抗原保存效果,控制温度和有效辐照至关重要。在微波辐照样品与相同条件下未辐照固定的样品之间观察到的显著差异,有力地支持了微波对固定存在特定作用,这与仅仅对样品加热无关。