Speel E J, Hopman A H, Komminoth P
Department of Pathology, University of Zürich, Zürich, Switzerland.
J Histochem Cytochem. 1999 Mar;47(3):281-8. doi: 10.1177/002215549904700302.
In situ hybridization (ISH) has proved to be an invaluable molecular tool in research and diagnosis to visualize nucleic acids in their cellular environment. However, its applicability can be limited by its restricted detection sensitivity. During the past 10 years, several strategies have been developed to improve the threshold levels of nucleic acid detection in situ by amplification of either target nucleic acid sequences before ISH (e.g., in situ PCR) or the detection signals after the hybridization procedures. Here we outline the principles of tyramide signal amplification using the catalyzed reporter deposition (CARD) technique, present practical suggestions to efficiently enhance the sensitivity of ISH with CARD, and discuss some applications and possible future directions of in situ nucleic acid detection using such an amplification strategy.
原位杂交(ISH)已被证明是一种在研究和诊断中非常有价值的分子工具,可在细胞环境中可视化核酸。然而,其适用性可能受到检测灵敏度受限的限制。在过去10年中,已经开发了几种策略来通过在ISH之前扩增靶核酸序列(例如,原位PCR)或杂交程序之后的检测信号来提高原位核酸检测的阈值水平。在这里,我们概述了使用催化报告沉积(CARD)技术的酪胺信号放大原理,提出了有效提高CARD-ISH灵敏度的实用建议,并讨论了使用这种放大策略进行原位核酸检测的一些应用和可能的未来方向。