Chaudhuri A, Zangenehpour S, Rahbar-Dehgan F, Ye F
Department of Psychology, McGill University, Montreal, QC, Canada.
Acta Neurobiol Exp (Wars). 2000;60(3):403-10. doi: 10.55782/ane-2000-1359.
The rapid accumulation of inducible transcription factors (ITFs), such as c-Fos and Zif268, in activated neurons combined with histological methods that offer detection at the cellular level are key features that have led to their wide use in visualizing activated neurons. There are two major drawbacks of ITFs that limit their use in the CNS--cell-type expression specificity and stimulus-transcription coupling uncertainty. Recent technical advances in the field of molecular activity mapping now permit dual-labeling approaches that help resolve some of these ambiguities and identify neurons that are activated by different sensory stimuli. Furthermore, the recent identification of the robl/LC7-like gene, which shows immediate-early repression after stimulation, may have utility in functional mapping where it can be used to delineate quiescent neurons and serve as a complement to molecular activity markers.
诱导型转录因子(ITFs),如c-Fos和Zif268,在激活的神经元中迅速积累,再结合能够在细胞水平进行检测的组织学方法,这些关键特性使得它们在可视化激活神经元方面得到广泛应用。ITFs存在两个主要缺点,限制了它们在中枢神经系统中的应用——细胞类型表达特异性和刺激-转录偶联不确定性。分子活性图谱领域的最新技术进展现在允许采用双标记方法,有助于解决其中一些模糊性问题,并识别由不同感觉刺激激活的神经元。此外,最近发现的robl/LC7样基因,在刺激后表现出即时早期抑制,可能在功能图谱绘制中有用,可用于描绘静止神经元,并作为分子活性标记的补充。