Parma A M, Marangos P J, Goodwin F K
J Neurochem. 1981 Mar;36(3):1093-6. doi: 10.1111/j.1471-4159.1981.tb01704.x.
Neuron-specific enolase (NSE) and non-neuronal enolase (NNE) have been shown to be highly specific neuronal and glial products respectively and are therefore useful as biochemical markers of the two major cell types in the vertebrate central nervous system. An iodinated radioimmunoassay (RIA) procedure for human NSE (NSE-H) with approximately 50-fold greater sensitivity than the previously available tritiated assay is described. This assay is capable of detecting 100 pg of NSE-H per assay. NSE levels in human cerebrospinal fluid (CSF) which were previously undetectable with the tritiated RIA are now easily measured and have been shown to be approximately 2 ng/ml of CSF. Furthermore, results obtained with the newly described assay procedure on more concentrated brain tissue extracts are comparable to the tritiated RIA. The iodinated NSE RIA is also shown to be capable of accurately detecting added amounts of NSE in human CSF, indicating the potential clinical usefulness of this assay in determining elevated levels of NSE in CSF.
神经元特异性烯醇化酶(NSE)和非神经元烯醇化酶(NNE)已分别被证明是高度特异性的神经元和神经胶质细胞产物,因此可用作脊椎动物中枢神经系统中两种主要细胞类型的生化标志物。本文描述了一种用于检测人NSE(NSE-H)的碘化放射免疫分析(RIA)方法,其灵敏度比之前可用的氚化分析方法高约50倍。该分析方法每次检测能够检测到100 pg的NSE-H。人脑脊液(CSF)中的NSE水平以前用氚化RIA无法检测到,现在很容易测量,结果显示约为2 ng/ml CSF。此外,用新描述的分析方法对更浓缩的脑组织提取物进行检测得到的结果与氚化RIA相当。碘化NSE RIA还被证明能够准确检测人CSF中添加的NSE量,表明该分析方法在确定CSF中NSE水平升高方面具有潜在的临床应用价值。