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一种在新生大脑中富集的脑特异性抗原的鉴定与特性研究。II. 抗原稳定性、种属交叉反应性及肿瘤细胞关联

Identification and characterization of a brain-specific antigen enriched in neonatal brain. II. Antigenic stability, species cross-reactivity and tumor cell association.

作者信息

Strong D D, Herschman H R

出版信息

Brain Res. 1980 Feb 24;184(2):271-82. doi: 10.1016/0006-8993(80)90798-2.

DOI:10.1016/0006-8993(80)90798-2
PMID:6766343
Abstract

NABSA is a brain-specific antigen enriched in neonatal brain. Microcomplement fixation was used to determine the extent of serological stability of NABSA towards heat denaturation and freeze-thaw denaturation. NABSA antigenic activity was progressively lost from neonatal and adult brain solutions incubated at temperatures above 40 degrees C. All activity was lost above 65 degrees C. Dilute solutions of NABSA were stable at 8 degrees C for at least two weeks and could be frozen and thawed in Tris.phosphate buffer at concentrations above 2 mg/ml with little loss of activity. NABSA was found in every vertebrate species tested. An unusually close structural similarity (a frequent characteristic of both brain-specific antigens and fetal antigens) was demonstrated by serological methods among the mammalian and avian NABSAs. NABSA was detected by microcomplement fixation analysis in 4 out of 16 rat and murine neural clonal tumor cell lines. There was no clear limitation of NABSA to a particular class of neural cell (as defined by the phenotypes of these tumor cell classes) or to rapidly dividing or stationary phase cells. NABSA may be a brain-specific oncofetal antigen (OFA-associated), since it is present in tumor cells of the nervous system and high levels are found in immature brain.

摘要

NABSA是一种在新生大脑中富集的脑特异性抗原。采用微量补体结合法来确定NABSA对热变性和冻融变性的血清学稳定性程度。在40摄氏度以上孵育的新生和成年脑溶液中,NABSA的抗原活性逐渐丧失。在65摄氏度以上时所有活性均丧失。NABSA的稀释溶液在8摄氏度下至少两周保持稳定,并且在浓度高于2mg/ml的磷酸三缓冲液中冻融时活性损失很小。在所测试的每一种脊椎动物物种中都发现了NABSA。通过血清学方法在哺乳动物和鸟类的NABSA之间证明了一种异常紧密的结构相似性(这是脑特异性抗原和胎儿抗原的常见特征)。通过微量补体结合分析在16种大鼠和小鼠神经克隆肿瘤细胞系中的4种中检测到了NABSA。NABSA对特定类别的神经细胞(由这些肿瘤细胞类别的表型定义)或对快速分裂或静止期细胞没有明显的限制。NABSA可能是一种脑特异性肿瘤胎儿抗原(与OFA相关),因为它存在于神经系统的肿瘤细胞中,并且在未成熟大脑中含量很高。

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