Blödorn B, Mäder M, Urade Y, Hayaishi O, Felgenhauer K, Brück W
Department of Neurology of the University, Göttingen, Germany.
Neurosci Lett. 1996 May 10;209(2):117-20. doi: 10.1016/0304-3940(96)12614-8.
Expression of beta-trace protein (beta-trace), recently identified as glutathion-independent prostaglandin D synthase (prostaglandin-H2 D-isomerase; EC 5.3.99.2), was localized in paraffin sections of the human brain by in situ hybridization using digoxigenin-labeled antisense cRNA probes. The mRNA for beta-trace was predominantly found in the epithelial cells of the choroid plexus. Hybridization signals were also obtained in some oligodendrocytes, particularly in the white matter. In the leptomeninges, specific signals were found in meningeal macrophages and in single cells of the arachnoid barrier layer. The cells exhibiting hybridization signals with the antisense cRNA probes for beta-trace were identified by counterstaining with antibodies directed against specific cell markers. Additionally, beta-trace mRNA was localized in tubular epithelial and basal cells of the human epididymis and in different cell types within the seminiferous epithelium of the testis.
β-微球蛋白(β-微球蛋白),最近被鉴定为谷胱甘肽非依赖性前列腺素D合酶(前列腺素-H2 D-异构酶;EC 5.3.99.2),通过使用地高辛标记的反义cRNA探针进行原位杂交,将其定位在人脑石蜡切片中。β-微球蛋白的mRNA主要存在于脉络丛的上皮细胞中。在一些少突胶质细胞中也获得了杂交信号,特别是在白质中。在软脑膜中,在脑膜巨噬细胞和蛛网膜屏障层的单个细胞中发现了特异性信号。通过用针对特定细胞标志物的抗体进行复染,鉴定出与β-微球蛋白反义cRNA探针表现出杂交信号的细胞。此外,β-微球蛋白mRNA定位于人附睾的管状上皮细胞和基底细胞以及睾丸生精上皮内的不同细胞类型中。