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转录共激活因子CBP在大鼠切牙成釉细胞及其他牙釉质器官来源细胞中的定位。

Localization of transcriptional co-activator CBP in the ameloblasts and the other enamel organ-derived cells of the rat incisor.

作者信息

Nishikawa Sumio

机构信息

Department of Biology, Tsurumi University School of Dental Medicine, Yokohama, Japan.

出版信息

J Histochem Cytochem. 2002 Nov;50(11):1455-60. doi: 10.1177/002215540205001104.

Abstract

CREB-binding protein (CBP) was examined in ameloblasts and in other enamel organ-derived cells of the rat incisor, using Western blotting analysis and immunocytochemistry by specific antibodies. Western blotting of labial tissues, including ameloblasts of the incisors, detected a single band with a molecular weight equivalent to the reported value of CBP. In immunocytochemistry, CBP was localized in ameloblast nuclei in the maturation zone but not in the secretion and transition zones. The nuclei of the other enamel organ-derived cells were also positive. Because this protein is suggested to take part in c-Jun-mediated transcription, the present study and the results of a previous report showing c-Jun localization in the nuclei of enamel organ-derived cells suggest that the enamel organ-derived cells, including maturation ameloblasts, undergo active transcriptional regulation.

摘要

利用蛋白质免疫印迹分析和特异性抗体免疫细胞化学技术,对大鼠切牙成釉细胞和其他牙釉质器官来源的细胞中的CREB结合蛋白(CBP)进行了检测。对包括切牙成釉细胞在内的唇侧组织进行蛋白质免疫印迹分析,检测到一条分子量与报道的CBP值相当的单一条带。在免疫细胞化学中,CBP定位于成熟区的成釉细胞核中,而分泌区和过渡区则未检测到。其他牙釉质器官来源的细胞的细胞核也呈阳性。由于该蛋白被认为参与c-Jun介导的转录,本研究以及先前一份显示c-Jun定位于牙釉质器官来源细胞的细胞核中的报告结果表明,包括成熟成釉细胞在内的牙釉质器官来源的细胞经历了活跃的转录调控。

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