利用PNMT启动子在转基因小鼠中靶向肿瘤生成永生化神经元和神经内分泌细胞系

J. Hammang, E. Baetge, A. Messing
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引用次数: 1

摘要

摘要苯乙醇胺n -甲基转移酶(Phenylethanolamine N-methyltransferase, PNMT)是儿茶酚胺生物合成途径的末端酶,将去甲肾上腺素转化为肾上腺素。在转基因小鼠中,2 kb的人类PNMT启动子可在三类视网膜神经元和肾上腺髓质染色质细胞中指导类人猿病毒40 (sv40)早期区域的表达。这些转基因动物在3至4个月大时出现视网膜和肾上腺髓质肿瘤。我们已经使这些肿瘤细胞适应细胞培养,并获得了永生化的视网膜神经元和肾上腺染色质细胞系。这些细胞系表达许多细胞和组织特异性标记,表明分化的细胞来源。
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Immortalized Neuronal and Neuroendocrine Cell Lines by Targeted Oncogenesis in Transgenic Mice Using the PNMT Promoter
Abstract Phenylethanolamine N-methyltransferase (PNMT) is the terminal enzyme in the catecholamine biosynthetic pathway, converting norepinephrine to epinephrine. In transgenic mice, 2 kb of the human PNMT promoter directs the expression of the simian virus 40 (SV4O) early region in three classes of retinal neurons and in chromaffin cells of the adrenal medulla. These transgenic animals develop retinal and adrenal medullary tumors between 3 and 4 months of age. We have adapted these tumor cells to cell culture and have derived immortalized retinal neuronal and adrenal chromaffin cell lines. These cell lines express a number of cell- and tissue-specific markers indicative of the differentiated cells of origin.
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