Meng Fanwei, Shi Ling, Cheng Xuan, Hou Ning, Wang Yongliang, Teng Yan, Meng Anming, Yang Xiao
Genetic Laboratory of Development and Diseases, Institute of Biotechnology, Beijing, PR China.
Matrix Biol. 2007 Jan;26(1):54-7. doi: 10.1016/j.matbio.2006.09.003. Epub 2006 Sep 16.
Brain microvascular endothelial cells (ECs) have unique characteristics distinguished from peripheral ECs and play important roles in blood-brain barrier (BBB). To investigate the physiological control of the brain ECs, we generated a transgenic mouse line in which the expression of Cre recombinase was driven by the promoter of the mouse surfactant protein A (SP-A) gene. The Cre activity was detected in blood vessels of brain, alveolar type II cells of lung and epithelium of gland stomach. In brain ECs, the Cre activity started at embryonic day 11.5, indicating that the subpopulation of ECs in brain could be molecularly defined at early embryonic stages. The use of SP-A-Cre mice should facilitate analysis of gene function in the brain ECs.
脑微血管内皮细胞(ECs)具有与外周内皮细胞不同的独特特征,在血脑屏障(BBB)中发挥重要作用。为了研究脑内皮细胞的生理调控,我们构建了一种转基因小鼠品系,其中Cre重组酶的表达由小鼠表面活性蛋白A(SP-A)基因的启动子驱动。在脑的血管、肺的II型肺泡细胞和腺胃上皮中检测到了Cre活性。在脑内皮细胞中,Cre活性在胚胎第11.5天开始出现,这表明脑内皮细胞亚群在胚胎早期阶段就可以在分子水平上进行定义。使用SP-A-Cre小鼠应有助于分析脑内皮细胞中的基因功能。