Shan Liang, Zhang Renshu, Zhang Wanghai, Lee Edward, Sridhar Rajagopalan, Snyderwine Elizabeth G, Wang Paul C
Department of Radiology, Howard University, Washington, DC 20060, USA.
Anal Biochem. 2008 Nov 15;382(2):122-8. doi: 10.1016/j.ab.2008.08.004. Epub 2008 Aug 8.
We have developed an image-based technique for signal pathway analysis, target validation, and compound screening related to mammary epithelial cell differentiation. This technique used the advantages of optical imaging and the HC11-Lux model system. The HC11-Lux cell line is a subclone of HC11 mammary epithelial cells transfected stably with a luciferase construct of the beta-casein gene promoter (p-344/-1betac-Lux). The promoter activity was imaged optically in real time following lactogenic induction. The imaging signal intensity was closely correlated with that measured using a luminometer following protein extraction (R=0.99, P<0.0001) and consistent with the messenger RNA (mRNA) level of the endogenous beta -casein gene. Using this technique, we examined the roles of JAK2/Stat5A, Raf-1/MEK/MAKP, and PI3K/Akt signal pathways with respect to differentiation. The imaging studies showed that treatment of the cells with epidermal growth factor (EGF), AG490 (JAK2-specific inhibitor), and LY294002 (PI3K-specific inhibitor) blocked lactogenic differentiation in a dose-dependent manner. PD98059 (MEK-specific inhibitor) could reverse EGF-mediated differentiation arrest. These results indicate that these pathways are essential in cell differentiation. This simple, sensitive, and reproducible technique permits visualization and real-time evaluation of the molecular events related to milk protein production. It can be adopted for high-throughput screening of small molecules for their effects on mammary epithelial cell growth, differentiation, and carcinogenesis.
我们开发了一种基于图像的技术,用于与乳腺上皮细胞分化相关的信号通路分析、靶点验证和化合物筛选。该技术利用了光学成像和HC11-Lux模型系统的优势。HC11-Lux细胞系是HC11乳腺上皮细胞的一个亚克隆,它被稳定转染了β-酪蛋白基因启动子(p-344/-1betac-Lux)的荧光素酶构建体。在泌乳诱导后,通过光学实时成像启动子活性。成像信号强度与蛋白质提取后使用光度计测量的信号强度密切相关(R = 0.99,P < 0.0001),并且与内源性β-酪蛋白基因的信使RNA(mRNA)水平一致。使用该技术,我们研究了JAK2/Stat5A、Raf-1/MEK/MAKP和PI3K/Akt信号通路在分化方面的作用。成像研究表明,用表皮生长因子(EGF)、AG490(JAK2特异性抑制剂)和LY294002(PI3K特异性抑制剂)处理细胞会以剂量依赖性方式阻断泌乳分化。PD98059(MEK特异性抑制剂)可以逆转EGF介导的分化停滞。这些结果表明这些通路在细胞分化中至关重要。这种简单、灵敏且可重复的技术允许可视化和实时评估与乳蛋白产生相关的分子事件。它可用于高通量筛选小分子对乳腺上皮细胞生长、分化和致癌作用的影响。