Hoffman Robert M
AntiCancer, Inc., Department of Surgery, University of California San Diego, San Diego, CA, USA.
Lab Invest. 2015 Apr;95(4):432-52. doi: 10.1038/labinvest.2014.154. Epub 2015 Feb 16.
Multicolored proteins have allowed the color-coding of cancer cells growing in vivo and enabled the distinction of host from tumor with single-cell resolution. Non-invasive imaging with fluorescent proteins enabled the dynamics of metastatic cancer to be followed in real time in individual animals. Non-invasive imaging of cancer cells expressing fluorescent proteins has allowed the real-time determination of efficacy of candidate antitumor and antimetastatic agents in mouse models. The use of fluorescent proteins to differentially label cancer cells in the nucleus and cytoplasm can visualize the nuclear-cytoplasmic dynamics of cancer cells in vivo including: mitosis, apoptosis, cell-cycle position, and differential behavior of nucleus and cytoplasm that occurs during cancer-cell deformation and extravasation. Recent applications of the technology described here include linking fluorescent proteins with cell-cycle-specific proteins such that the cells change color from red to green as they transit from G1 to S phases. With the macro- and micro-imaging technologies described here, essentially any in vivo process can be imaged, giving rise to the new field of in vivo cell biology using fluorescent proteins.
多色蛋白实现了对体内生长的癌细胞进行颜色编码,并能够以单细胞分辨率区分宿主细胞和肿瘤细胞。利用荧光蛋白进行的非侵入性成像能够实时追踪个体动物体内转移性癌症的动态变化。对表达荧光蛋白的癌细胞进行非侵入性成像,能够在小鼠模型中实时测定候选抗肿瘤和抗转移药物的疗效。利用荧光蛋白对细胞核和细胞质中的癌细胞进行差异标记,可以在体内可视化癌细胞的核质动态变化,包括:有丝分裂、凋亡、细胞周期位置,以及癌细胞变形和外渗过程中细胞核和细胞质的差异行为。此处所述技术的最新应用包括将荧光蛋白与细胞周期特异性蛋白连接起来,使细胞在从G1期过渡到S期时颜色从红色变为绿色。借助此处所述的宏观和微观成像技术,基本上任何体内过程都可以成像,从而催生了利用荧光蛋白的体内细胞生物学新领域。