Lu Fa-Ke, Basu Srinjan, Igras Vivien, Hoang Mai P, Ji Minbiao, Fu Dan, Holtom Gary R, Neel Victor A, Freudiger Christian W, Fisher David E, Xie X Sunney
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138;
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138;
Proc Natl Acad Sci U S A. 2015 Sep 15;112(37):11624-9. doi: 10.1073/pnas.1515121112. Epub 2015 Aug 31.
Label-free DNA imaging is highly desirable in biology and medicine to perform live imaging without affecting cell function and to obtain instant histological tissue examination during surgical procedures. Here we show a label-free DNA imaging method with stimulated Raman scattering (SRS) microscopy for visualization of the cell nuclei in live animals and intact fresh human tissues with subcellular resolution. Relying on the distinct Raman spectral features of the carbon-hydrogen bonds in DNA, the distribution of DNA is retrieved from the strong background of proteins and lipids by linear decomposition of SRS images at three optimally selected Raman shifts. Based on changes on DNA condensation in the nucleus, we were able to capture chromosome dynamics during cell division both in vitro and in vivo. We tracked mouse skin cell proliferation, induced by drug treatment, through in vivo counting of the mitotic rate. Furthermore, we demonstrated a label-free histology method for human skin cancer diagnosis that provides comparable results to other conventional tissue staining methods such as H&E. Our approach exhibits higher sensitivity than SRS imaging of DNA in the fingerprint spectral region. Compared with spontaneous Raman imaging of DNA, our approach is three orders of magnitude faster, allowing both chromatin dynamic studies and label-free optical histology in real time.
无标记DNA成像在生物学和医学领域非常重要,它能够在不影响细胞功能的情况下进行实时成像,并在手术过程中获得即时的组织学检查结果。在此,我们展示了一种基于受激拉曼散射(SRS)显微镜的无标记DNA成像方法,可在活体动物和完整的新鲜人体组织中以亚细胞分辨率可视化细胞核。依靠DNA中碳氢键独特的拉曼光谱特征,通过在三个最佳选择的拉曼位移处对SRS图像进行线性分解,从蛋白质和脂质的强背景中获取DNA的分布。基于细胞核中DNA凝聚的变化,我们能够在体外和体内捕捉细胞分裂过程中的染色体动态。我们通过体内有丝分裂率计数追踪了药物治疗诱导的小鼠皮肤细胞增殖。此外,我们展示了一种用于人类皮肤癌诊断的无标记组织学方法,其结果与苏木精和伊红(H&E)等其他传统组织染色方法相当。我们的方法在指纹光谱区域对DNA的SRS成像具有更高的灵敏度。与DNA的自发拉曼成像相比,我们的方法快三个数量级,能够实时进行染色质动态研究和无标记光学组织学分析。