Murata Shin-ichi, Herman Petr, Iwashina Masanori, Mochizuki Kunio, Nakazawa Tadao, Kondo Tetsuo, Nakamura Nobuki, Lakowicz Joseph R, Katoh Ryohei
University of Yamanashi, Interdisciplinary Graduate School of Medicine and Engineering, Department of Pathology, Yamanashi, Japan.
J Biomed Opt. 2005 May-Jun;10(3):034008. doi: 10.1117/1.1924667.
We propose a novel application of microscopic Forster resonance energy transfer (FRET) to clinical cytological diagnosis based on sensitive measurements of distance changes between fluorescently labeled deoxyribose nucleic acid (DNA) molecules. We have employed the microscopic FRET imaging for investigation of six papillary carcinomas and eight benign cases. In each case the FRET images of 20 cells stained by the AT-specific donor Hoechst 33258 and the GC-specific acceptor 7-aminoactinomycin D were acquired and analyzed by texture analysis. We have not found significant difference of the mean FRET efficiency between the benign and malignant groups. On the other hand, the texture analysis revealed a significant difference of the intranuclear spatial distribution of FRET efficiencies between the benign and malignant groups. The results indicate that despite the similar average distance between the AT- and the GC-rich DNA segments in the papillary carcinomas and the benign cases, the former has more heterogeneous distribution of the AT- and the GC-rich DNA segments in nuclei compared to the benign groups. We have demonstrated that the FRET imaging is a helpful tool for the medical cytological diagnosis of human tumors by giving information on the chromatin topology on the scale below the resolution of conventional optical microscopes. (c) 2005 Society of Photo-Optical Instrumentation Engineers.
我们基于对荧光标记的脱氧核糖核酸(DNA)分子间距离变化的灵敏测量,提出一种将微观Förster共振能量转移(FRET)应用于临床细胞学诊断的新方法。我们已采用微观FRET成像对6例乳头状癌和8例良性病例进行研究。在每个病例中,获取了用AT特异性供体Hoechst 33258和GC特异性受体7-氨基放线菌素D染色的20个细胞的FRET图像,并通过纹理分析进行分析。我们未发现良性和恶性组之间平均FRET效率有显著差异。另一方面,纹理分析显示良性和恶性组之间FRET效率的核内空间分布存在显著差异。结果表明,尽管乳头状癌和良性病例中富含AT和富含GC的DNA片段之间的平均距离相似,但与良性组相比,前者核内富含AT和富含GC的DNA片段分布更不均匀。我们已证明,FRET成像通过提供传统光学显微镜分辨率以下尺度的染色质拓扑结构信息,是人类肿瘤医学细胞学诊断的一种有用工具。(c)2005年光电仪器工程师协会。