Hayashi Koichiro, Sato Yusuke, Maruoka Hiroki, Sakamoto Wataru, Yogo Toshinobu
Division of Materials Research, Institute of Materials and Systems for Sustainability, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.
Technical Research Laboratory Applied Development Group, Kurabo Industries Ltd., 14-30, Shimokido-Cho, Neyagawa, Osaka 572-0823, Japan.
ACS Biomater Sci Eng. 2017 Jun 12;3(6):1129-1135. doi: 10.1021/acsbiomaterials.7b00181. Epub 2017 Apr 24.
Techniques to elucidate the kinetics and distribution of the same cells in the whole body and in tissues are necessary for further studies of cancer, immunity, and regenerative medicine. Fluorescent imaging is a powerful technique for visualization of cells. However, current fluorescent probes are applicable in either the ultraviolet (UV)-visible (Vis) region (300-650 nm) or the biological transparency window (BTW, 650-900 nm), but not both. Thus, they cannot serve as fluorescent probes for both in vivo and in vitro imaging, and it is difficult to achieve imaging of the same cells seamlessly from the cellular level to the whole body and tissue levels using currently available fluorescent probes. Accordingly, in this paper, we describe organic-inorganic hybrid nanoparticles (HNPs) that could be used to achieve seamless tracking of the same cells. Within the HNPs, a porphyrin molecule, Vis-fluorophore, was surrounded by a siloxane chain, preventing the aggregation of porphyrin molecules. As a result, the porphyrin fluorescence was not quenched. Furthermore, indocyanine green (ICG), a BTW fluorophore, was localized on the HNP surface, leading to fluorescence resonance energy transfer (FRET) from porphyrin to ICG only near the HNP surface. Through the above structural design, the HNPs acquired both excitation (λ) and emission (λ) wavelengths in the visible region and BTW, respectively, as well as large Stokes shifts. The HNP-labeled immune cells successfully and the labeled cells were separated easily from unlabeled cells by fluorescence-activated cell sorting. The kinetics of the labeled cells in the whole body were revealed by fluorescence imaging within BTW. Furthermore, the distributions of the same labeled cells were elucidated by histological analysis within the UV-vis region. Thus, the HNPs served as fluorescent probes for seamless tracking of the same cells.
阐明同一细胞在全身和组织中的动力学及分布的技术,对于癌症、免疫和再生医学的进一步研究是必要的。荧光成像技术是一种强大的细胞可视化技术。然而,目前的荧光探针仅适用于紫外(UV)-可见(Vis)区域(300-650nm)或生物透明窗口(BTW,650-900nm),不能同时适用于这两个区域。因此,它们不能作为体内和体外成像的荧光探针,并且使用现有的荧光探针很难实现从细胞水平到全身和组织水平的同一细胞的无缝成像。因此,在本文中,我们描述了一种可用于实现同一细胞无缝追踪的有机-无机杂化纳米颗粒(HNP)。在HNP中,卟啉分子(一种可见荧光团)被硅氧烷链包围,防止了卟啉分子的聚集。结果,卟啉荧光没有淬灭。此外,吲哚菁绿(ICG,一种BTW荧光团)定位在HNP表面,导致仅在HNP表面附近发生从卟啉到ICG的荧光共振能量转移(FRET)。通过上述结构设计,HNP分别在可见光区域和BTW获得了激发(λ)和发射(λ)波长,以及大的斯托克斯位移。用HNP标记免疫细胞获得成功,并且通过荧光激活细胞分选很容易将标记细胞与未标记细胞分离。通过BTW内的荧光成像揭示了标记细胞在全身的动力学。此外,通过紫外-可见区域内的组织学分析阐明了相同标记细胞的分布。因此,HNP可作为同一细胞无缝追踪的荧光探针。