Department of Biochemistry, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Nat Methods. 2010 Jan;7(1):67-73. doi: 10.1038/nmeth.1405. Epub 2009 Dec 6.
Apoptosis is of central importance to many areas of biological research, but there is a lack of methods that permit continuous monitoring of apoptosis or cell viability in a nontoxic and noninvasive manner. Here we report the development of a tool applicable to live-cell imaging that facilitates the visualization of real-time apoptotic changes without perturbing the cellular environment. We designed a polarity-sensitive annexin-based biosensor (pSIVA) with switchable fluorescence states, which allows detection only when bound to apoptotic cells. Using pSIVA with live-cell imaging, we observed dynamic local changes in individual rat neurons during degeneration in vitro and in vivo. Furthermore, we observed that pSIVA binding was reversible and clearly defined the critical period for neurons to be rescued. We anticipate pSIVA can be widely applied to address questions concerning spatiotemporal events in apoptotic processes, its reversibility and the general viability of cells in culture.
细胞凋亡在许多生物学研究领域都具有重要意义,但目前缺乏能够以无毒、非侵入的方式持续监测细胞凋亡或细胞活力的方法。在这里,我们报告了一种适用于活细胞成像的工具的开发,该工具可以在不干扰细胞环境的情况下促进实时凋亡变化的可视化。我们设计了一种具有可切换荧光状态的、基于 Annexin 的极性敏感生物传感器(pSIVA),只有与凋亡细胞结合时才能被检测到。使用 pSIVA 进行活细胞成像,我们观察到体外和体内培养的单个大鼠神经元在变性过程中动态的局部变化。此外,我们观察到 pSIVA 结合是可逆的,并明确了神经元可以被挽救的关键时期。我们预计 pSIVA 可以广泛应用于解决与凋亡过程中的时空事件、其可逆性以及培养细胞的一般活力有关的问题。