Lorca-Cámara Antonio, Tourain Christophe, de Sars Vincent, Emiliani Valentina, Accanto Nicolò
Sorbonne Université, INSERM, CNRS, Institut de la Vision, 75012 Paris, France.
Biomed Opt Express. 2024 Mar 4;15(4):2094-2109. doi: 10.1364/BOE.507690. eCollection 2024 Apr 1.
The development of efficient genetically encoded indicators and actuators has opened up the possibility of reading and manipulating neuronal activity in living tissues with light. To achieve precise and reconfigurable targeting of large numbers of neurons with single-cell resolution within arbitrary volumes, different groups have recently developed all-optical strategies based on two-photon excitation and spatio-temporal shaping of ultrashort laser pulses. However, such techniques are often complex to set up and typically operate at a single wavelength only. To address these issues, we have developed a novel optical approach that uses a fiber bundle and a spatial light modulator to achieve simple and dual-color two-photon light patterning in three dimensions. By leveraging the core-to-core temporal delay and the wavelength-independent divergence characteristics of fiber bundles, we have demonstrated the capacity to generate high-resolution excitation spots in a 3D region with two distinct laser wavelengths simultaneously, offering a suitable and simple alternative for precise multicolor cell targeting.
高效的基因编码指示剂和驱动器的发展,为利用光读取和操纵活组织中的神经元活动开辟了可能性。为了在任意体积内以单细胞分辨率实现对大量神经元的精确且可重构靶向,不同研究团队最近基于双光子激发和超短激光脉冲的时空整形开发了全光学策略。然而,此类技术通常设置复杂,且通常仅在单一波长下运行。为了解决这些问题,我们开发了一种新颖的光学方法,该方法使用光纤束和空间光调制器在三维空间中实现简单的双色双光子光图案化。通过利用光纤束的纤芯到纤芯的时间延迟和与波长无关的发散特性,我们展示了同时使用两种不同激光波长在三维区域中生成高分辨率激发点的能力,为精确的多色细胞靶向提供了一种合适且简单的替代方法。