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Optical sectioning deep inside live embryos by selective plane illumination microscopy

机译:通过选择性平面照明显微镜对活胚胎内部进行光学切片

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Large, living biological specimens present challenges to existing optical imaging techniques because of their absorptive and scattering properties. We developed selective plane illumination microscopy (SPIM) to generate multidimensional images of samples up to a few millimeters in size. The system combines two-dimensional illumination with orthogonal camera-based detection to achieve high-resolution, optically sectioned imaging throughout the sample, with minimal photodamage and at speeds capable of capturing transient biological phenomena. We used SPIM to visualize all muscles in vivo in the transgenic Medaka line Arnie, which expresses green fluorescent protein in muscle tissue. We also demonstrate that SPIM can be applied to visualize the embryogenesis of the relatively opaque Drosophila melanogaster in vivo.
机译:大型的活生物标本由于其吸收和散射特性,对现有的光学成像技术提出了挑战。我们开发了选择性平面照明显微镜(SPIM)来生成尺寸高达几毫米的样本的多维图像。该系统将二维照明与基于正交相机的检测相结合,以最小的光损伤和能够捕获瞬态生物学现象的速度实现整个样品的高分辨率,光学切片成像。我们使用SPIM可视化了转基因Medaka系Arnie中体内的所有肌肉,该系在肌肉组织中表达绿色荧光蛋白。我们还证明了SPIM可以用于可视化体内相对不透明的果蝇的胚胎发生。

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