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Imaging multicellular specimens with real-time optimized tiling light-sheet selective plane illumination microscopy

机译:使用实时优化平铺光片选择性平面照明显微镜对多细胞标本成像

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摘要

Despite the progress made in selective plane illumination microscopy, high-resolution 3D live imaging of multicellular specimens remains challenging. Tiling light-sheet selective plane illumination microscopy (TLS-SPIM) with real-time light-sheet optimization was developed to respond to the challenge. It improves the 3D imaging ability of SPIM in resolving complex structures and optimizes SPIM live imaging performance by using a real-time adjustable tiling light sheet and creating a flexible compromise between spatial and temporal resolution. We demonstrate the 3D live imaging ability of TLS-SPIM by imaging cellular and subcellular behaviours in live C. elegans and zebrafish embryos, and show how TLS-SPIM can facilitate cell biology research in multicellular specimens by studying left-right symmetry breaking behaviour of C. elegans embryos.
机译:尽管在选择性平面照明显微镜方面取得了进展,但多细胞标本的高分辨率3D实时成像仍然具有挑战性。为了应对这一挑战,开发了具有实时光片优化功能的平铺光片选择性平面照明显微镜(TLS-SPIM)。它通过使用实时可调平铺光片并在空间和时间分辨率之间做出灵活的折衷,提高了SPIM解决复杂结构的3D成像能力,并优化了SPIM实时成像性能。我们通过对秀丽隐杆线虫和斑马鱼胚胎中的细胞和亚细胞行为进行成像来证明TLS-SPIM的3D实时成像能力,并通过研究C的左右对称破坏行为来展示TLS-SPIM如何促进多细胞标本中的细胞生物学研究。线虫的胚胎。

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