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Long-term in vivo single-cell lineage tracing of deep structures using three-photon activation

机译:使用三光子激活的深层结构的长期体内单细胞谱系追踪

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摘要

Genetic labeling techniques allow for noninvasive lineage tracing of cells in vivo. Two-photon inducible activators provide spatial resolution for superficial cells, but labeling cells located deep within tissues is precluded by scattering of the far-red illumination required for two-photon photolysis. Three-photon illumination has been shown to overcome the limitations of two-photon microscopy for in vivo imaging of deep structures, but whether it can be used for photoactivation remains to be tested. Here we show, both theoretically and experimentally, that three-photon illumination overcomes scattering problems by combining longer wavelength excitation with high uncaging three-photon cross-section molecules. We prospectively labeled heart muscle cells in zebrafish embryos and found permanent labeling in their progeny in adult animals with negligible tissue damage. This technique allows for a noninvasive genetic manipulation in vivo with spatial, temporal and cell-type specificity, and may have wide applicability in experimental biology.
机译:遗传标记技术允许在体内对细胞进行无创谱系追踪。双光子诱导型激活剂为浅层细胞提供了空间分辨率,但是通过散射双光子光解所需的远红光,可以排除位于组织深处的标记细胞。三光子照明已被证明克服了深层结构体内成像的两光子显微镜技术的局限性,但是否可用于光激活仍有待检验。在这里我们在理论上和实验上都表明,三光子照明通过将更长的波长激发与高解开的三光子横截面分子相结合,克服了散射问题。我们对斑马鱼胚胎中的心肌细胞进行了前瞻性标记,并在成年动物的后代中发现了永久性标记,其组织损伤可忽略不计。该技术允许在体内进行具有空间,时间和细胞类型特异性的非侵入性遗传操作,并且在实验生物学中可能具有广泛的适用性。

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