Long-term time-lapse multimodal intravital imaging of regeneration and bone-marrow-derived cell dynamics in skin.

Benedikt W Graf, Eric J Chaney, Marina Marjanovic, Steven G Adie, Michael De Lisio, M Carmen Valero, Marni D Boppart, Stephen A Boppart
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引用次数: 20

Abstract

A major challenge for translating cell-based therapies is understanding the dynamics of cells and cell populations in complex in vivo environments. Intravital microscopy has shown great promise for directly visualizing cell behavior in vivo. However, current methods are limited to relatively short imaging times (hours), by ways to track cell and cell population dynamics over extended time-lapse periods (days to weeks to months), and by relatively few imaging contrast mechanisms that persist over extended investigations. We present technology to visualize and quantify complex, multifaceted dynamic changes in natural deformable skin over long time periods using novel multimodal imaging and a non-rigid image registration method. These are demonstrated in green fluorescent protein (GFP) bone marrow (BM) transplanted mice to study dynamic skin regeneration. This technology provides a novel perspective for studying dynamic biological processes and will enable future studies of stem, immune, and tumor cell biology in vivo.

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皮肤再生和骨髓源性细胞动力学的长期延时多模态活体成像。
翻译细胞疗法的一个主要挑战是理解复杂体内环境中细胞和细胞群的动力学。活体显微术在直接观察细胞在体内的行为方面显示出很大的前景。然而,目前的方法仅限于相对较短的成像时间(小时),通过在较长的时间间隔内(几天到几周到几个月)跟踪细胞和细胞群体动态的方法,以及相对较少的在长期调查中持续存在的成像对比机制。我们提出的技术可视化和量化复杂的,多方面的动态变化,自然变形的皮肤在很长一段时间内使用新颖的多模态成像和非刚性图像配准方法。这些在绿色荧光蛋白(GFP)骨髓(BM)移植小鼠中得到证实,以研究动态皮肤再生。这项技术为研究动态生物过程提供了一个新的视角,并将使未来的干细胞、免疫和肿瘤细胞生物学的体内研究成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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