Zhao Youbo, Bower Andrew J, Graf Benedikt W, Boppart Marni D, Boppart Stephen A
Biophotonics Imaging Laboratory, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Methods Mol Biol. 2013;1052:57-76. doi: 10.1007/7651_2013_28.
Bone marrow (BM)-derived stem and immune cells play critical roles in maintaining the health, regeneration, and repair of many tissues. Given their important functions in tissue regeneration and therapy, tracking the dynamic behaviors of BM-derived cells has been a long-standing research goal of both biologists and engineers. Because of the complex cellular-level processes involved, real-time imaging technologies that have sufficient spatial and temporal resolution to visualize them are needed. In addition, in order to track cellular dynamics, special attention is needed to account for changes in the microenvironment where the cells reside, for example, tissue contraction, stretching, development, etc. In this chapter, we introduce methods for real-time imaging and longitudinal tracking of BM-derived immune and stem cells in in vivo three-dimensional (3-D) tissue environments with an integrated optical microscope. The integrated microscope combines multiple imaging functions derived from optical coherence tomography (OCT) and multiphoton microscopy (MPM), including optical coherence microscopy (OCM), microvasculature imaging, two-photon excited fluorescence (TPEF), and second harmonic generation (SHG) microscopy. Short- and long-term tracking of the dynamic behavior of BM-derived cells involved in cutaneous wound healing and skin grafting in green fluorescent protein (GFP) BM-transplanted mice is demonstrated. Methods and algorithms for nonrigid registration of time-lapse images are introduced, which allows for long-term tracking of cell dynamics over several months.
骨髓(BM)来源的干细胞和免疫细胞在维持许多组织的健康、再生和修复中发挥着关键作用。鉴于它们在组织再生和治疗中的重要功能,追踪BM来源细胞的动态行为一直是生物学家和工程师长期以来的研究目标。由于涉及复杂的细胞水平过程,因此需要具有足够空间和时间分辨率以对其进行可视化的实时成像技术。此外,为了追踪细胞动态,需要特别关注细胞所处微环境的变化,例如组织收缩、拉伸、发育等。在本章中,我们介绍了使用集成光学显微镜在体内三维(3-D)组织环境中对BM来源的免疫细胞和干细胞进行实时成像和纵向追踪的方法。该集成显微镜结合了源自光学相干断层扫描(OCT)和多光子显微镜(MPM)的多种成像功能,包括光学相干显微镜(OCM)、微血管成像、双光子激发荧光(TPEF)和二次谐波产生(SHG)显微镜。展示了对绿色荧光蛋白(GFP)BM移植小鼠中参与皮肤伤口愈合和皮肤移植的BM来源细胞动态行为的短期和长期追踪。介绍了用于延时图像非刚性配准的方法和算法,这使得能够对细胞动态进行长达数月的长期追踪。