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Two-Photon Fluorescence Microscopy and Applications in Angiogenesis and Related Molecular Events

荧光显微镜 双光子激发显微术 显微镜 血管生成 显微镜 分子成像 荧光寿命成像显微镜 病理 生物 荧光 体内 医学 光学 物理 生物技术 癌症研究
作者
Lee M,Sathya Kannan,Giridharan Muniraj,Vinícius Rosa,Wen Feng Lu,Jerry Ying Hsi Fuh,Gopu Sriram,Tong Cao
出处
期刊:Tissue Engineering Part B-reviews [Mary Ann Liebert, Inc.]
卷期号:28 (4): 926-937 被引量:12
标识
DOI:10.1089/ten.teb.2021.0140
摘要

The role of angiogenesis in health and disease have gained considerable momentum in recent years. Visualizing angiogenic patterns and associated events of surrounding vascular beds in response to therapeutic and laboratory-grade biomolecules has become a commonplace in regenerative medicine and the biosciences. To achieve high-quality imaging for elucidating the molecular mechanisms of angiogenesis, the two-photon excitation fluorescence (2PEF) microscopy, or multiphoton fluorescence microscopy is increasingly utilized in scientific investigations. The 2PEF microscope confers several distinct imaging advantages over other fluorescence excitation microscopy techniques—for the observation of in-depth, three-dimensional vascularity in a variety of tissue formats, including fixed tissue specimens and in vivo vasculature in live specimens. Understanding morphological and subcellular changes that occur in cells and tissues during angiogenesis will provide insights to behavioral responses in diseased states, advance the engineering of physiologically relevant tissue models, and provide biochemical clues for the design of therapeutic strategies. We review the applicability and limitations of the 2PEF microscope on the biophysical and molecular-level signatures of angiogenesis in various tissue models. Imaging techniques and strategies for best practices in 2PEF microscopy will be reviewed. Deep live tissue imaging provides unique opportunities to study angiogenesis and associated events in real-time. In contrast to cross-sectional data provided by conventional methods, two-photon microscopy enables high-resolution tissue imaging, data acquisition over time, real-time visualization of angiogenic events, and reduces the number of animal models used in scientific research. This review provides insights on different two-photon microscopy methods and its application in live and deep tissue imaging of angiogenesis on in vitro and in vivo tissues. We believe that the current trends in imaging can transform the investigation of angiogenesis, cancer research, and biofabrication of vascularized tissues.
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