活体显微镜检查
双光子激发显微术
显微镜
可视化
多光子荧光显微镜
淋巴
细胞生物学
体内
生物
病理
解剖
计算机科学
光学
荧光显微镜
医学
物理
人工智能
遗传学
荧光
作者
Kibaek Choe,Yusaku Hontani,Tianyu Wang,Eric Hébert,Dimitre G. Ouzounov,Kristine Lai,Ankur Singh,Wendy Béguelin,Ari Melnick,Chris Xu
标识
DOI:10.1038/s41590-021-01101-1
摘要
Intravital confocal microscopy and two-photon microscopy are powerful tools to explore the dynamic behavior of immune cells in mouse lymph nodes (LNs), with penetration depth of ~100 and ~300 μm, respectively. Here, we used intravital three-photon microscopy to visualize the popliteal LN through its entire depth (600-900 μm). We determined the laser average power and pulse energy that caused measurable perturbation in lymphocyte migration. Long-wavelength three-photon imaging within permissible parameters was able to image the entire LN vasculature in vivo and measure CD8+ T cells and CD4+ T cell motility in the T cell zone over the entire depth of the LN. We observed that the motility of naive CD4+ T cells in the T cell zone during lipopolysaccharide-induced inflammation was dependent on depth. As such, intravital three-photon microscopy had the potential to examine immune cell behavior in the deeper regions of the LN in vivo.
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