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| Format: | Preprint |
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2024
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| Online-Zugang: | https://arxiv.org/abs/2404.11901 |
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| author | Liu, Kunzan Cao, Honghao Shashaty, Kasey Yu, Li-Yu Spitz, Sarah Pramotton, Francesca Michela Wan, Zhengpeng Kan, Ellen L. Tevonian, Erin N. Levy, Manuel Lendaro, Eva Kamm, Roger D. Griffith, Linda G. Wang, Fan Qiu, Tong You, Sixian |
| author_facet | Liu, Kunzan Cao, Honghao Shashaty, Kasey Yu, Li-Yu Spitz, Sarah Pramotton, Francesca Michela Wan, Zhengpeng Kan, Ellen L. Tevonian, Erin N. Levy, Manuel Lendaro, Eva Kamm, Roger D. Griffith, Linda G. Wang, Fan Qiu, Tong You, Sixian |
| contents | Label-free imaging through two-photon autofluorescence (2PAF) of NAD(P)H allows for non-destructive and high-resolution visualization of cellular activities in living systems. However, its application to thick tissues and organoids has been restricted by its limited penetration depth within 300 $μ$m, largely due to tissue scattering at the typical excitation wavelength (~750 nm) required for NAD(P)H. Here, we demonstrate that the imaging depth for NAD(P)H can be extended to over 700 $μ$m in living engineered human multicellular microtissues by adopting multimode fiber (MMF)-based low-repetition-rate high-peak-power three-photon (3P) excitation of NAD(P)H at 1100 nm. This is achieved by having over 0.5 MW peak power at the band of 1100$\pm$25 nm through adaptively modulating multimodal nonlinear pulse propagation with a compact fiber shaper. Moreover, the 8-fold increase in pulse energy at 1100 nm enables faster imaging of monocyte behaviors in the living multicellular models. These results represent a significant advance for deep and dynamic metabolic and structural imaging of intact living biosystems. The modular design (MMF with a slip-on fiber shaper) is anticipated to allow wide adoption of this methodology for demanding in vivo and in vitro imaging applications, including cancer research, autoimmune diseases, and tissue engineering. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2404_11901 |
| institution | arXiv |
| publishDate | 2024 |
| record_format | arxiv |
| spellingShingle | Deep and Dynamic Metabolic and Structural Imaging in Living Tissues Liu, Kunzan Cao, Honghao Shashaty, Kasey Yu, Li-Yu Spitz, Sarah Pramotton, Francesca Michela Wan, Zhengpeng Kan, Ellen L. Tevonian, Erin N. Levy, Manuel Lendaro, Eva Kamm, Roger D. Griffith, Linda G. Wang, Fan Qiu, Tong You, Sixian Optics Biological Physics Label-free imaging through two-photon autofluorescence (2PAF) of NAD(P)H allows for non-destructive and high-resolution visualization of cellular activities in living systems. However, its application to thick tissues and organoids has been restricted by its limited penetration depth within 300 $μ$m, largely due to tissue scattering at the typical excitation wavelength (~750 nm) required for NAD(P)H. Here, we demonstrate that the imaging depth for NAD(P)H can be extended to over 700 $μ$m in living engineered human multicellular microtissues by adopting multimode fiber (MMF)-based low-repetition-rate high-peak-power three-photon (3P) excitation of NAD(P)H at 1100 nm. This is achieved by having over 0.5 MW peak power at the band of 1100$\pm$25 nm through adaptively modulating multimodal nonlinear pulse propagation with a compact fiber shaper. Moreover, the 8-fold increase in pulse energy at 1100 nm enables faster imaging of monocyte behaviors in the living multicellular models. These results represent a significant advance for deep and dynamic metabolic and structural imaging of intact living biosystems. The modular design (MMF with a slip-on fiber shaper) is anticipated to allow wide adoption of this methodology for demanding in vivo and in vitro imaging applications, including cancer research, autoimmune diseases, and tissue engineering. |
| title | Deep and Dynamic Metabolic and Structural Imaging in Living Tissues |
| topic | Optics Biological Physics |
| url | https://arxiv.org/abs/2404.11901 |