Randomized trial demonstrates enhanced imaging stability in mouse models, suggesting improved visualization of biological processes.
Recent advances in computational microscopy enable highspeed high-resolution intravital 3D imaging with low phototoxicity. However, inevitable sample vibration and tissue deformation in multi-cellular organisms make it extremely challenging to maintain samples stably in focus over long-term even with an extended effective depth of field. Here, we propose a real-time robust autofocus method based on scanning light-field microscopy (AFsLF), enabling sustained high-speed 3D imaging of diverse samples across several days by continuously tracking the sample focal plane without hardware modifications. Based on the intrinsic disparity of light-field angular measurements, AFsLF estimates the focal plane with less than 2 µm error over a 500 µm depth range, completing within 0.1 s, 300-time faster than previous methods. We validate AFsLF across diverse tissues and challenging conditions, including low excitation power, multichannel illumination, and large axial displacements, enabling stable, long-term, multichannel subcellular imaging of neural activities and immune responses in mouse brain and liver. Continuous focus maintenance during intravital 3D imaging remains challenging. Here, Wang et al. proposed a real-time autofocus method for scanning light-field microscopy that enables stable, long-term, multichannel subcellular imaging of neural activities and immune responses in mouse brain and liver.
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Wang et al. (2026) studied this question.
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