Towards the non-invasive imaging of brain networks and functions at high resolution
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology
Link
https://www.nature.com/articles/s41587-022-01344-9.pdf
Reference5 articles.
1. Xu, H. T., Pan, F., Yang, G. & Gan, W. Choice of cranial window type for in vivo imaging affects dendritic spine turnover in the cortex. Nat. Neurosci. 10, 549–551 (2007). This paper shows that invasive imaging methods such as the use of an open skull window disrupt spine turnover and brain functions.
2. Wang, T. et al. Three-photon imaging of mouse brain structure and function through the intact skull. Nat. Methods 15, 789–792 (2018). This paper demonstrates the great potential of three-photon microscopy for in vivo brain imaging, although image quality is limited by optical aberration and scattering caused by the opaque skull.
3. Hampson, K. M. et al. Adaptive optics for high-resolution imaging. Nat. Rev. Methods Primers 1, 68 (2021). A recent Primer article that summarizes the application of AO for high-resolution optical microscopy.
4. Liu, H. et al. In vivo deep-brain structural and hemodynamic multiphoton microscopy enabled by quantum dots. Nano Lett. 19, 5260–5265 (2019). This paper demonstrates that highly fluorescent quantum dots enable three-photon imaging of the mouse cerebral vasculature up to a depth of 2.1 mm.
5. Papadopoulos, I. N., Jouhanneau, J.-S., Poulet, J. F. A. & Judkewitz, B. Scattering compensation by focus scanning holographic aberration probing (F-SHARP). Nat. Photonics 11, 116–123 (2017). This paper presents a method to measure and correct both optical aberration and scattering of biological tissues for multiphoton microscopy.
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