An optical clearing imaging window: Realization of mouse brain imaging and manipulation through scalp and skull.

Cortical visualization is essential to understand the dynamic changes in brain microenvironment under physiopathological conditions. However, the turbid scalp and skull severely limit the imaging depth and resolution. Existing cranial windows require invasive scalp excision and various subsequent skull treatments. Non-invasive in vivo imaging of skull bone marrow, meninges, and cortex through scalp and skull with high resolution yet remains a challenge. In this work, a non-invasive trans-scalp/skull optical clearing imaging window is proposed for cortical and calvarial imaging, which is achieved by applying a novel skin optical clearing reagent. The imaging depth and resolution are greatly enhanced in near infrared imaging and optical coherence tomography imaging. Combining this imaging window with adaptive optics, we achieve the visualization and manipulation of the calvarial and cortical microenvironment through the scalp and skull using two-photon imaging for the first time. Our method provides a well-performed imaging window and paves the way for intravital brain studies with the advantages of easy-operation, convenience and non-invasiveness.

[1]  Lihong V. Wang,et al.  Optical-resolution photoacoustic microscopy with a needle-shaped beam , 2022, Nature Photonics.

[2]  Tingting Yu,et al.  A Through-Intact-Skull (TIS) chronic window technique for cortical structure and function observation in mice , 2022, eLight.

[3]  Chao Zhang,et al.  A Long‐Term Clearing Cranial Window for Longitudinal Imaging of Cortical and Calvarial Ischemic Injury through the Intact Skull , 2022, Advanced science.

[4]  Menglei Zha,et al.  Promoted NIR-II Fluorescence by Heteroatom-Inserted Rigid-Planar Cores for Monitoring Cell Therapy of Acute Lung Injury. , 2021, Small.

[5]  Chao Zhang,et al.  Assessment of tissue‐specific changes in structure and function induced by in vivo skin/skull optical clearing techniques , 2021, Lasers in surgery and medicine.

[6]  R. Calabró,et al.  Can Cranioplasty Be Considered a Tool to Improve Cognitive Recovery Following Traumatic Brain Injury? A 5-Years Retrospective Study , 2021, Journal of clinical medicine.

[7]  Maxim N. Artyomov,et al.  Heterogeneity of meningeal B cells reveals a lymphopoietic niche at the CNS borders , 2021, Science.

[8]  Jasmin Herz,et al.  Skull and vertebral bone marrow are myeloid cell reservoirs for the meninges and CNS parenchyma , 2021, Science.

[9]  Tingting Yu,et al.  Physical and chemical mechanisms of tissue optical clearing , 2021, iScience.

[10]  Yong He,et al.  Non-invasive, opsin-free mid-infrared modulation activates cortical neurons and accelerates associative learning , 2020, Nature Communications.

[11]  T. Nemoto,et al.  PEO-CYTOP Fluoropolymer Nanosheets as a Novel Open-Skull Window for Imaging of the Living Mouse Brain , 2020, iScience.

[12]  B. Tang,et al.  Visible‐near infrared‐II skull optical clearing window for in vivo cortical vasculature imaging and targeted manipulation , 2020, Journal of biophotonics.

[13]  Defu Chen,et al.  Penetration-enhanced optical coherence tomography angiography with optical clearing agent for clinical evaluation of human skin. , 2020, Photodiagnosis and photodynamic therapy.

[14]  V. Tuchin,et al.  The Optical Clearing Method , 2019, SpringerBriefs in Physics.

[15]  Markus Rempfler,et al.  Panoptic imaging of transparent mice reveals whole-body neuronal projections and skull-meninges connections , 2018, Nature Neuroscience.

[16]  A. Chenn,et al.  Leukaemia hijacks a neural mechanism to invade the central nervous system , 2018, Nature.

[17]  Q. Luo,et al.  A large, switchable optical clearing skull window for cerebrovascular imaging , 2018, Theranostics.

[18]  Dan Zhu,et al.  Skull optical clearing window for in vivo imaging of the mouse cortex at synaptic resolution , 2017, Light: Science & Applications.

[19]  Dan Zhu,et al.  A useful way to develop effective in vivo skin optical clearing agents , 2017, Journal of biophotonics.

[20]  Zhihong Zhang,et al.  FSOCA‐induced switchable footpad skin optical clearing window for blood flow and cell imaging in vivo , 2017, Journal of biophotonics.

[21]  Na Ji Adaptive optical fluorescence microscopy , 2017, Nature Methods.

[22]  Mark J. Schnitzer,et al.  Impermanence of dendritic spines in live adult CA1 hippocampus , 2015, Nature.

[23]  T. Jones,et al.  Chronic Monitoring of Vascular Progression after Ischemic Stroke Using Multiexposure Speckle Imaging and Two-Photon Fluorescence Microscopy , 2015, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[24]  Deborah S. Barkauskas,et al.  Comparison of intravital thinned skull and cranial window approaches to study CNS immunobiology in the mouse cortex , 2014, Intravital.

[25]  Qingming Luo,et al.  Recent progress in tissue optical clearing , 2013, Laser & photonics reviews.

[26]  Dan Zhu,et al.  An innovative transparent cranial window based on skull optical clearing , 2012 .

[27]  Christopher G. Rylander,et al.  Erratum: Mechanical tissue optical clearing technique increases imaging resolution and contrast through Ex vivo porcine skin , 2011 .

[28]  Qingming Luo,et al.  Quantitative analysis of dehydration in porcine skin for assessing mechanism of optical clearing. , 2011, Journal of biomedical optics.

[29]  D. Kleinfeld,et al.  Chronic optical access through a polished and reinforced thinned skull , 2010 .

[30]  Alvin T Yeh,et al.  Molecular basis for optical clearing of collagenous tissues. , 2010, Journal of biomedical optics.

[31]  Jaime Grutzendler,et al.  Thinned-skull cranial window technique for long-term imaging of the cortex in live mice , 2010, Nature Protocols.

[32]  J. Dwek The periosteum: what is it, where is it, and what mimics it in its absence? , 2010, Skeletal Radiology.

[33]  M. Levene,et al.  Microprisms for in vivo multilayer cortical imaging. , 2009, Journal of neurophysiology.

[34]  K. Svoboda,et al.  Long-term, high-resolution imaging in the mouse neocortex through a chronic cranial window , 2009, Nature Protocols.

[35]  W. Gan,et al.  Choice of cranial window type for in vivo imaging affects dendritic spine turnover in the cortex , 2007, Nature Neuroscience.

[36]  K. Svoboda,et al.  Principles of Two-Photon Excitation Microscopy and Its Applications to Neuroscience , 2006, Neuron.

[37]  W. Denk,et al.  Deep tissue two-photon microscopy , 2005, Nature Methods.

[38]  A. Gefen,et al.  Age-dependent changes in material properties of the brain and braincase of the rat. , 2003, Journal of neurotrauma.

[39]  R Paus,et al.  A comprehensive guide for the accurate classification of murine hair follicles in distinct hair cycle stages. , 2001, The Journal of investigative dermatology.

[40]  S. Eichmüller,et al.  Generation and cyclic remodeling of the hair follicle immune system in mice. , 1998, The Journal of investigative dermatology.

[41]  J E Coggle,et al.  The influence of the hair cycle on the thickness of mouse skin , 1984, The Anatomical record.