Gold nanoparticle-enhanced X-ray microtomography of the rodent reveals region-specific cerebrospinal fluid circulation in the brain

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作者
Shelei Pan
Peter H. Yang
Dakota DeFreitas
Sruthi Ramagiri
Peter O. Bayguinov
Carl D. Hacker
Abraham Z. Snyder
Jackson Wilborn
Hengbo Huang
Gretchen M. Koller
Dhvanii K. Raval
Grace L. Halupnik
Sanja Sviben
Samuel Achilefu
Rui Tang
Gabriel Haller
James D. Quirk
James A. J. Fitzpatrick
Prabagaran Esakky
Jennifer M. Strahle
机构
[1] Washington University in St. Louis,Department of Neurosurgery, Washington University School of Medicine
[2] Washington University in St. Louis,Washington University Center for Cellular Imaging, Washington University School of Medicine
[3] Washington University in St. Louis,Department of Radiology, Washington University School of Medicine
[4] Washington University in St. Louis,Department of Neurology, Washington University School of Medicine
[5] Washington University in St. Louis,Department of Biomedical Engineering
[6] UT Southwestern Medical Center,Department of Biomedical Engineering
[7] Washington University in St. Louis,Department of Genetics, Washington University School of Medicine
[8] Washington University in St. Louis,Department of Neuroscience, Washington University School of Medicine
[9] Washington University in St. Louis,Department of Cell Biology and Physiology, Washington University School of Medicine
[10] Washington University in St. Louis,Department of Orthopedic Surgery, Washington University School of Medicine
[11] Washington University in St. Louis,Department of Pediatrics, Washington University School of Medicine
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摘要
Cerebrospinal fluid (CSF) is essential for the development and function of the central nervous system (CNS). However, the brain and its interstitium have largely been thought of as a single entity through which CSF circulates, and it is not known whether specific cell populations within the CNS preferentially interact with the CSF. Here, we develop a technique for CSF tracking, gold nanoparticle-enhanced X-ray microtomography, to achieve micrometer-scale resolution visualization of CSF circulation patterns during development. Using this method and subsequent histological analysis in rodents, we identify previously uncharacterized CSF pathways from the subarachnoid space (particularly the basal cisterns) that mediate CSF-parenchymal interactions involving 24 functional-anatomic cell groupings in the brain and spinal cord. CSF distribution to these areas is largely restricted to early development and is altered in posthemorrhagic hydrocephalus. Our study also presents particle size-dependent CSF circulation patterns through the CNS including interaction between neurons and small CSF tracers, but not large CSF tracers. These findings have implications for understanding the biological basis of normal brain development and the pathogenesis of a broad range of disease states, including hydrocephalus.
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