IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-36083-1.html
   My bibliography  Save this article

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

Author

Listed:
  • Shelei Pan

    (Washington University in St. Louis)

  • Peter H. Yang

    (Washington University in St. Louis)

  • Dakota DeFreitas

    (Washington University in St. Louis)

  • Sruthi Ramagiri

    (Washington University in St. Louis)

  • Peter O. Bayguinov

    (Washington University in St. Louis)

  • Carl D. Hacker

    (Washington University in St. Louis)

  • Abraham Z. Snyder

    (Washington University in St. Louis
    Washington University in St. Louis)

  • Jackson Wilborn

    (Washington University in St. Louis)

  • Hengbo Huang

    (Washington University in St. Louis
    Washington University in St. Louis)

  • Gretchen M. Koller

    (Washington University in St. Louis)

  • Dhvanii K. Raval

    (Washington University in St. Louis)

  • Grace L. Halupnik

    (Washington University in St. Louis)

  • Sanja Sviben

    (Washington University in St. Louis)

  • Samuel Achilefu

    (UT Southwestern Medical Center)

  • Rui Tang

    (Washington University in St. Louis)

  • Gabriel Haller

    (Washington University in St. Louis
    Washington University in St. Louis
    Washington University in St. Louis)

  • James D. Quirk

    (Washington University in St. Louis)

  • James A. J. Fitzpatrick

    (Washington University in St. Louis
    Washington University in St. Louis
    Washington University in St. Louis)

  • Prabagaran Esakky

    (Washington University in St. Louis)

  • Jennifer M. Strahle

    (Washington University in St. Louis
    Washington University in St. Louis
    Washington University in St. Louis)

Abstract

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.

Suggested Citation

  • 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 & Gra, 2023. "Gold nanoparticle-enhanced X-ray microtomography of the rodent reveals region-specific cerebrospinal fluid circulation in the brain," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36083-1
    DOI: 10.1038/s41467-023-36083-1
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-36083-1
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-36083-1?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Eric Song & Alice Gaudin & Amanda R. King & Young-Eun Seo & Hee-Won Suh & Yang Deng & Jiajia Cui & Gregory T. Tietjen & Anita Huttner & W. Mark Saltzman, 2017. "Surface chemistry governs cellular tropism of nanoparticles in the brain," Nature Communications, Nature, vol. 8(1), pages 1-14, August.
    2. Tal Iram & Fabian Kern & Achint Kaur & Saket Myneni & Allison R. Morningstar & Heather Shin & Miguel A. Garcia & Lakshmi Yerra & Robert Palovics & Andrew C. Yang & Oliver Hahn & Nannan Lu & Steven R. , 2022. "Young CSF restores oligodendrogenesis and memory in aged mice via Fgf17," Nature, Nature, vol. 605(7910), pages 509-515, May.
    3. Huixin Xu & Ryann M. Fame & Cameron Sadegh & Jason Sutin & Christopher Naranjo & Syau & Jin Cui & Frederick B. Shipley & Amanda Vernon & Fan Gao & Yong Zhang & Michael J. Holtzman & Myriam Heiman & Be, 2021. "Choroid plexus NKCC1 mediates cerebrospinal fluid clearance during mouse early postnatal development," Nature Communications, Nature, vol. 12(1), pages 1-16, December.
    4. Antoine Louveau & Igor Smirnov & Timothy J. Keyes & Jacob D. Eccles & Sherin J. Rouhani & J. David Peske & Noel C. Derecki & David Castle & James W. Mandell & Kevin S. Lee & Tajie H. Harris & Jonathan, 2015. "Structural and functional features of central nervous system lymphatic vessels," Nature, Nature, vol. 523(7560), pages 337-341, July.
    5. Humberto Mestre & Natasha Verma & Thom D. Greene & LiJing A. Lin & Antonio Ladron-de-Guevara & Amanda M. Sweeney & Guojun Liu & V. Kaye Thomas & Chad A. Galloway & Karen L. Mesy Bentley & Maiken Neder, 2022. "Periarteriolar spaces modulate cerebrospinal fluid transport into brain and demonstrate altered morphology in aging and Alzheimer’s disease," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
    6. Arne Maes & Camille Pestiaux & Alice Marino & Tim Balcaen & Lisa Leyssens & Sarah Vangrunderbeeck & Grzegorz Pyka & Wim M. De Borggraeve & Luc Bertrand & Christophe Beauloye & Sandrine Horman & Martin, 2022. "Cryogenic contrast-enhanced microCT enables nondestructive 3D quantitative histopathology of soft biological tissues," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Laura Bojarskaite & Alexandra Vallet & Daniel M. Bjørnstad & Kristin M. Gullestad Binder & Céline Cunen & Kjell Heuser & Miroslav Kuchta & Kent-Andre Mardal & Rune Enger, 2023. "Sleep cycle-dependent vascular dynamics in male mice and the predicted effects on perivascular cerebrospinal fluid flow and solute transport," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    2. Carolin Beuker & David Schafflick & Jan-Kolja Strecker & Michael Heming & Xiaolin Li & Jolien Wolbert & Antje Schmidt-Pogoda & Christian Thomas & Tanja Kuhlmann & Irene Aranda-Pardos & Noelia A-Gonzal, 2022. "Stroke induces disease-specific myeloid cells in the brain parenchyma and pia," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    3. Miao Wang & Congcong Yan & Xi Li & Tianhao Yang & Shengnan Wu & Qian Liu & Qingming Luo & Feifan Zhou, 2024. "Non-invasive modulation of meningeal lymphatics ameliorates ageing and Alzheimer’s disease-associated pathology and cognition in mice," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    4. Geir Ringstad & Per Kristian Eide, 2023. "The pitfalls of interpreting hyperintense FLAIR signal as lymph outside the human brain," Nature Communications, Nature, vol. 14(1), pages 1-3, December.
    5. Dongyu Li & Shaojun Liu & Tingting Yu & Zhang Liu & Silin Sun & Denis Bragin & Alexander Shirokov & Nikita Navolokin & Olga Bragina & Zhengwu Hu & Jürgen Kurths & Ivan Fedosov & Inna Blokhina & Alexan, 2023. "Photostimulation of brain lymphatics in male newborn and adult rodents for therapy of intraventricular hemorrhage," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    6. Weiping Dai & Mengqian Yang & Pei Xia & Chuan Xiao & Shuying Huang & Zhan Zhang & Xin Cheng & Wenchang Li & Jian Jin & Jingyun Zhang & Binghuo Wu & Yingying Zhang & Pei-hui Wu & Yangyang Lin & Wen Wu , 2022. "A functional role of meningeal lymphatics in sex difference of stress susceptibility in mice," Nature Communications, Nature, vol. 13(1), pages 1-21, December.
    7. Per Kristian Eide & Geir Ringstad, 2024. "Functional analysis of the human perivascular subarachnoid space," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    8. Yogi H. Hendlin, 2022. "Plant Philosophy and Interpretation: Making Sense of Contemporary Plant Intelligence Debates," Environmental Values, , vol. 31(3), pages 253-276, June.
    9. Per Kristian Eide & Aslan Lashkarivand & Are Pripp & Lars Magnus Valnes & Markus Herberg Hovd & Geir Ringstad & Kaj Blennow & Henrik Zetterberg, 2023. "Plasma neurodegeneration biomarker concentrations associate with glymphatic and meningeal lymphatic measures in neurological disorders," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    10. Nicola A. Kearns & Artemis Iatrou & Daniel J. Flood & Sashini Tissera & Zachary M. Mullaney & Jishu Xu & Chris Gaiteri & David A. Bennett & Yanling Wang, 2023. "Dissecting the human leptomeninges at single-cell resolution," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    11. Hadi Abou-El-Hassan & Rafael M. Rezende & Saef Izzy & Galina Gabriely & Taha Yahya & Bruna K. Tatematsu & Karl J. Habashy & Juliana R. Lopes & Gislane L. V. Oliveira & Amir-Hadi Maghzi & Zhuoran Yin &, 2023. "Vγ1 and Vγ4 gamma-delta T cells play opposing roles in the immunopathology of traumatic brain injury in males," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    12. Josephine A. Mapunda & Javier Pareja & Mykhailo Vladymyrov & Elisa Bouillet & Pauline Hélie & Petr Pleskač & Sara Barcos & Johanna Andrae & Dietmar Vestweber & Donald M. McDonald & Christer Betsholtz , 2023. "VE-cadherin in arachnoid and pia mater cells serves as a suitable landmark for in vivo imaging of CNS immune surveillance and inflammation," Nature Communications, Nature, vol. 14(1), pages 1-23, December.
    13. Anastasia Mozokhina & Rostislav Savinkov, 2020. "Mathematical Modelling of the Structure and Function of the Lymphatic System," Mathematics, MDPI, vol. 8(9), pages 1-18, September.
    14. Shinji Naganawa & Yutaka Kato & Tadao Yoshida & Michihiko Sone, 2023. "Fluid signal suppression characteristics of 3D-FLAIR with a T2 selective inversion pulse in the skull base," Nature Communications, Nature, vol. 14(1), pages 1-3, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36083-1. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.