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Ultrasound frequency-controlled microbubble dynamics in brain vessels regulate the enrichment of inflammatory pathways in the blood-brain barrier

Author

Listed:
  • Yutong Guo

    (Woodruff School of Mechanical Engineering
    Department of Radiology)

  • Hohyun Lee

    (Woodruff School of Mechanical Engineering)

  • Chulyong Kim

    (Woodruff School of Mechanical Engineering)

  • Christian Park

    (Coulter Department of Biomedical Engineering)

  • Akane Yamamichi

    (Department of Neurological Surgery)

  • Pavlina Chuntova

    (Department of Neurological Surgery)

  • Marco Gallus

    (Department of Neurological Surgery)

  • Miguel O. Bernabeu

    (Usher Institute
    The Bayes Centre)

  • Hideho Okada

    (Department of Neurological Surgery
    Parker Institute for Cancer Immunotherapy)

  • Hanjoong Jo

    (Coulter Department of Biomedical Engineering
    Department of Medicine)

  • Costas Arvanitis

    (Woodruff School of Mechanical Engineering
    Coulter Department of Biomedical Engineering)

Abstract

Microbubble-enhanced ultrasound provides a noninvasive physical method to locally overcome major obstacles to the accumulation of blood-borne therapeutics in the brain, posed by the blood-brain barrier (BBB). However, due to the highly nonlinear and coupled behavior of microbubble dynamics in brain vessels, the impact of microbubble resonant effects on BBB signaling and function remains undefined. Here, combined theoretical and prospective experimental investigations reveal that microbubble resonant effects in brain capillaries can control the enrichment of inflammatory pathways that are sensitive to wall shear stress and promote differential expression of a range of transcripts in the BBB, supporting the notion that microbubble dynamics exerted mechanical stress can be used to establish molecular, in addition to spatial, therapeutic windows to target brain diseases. Consistent with these findings, a robust increase in cytotoxic T-cell accumulation in brain tumors was observed, demonstrating the functional relevance and potential clinical significance of the observed immuno-mechano-biological responses.

Suggested Citation

  • Yutong Guo & Hohyun Lee & Chulyong Kim & Christian Park & Akane Yamamichi & Pavlina Chuntova & Marco Gallus & Miguel O. Bernabeu & Hideho Okada & Hanjoong Jo & Costas Arvanitis, 2024. "Ultrasound frequency-controlled microbubble dynamics in brain vessels regulate the enrichment of inflammatory pathways in the blood-brain barrier," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52329-y
    DOI: 10.1038/s41467-024-52329-y
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    References listed on IDEAS

    as
    1. Michael Vanlandewijck & Liqun He & Maarja Andaloussi Mäe & Johanna Andrae & Koji Ando & Francesca Gaudio & Khayrun Nahar & Thibaud Lebouvier & Bàrbara Laviña & Leonor Gouveia & Ying Sun & Elisabeth Ra, 2018. "Author Correction: A molecular atlas of cell types and zonation in the brain vasculature," Nature, Nature, vol. 560(7716), pages 3-3, August.
    2. Michael Vanlandewijck & Liqun He & Maarja Andaloussi Mäe & Johanna Andrae & Koji Ando & Francesca Del Gaudio & Khayrun Nahar & Thibaud Lebouvier & Bàrbara Laviña & Leonor Gouveia & Ying Sun & Elisabet, 2018. "A molecular atlas of cell types and zonation in the brain vasculature," Nature, Nature, vol. 554(7693), pages 475-480, February.
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