4.8 Article

Meningeal lymphatic dysfunction exacerbates traumatic brain injury pathogenesis

Journal

NATURE COMMUNICATIONS
Volume 11, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41467-020-18113-4

Keywords

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Funding

  1. National Institutes of Health/National Institute of Neurological Disorders and Stroke [R01NS106383]
  2. Alzheimer's Association [AARG-18-566113]
  3. Owens Family Foundation
  4. University of Virginia Research and Development Award
  5. Wagner Fellowship
  6. Biomedical Data Sciences Training Grant [T32LM012416]
  7. Cell and Molecular Biology Training Grant [T32GM008136]
  8. R35 grant [5R35GM128635-02]
  9. NIH National Institute of General Medical Sciences predoctoral training grant [3T32GM008328]
  10. National Multiple Sclerosis Foundation Postdoctoral Fellowship [FG-1707-28590]
  11. Medical Scientist Training Program Grant [5T32GM007267-38]
  12. Immunology Training Grant [5T32AI007496-25]

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Traumatic brain injury (TBI) is a leading global cause of death and disability. Here we demonstrate in an experimental mouse model of TBI that mild forms of brain trauma cause severe deficits in meningeal lymphatic drainage that begin within hours and last out to at least one month post-injury. To investigate a mechanism underlying impaired lymphatic function in TBI, we examined how increased intracranial pressure (ICP) influences the meningeal lymphatics. We demonstrate that increased ICP can contribute to meningeal lymphatic dysfunction. Moreover, we show that pre-existing lymphatic dysfunction before TBI leads to increased neuroinflammation and negative cognitive outcomes. Finally, we report that rejuvenation of meningeal lymphatic drainage function in aged mice can ameliorate TBI-induced gliosis. These findings provide insights into both the causes and consequences of meningeal lymphatic dysfunction in TBI and suggest that therapeutics targeting the meningeal lymphatic system may offer strategies to treat TBI.

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