Age-related alterations in meningeal immunity drive impaired CNS lymphatic drainage

Author:

Rustenhoven Justin1234ORCID,Pavlou Georgios5ORCID,Storck Steffen E.12ORCID,Dykstra Taitea12ORCID,Du Siling126ORCID,Wan Zhengpeng5ORCID,Quintero Daniel12ORCID,Scallan Joshua P.7ORCID,Smirnov Igor12ORCID,Kamm Roger D.58ORCID,Kipnis Jonathan126ORCID

Affiliation:

1. Brain Immunology and Glia Center, School of Medicine, Washington University in St. Louis 1 , St. Louis, MO, USA

2. School of Medicine, Washington University in St. Louis 2 Department of Pathology and Immunology, , St. Louis, MO, USA

3. The University of Auckland 3 Department of Pharmacology and Clinical Pharmacology, , Auckland, New Zealand

4. Centre for Brain Research, The University of Auckland 4 , Auckland, New Zealand

5. Massachusetts Institute of Technology 5 Department of Biological Engineering, , Cambridge, MA, USA

6. Immunology Graduate Program, School of Medicine, Washington University in St. Louis 6 , St. Louis, MO, USA

7. University of South Florida 7 Department of Molecular Pharmacology and Physiology, , Tampa, FL, USA

8. Massachusetts Institute of Technology 8 Department of Mechanical Engineering, , Cambridge, MA, USA

Abstract

The meningeal lymphatic network enables the drainage of cerebrospinal fluid (CSF) and facilitates the removal of central nervous system (CNS) waste. During aging and in Alzheimer’s disease, impaired meningeal lymphatic drainage promotes the buildup of toxic misfolded proteins in the CNS. Reversing this age-related dysfunction represents a promising strategy to augment CNS waste clearance; however, the mechanisms underlying this decline remain elusive. Here, we demonstrate that age-related alterations in meningeal immunity underlie this lymphatic impairment. Single-cell RNA sequencing of meningeal lymphatic endothelial cells from aged mice revealed their response to IFNγ, which was increased in the aged meninges due to T cell accumulation. Chronic elevation of meningeal IFNγ in young mice via AAV-mediated overexpression attenuated CSF drainage—comparable to the deficits observed in aged mice. Therapeutically, IFNγ neutralization alleviated age-related impairments in meningeal lymphatic function. These data suggest manipulation of meningeal immunity as a viable approach to normalize CSF drainage and alleviate the neurological deficits associated with impaired waste removal.

Funder

National Institutes of Health

Royal Society of New Zealand Te Apārangi

Cure Alzheimer’s Fund

Ludwig Family Foundation

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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