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Age-related alterations in meningeal immunity drive impaired CNS lymphatic drainage.
Rustenhoven, Justin; Pavlou, Georgios; Storck, Steffen E; Dykstra, Taitea; Du, Siling; Wan, Zhengpeng; Quintero, Daniel; Scallan, Joshua P; Smirnov, Igor; Kamm, Roger D; Kipnis, Jonathan.
Afiliação
  • Rustenhoven J; Brain Immunology and Glia Center, School of Medicine, Washington University in St. Louis , St. Louis, MO, USA.
  • Pavlou G; Department of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
  • Storck SE; Department of Pharmacology and Clinical Pharmacology, The University of Auckland, Auckland, New Zealand.
  • Dykstra T; Centre for Brain Research, The University of Auckland , Auckland, New Zealand.
  • Du S; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Wan Z; Brain Immunology and Glia Center, School of Medicine, Washington University in St. Louis , St. Louis, MO, USA.
  • Quintero D; Department of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
  • Scallan JP; Brain Immunology and Glia Center, School of Medicine, Washington University in St. Louis , St. Louis, MO, USA.
  • Smirnov I; Department of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
  • Kamm RD; Brain Immunology and Glia Center, School of Medicine, Washington University in St. Louis , St. Louis, MO, USA.
  • Kipnis J; Department of Pathology and Immunology, School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
J Exp Med ; 220(7)2023 07 03.
Article em En | MEDLINE | ID: mdl-37027179
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vasos Linfáticos / Doença de Alzheimer Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vasos Linfáticos / Doença de Alzheimer Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article