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Characterization of the responses of brain macrophages to focused ultrasound-mediated blood-brain barrier opening.
Kline-Schoder, Alina R; Chintamen, Sana; Willner, Moshe J; DiBenedetto, Melody R; Noel, Rebecca L; Batts, Alec J; Kwon, Nancy; Zacharoulis, Stergios; Wu, Cheng-Chia; Menon, Vilas; Kernie, Steven G; Konofagou, Elisa E.
Afiliación
  • Kline-Schoder AR; Department of Biomedical Engineering, Columbia University, New York, NY, USA.
  • Chintamen S; Department of Neurobiology and Behaviour, Columbia University, New York, NY, USA.
  • Willner MJ; Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA.
  • DiBenedetto MR; Department of Biomedical Engineering, Columbia University, New York, NY, USA.
  • Noel RL; Department of Biomedical Engineering, Columbia University, New York, NY, USA.
  • Batts AJ; Department of Biomedical Engineering, Columbia University, New York, NY, USA.
  • Kwon N; Department of Biomedical Engineering, Columbia University, New York, NY, USA.
  • Zacharoulis S; Department of Pediatrics, Columbia University, New York, NY, USA.
  • Wu CC; Department of Pediatrics, Columbia University, New York, NY, USA.
  • Menon V; Department of Neurology, Columbia University, New York, NY, USA.
  • Kernie SG; Department of Pediatrics, Columbia University, New York, NY, USA.
  • Konofagou EE; Department of Biomedical Engineering, Columbia University, New York, NY, USA. ek2191@columbia.edu.
Nat Biomed Eng ; 8(5): 650-663, 2024 May.
Article en En | MEDLINE | ID: mdl-37857722
The opening of the blood-brain barrier (BBB) by focused ultrasound (FUS) coupled with intravenously injected microbubbles can be leveraged as a form of immunotherapy for the treatment of neurodegenerative disorders. However, how FUS BBB opening affects brain macrophages is not well understood. Here by using single-cell sequencing to characterize the distinct responses of microglia and central nervous system-associated macrophages (CAMs) to FUS-mediated BBB opening in mice, we show that the treatment remodels the immune landscape via the recruitment of CAMs and the proliferation of microglia and via population size increases in disease-associated microglia. Both microglia and CAMs showed early and late increases in population sizes, yet only the proliferation of microglia increased at both timepoints. The population of disease-associated microglia also increased, accompanied by the upregulation of genes associated with gliogenesis and phagocytosis, with the depletion of brain macrophages significantly decreasing the duration of BBB opening.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Asunto principal: Encéfalo / Barrera Hematoencefálica / Microglía / Macrófagos Límite: Animals Idioma: En Revista: Nat biomed eng Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Encéfalo / Barrera Hematoencefálica / Microglía / Macrófagos Límite: Animals Idioma: En Revista: Nat biomed eng Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos