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CNS tau efflux via exosomes is likely increased in Parkinson's disease but not in Alzheimer's disease.
Shi, Min; Kovac, Andrej; Korff, Ane; Cook, Travis J; Ginghina, Carmen; Bullock, Kristin M; Yang, Li; Stewart, Tessandra; Zheng, Danfeng; Aro, Patrick; Atik, Anzari; Kerr, Kathleen F; Zabetian, Cyrus P; Peskind, Elaine R; Hu, Shu-Ching; Quinn, Joseph F; Galasko, Douglas R; Montine, Thomas J; Banks, William A; Zhang, Jing.
Afiliación
  • Shi M; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Kovac A; Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Division of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA; Institute of Neuroimmunology, Slovak Academy o
  • Korff A; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Cook TJ; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Ginghina C; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Bullock KM; Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Division of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.
  • Yang L; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Stewart T; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Zheng D; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA; Department of Pathology, Peking University Health Science Center and Peking University Third Hospital, Beijing, China.
  • Aro P; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Atik A; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Kerr KF; Department of Biostatistics, University of Washington, Seattle, WA, USA.
  • Zabetian CP; Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Parkinson's Disease Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Department of Neurology, University of Washington Sc
  • Peskind ER; Department of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, WA, USA; Mental Illness Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA.
  • Hu SC; Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Parkinson's Disease Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Department of Neurology, University of Washington Sc
  • Quinn JF; Department of Neurology, Oregon Health and Science University, Portland, OR, USA.
  • Galasko DR; Department of Neurosciences and Shiley-Marcos Alzheimer's Disease Research Center, University of California at San Diego, La Jolla, CA, USA.
  • Montine TJ; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA.
  • Banks WA; Geriatric Research, Education, and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA, USA; Division of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.
  • Zhang J; Department of Pathology, University of Washington School of Medicine, Seattle, WA, USA; Department of Pathology, Peking University Health Science Center and Peking University Third Hospital, Beijing, China. Electronic address: zhangj@uw.edu.
Alzheimers Dement ; 12(11): 1125-1131, 2016 11.
Article en En | MEDLINE | ID: mdl-27234211
INTRODUCTION: Alzheimer's disease (AD) and Parkinson's disease (PD) involve tau pathology. Tau is detectable in blood, but its clearance from neuronal cells and the brain is poorly understood. METHODS: Tau efflux from the brain to the blood was evaluated by administering radioactively labeled and unlabeled tau intracerebroventricularly in wild-type and tau knock-out mice, respectively. Central nervous system (CNS)-derived tau in L1CAM-containing exosomes was further characterized extensively in human plasma, including by single molecule array technology with 303 subjects. RESULTS: The efflux of Tau, including a fraction via CNS-derived L1CAM exosomes, was observed in mice. In human plasma, tau was explicitly identified within L1CAM exosomes. In contrast to AD patients, L1CAM exosomal tau was significantly higher in PD patients than controls and correlated with cerebrospinal fluid tau. CONCLUSIONS: Tau is readily transported from the brain to the blood. The mechanisms of CNS tau efflux are likely different between AD and PD.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas tau / Exosomas / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Adult / Aged / Aged80 / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Proteínas tau / Exosomas / Enfermedad de Alzheimer Tipo de estudio: Prognostic_studies Límite: Adult / Aged / Aged80 / Animals / Female / Humans / Male / Middle aged Idioma: En Revista: Alzheimers Dement Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos