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Critical data-based re-evaluation of minocycline as a putative specific microglia inhibitor.
Möller, Thomas; Bard, Frédérique; Bhattacharya, Anindya; Biber, Knut; Campbell, Brian; Dale, Elena; Eder, Claudia; Gan, Li; Garden, Gwenn A; Hughes, Zoë A; Pearse, Damien D; Staal, Roland G W; Sayed, Faten A; Wes, Paul D; Boddeke, Hendrikus W G M.
Afiliación
  • Möller T; Neuroinflammation Disease Biology Unit, Lundbeck Research USA, Paramus, New Jersey.
  • Bard F; Department of Neurology, University of Washington, Seattle, Washington.
  • Bhattacharya A; Janssen Prevention Center, San Diego, California.
  • Biber K; Janssen Research & Development, LLC., Neuroscience Drug Discovery, San Diego, California.
  • Campbell B; Department of Psychiatry and Psychotherapy, University Hospital Freiburg, Freiburg, Germany.
  • Dale E; Department of Neuroscience, University Medical Center Groningen, Groningen, The Netherlands.
  • Eder C; Neuroinflammation Disease Biology Unit, Lundbeck Research USA, Paramus, New Jersey.
  • Gan L; Neuroinflammation Disease Biology Unit, Lundbeck Research USA, Paramus, New Jersey.
  • Garden GA; Institute for Infection and Immunity, St. George's - University of London, London, United Kingdom.
  • Hughes ZA; Gladstone Institute for Neurodegeneration, San Francisco, California.
  • Pearse DD; Department of Neurology, University of Washington, Seattle, Washington.
  • Staal RG; Neuroscience & Pain Research Unit, Pfizer Global Research, Cambridge, Massachusetts.
  • Sayed FA; Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida.
  • Wes PD; Neuroinflammation Disease Biology Unit, Lundbeck Research USA, Paramus, New Jersey.
  • Boddeke HW; Gladstone Institute for Neurodegeneration, San Francisco, California.
Glia ; 64(10): 1788-94, 2016 10.
Article en En | MEDLINE | ID: mdl-27246804
ABSTRACT
Minocycline, a second generation broad-spectrum antibiotic, has been frequently postulated to be a "microglia inhibitor." A considerable number of publications have used minocycline as a tool and concluded, after achieving a pharmacological effect, that the effect must be due to "inhibition" of microglia. It is, however, unclear how this "inhibition" is achieved at the molecular and cellular levels. Here, we weigh the evidence whether minocycline is indeed a bona fide microglia inhibitor and discuss how data generated with minocycline should be interpreted. GLIA 2016;641788-1794.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Microglía / Minociclina / Antibacterianos Límite: Animals / Humans Idioma: En Revista: Glia Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Microglía / Minociclina / Antibacterianos Límite: Animals / Humans Idioma: En Revista: Glia Asunto de la revista: NEUROLOGIA Año: 2016 Tipo del documento: Article