4.6 Review

Should We Stop Saying 'Glia' and 'Neuroinflammation'?

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 23, Issue 6, Pages 486-500

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2017.04.005

Keywords

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Funding

  1. Ministerio de Economia y Competitividad, Spain [BFU2012-38844, BFU2016-79735-P]
  2. Autonomous Government of Catalonia AGAUR [2014SGR98]
  3. European Leukodystrophy Foundation
  4. Catalonian Marato-TV3 Foundation
  5. Ministerio de Economia y Competitividad [SAF2013-42784-R]
  6. Red Espanola de Esclerosis Multiple (REEM) - Fondo de Investigacion Sanitaria (FIS) [RD12/0032/0008]
  7. ICREA Funding Source: Custom

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Central nervous system (CNS) therapeutics based on the theoretical framework of neuroinflammation have only barely succeeded. We argue that a problem may be the wrong use of the term 'neuroinflammation' as a distinct nosological entity when, based on recent evidence, it may not explain CNS disease pathology. Indeed, the terms 'neuroinflammation' and 'glia' could be obsolete. First, unbiased molecular profiling of CNS cell populations and individual cells reveals striking phenotypic heterogeneity in health and disease. Second, astrocytes, microglia, oligodendrocytes, and NG2 cells may contribute to higher-brain functions by performing actions beyond housekeeping. We propose that CNS diseases be viewed as failed circuits caused in part by disease-specific dysfunction of cells traditionally called 'glia', and hence, favor therapies promoting their functional recovery.

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