TY - JOUR
T1 - Should We Stop Saying ‘Glia’ and ‘Neuroinflammation’?
AU - Masgrau, Roser
AU - Guaza, Carmen
AU - Ransohoff, Richard M.
AU - Galea, Elena
PY - 2017/6/1
Y1 - 2017/6/1
N2 - © 2017 Elsevier Ltd 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.
AB - © 2017 Elsevier Ltd 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.
KW - cell replacement
KW - central nervous system circuits
KW - central nervous system repair
KW - computation
KW - induced pluripotent stem cell
KW - single-cell RNA sequencing
U2 - 10.1016/j.molmed.2017.04.005
DO - 10.1016/j.molmed.2017.04.005
M3 - Review article
SN - 1471-4914
VL - 23
SP - 486
EP - 500
JO - Trends in Molecular Medicine
JF - Trends in Molecular Medicine
IS - 6
ER -