NG2 cells are not a major source of reactive astrocytes after neocortical stab wound injury

Mila Komitova, David R. Serwanski, Q. Richard Lu, Akiko Nishiyama

Research output: Contribution to journalArticlepeer-review

72 Scopus citations


NG2 cells are an abundant glial cell type in the adult brain. They are distinct from astrocytes, mature oligodendrocytes, and microglia. NG2 cells generate oligodendrocytes and a subpopulation of protoplasmic astrocytes in the ventral forebrain during development. To determine whether NG2 cells generate reactive astrocytes in the lesioned brain, stab wound injury was created in adult NG2creBAC:ZEG double transgenic mice, in which enhanced green fluorescent protein (EGFP) is expressed in NG2 cells and their progeny, and the phenotype of the EGFP+ cells was analyzed at 10 and 30 days post lesion (dpl). The majority (>90%) of the reactive astrocytes surrounding the lesion that expressed glial fibrillary acidic protein (GFAP) lacked EGFP expression, and conversely the majority (>90%) of EGFP+ cells were GFAP-negative. However, 8% of EGFP+ cells co-expressed GFAP at 10 dpl. Most of these EGFP+GFAP+ cells were morphologically distinct from hypertrophic reactive astrocytes and exhibited weak GFAP expression. NG2 was detected in a fraction of the EGFP+GFAP+ cells found at 10 dpl. By 30 dpl the number of EGFP+GFAP+ cells had decreased more than four-fold from 10 dpl. A similar transient appearance of EGFP+GFAP+ cells with simple morphology was observed in NG2creER™:ZEG double transgenic mice in which EGFP expression had been induced in NG2 cells prior to injury. NG2 cell-specific deletion of the oligodendrocyte lineage transcription factor Olig2 using NG2creER™:Olig2fl/fl:ZEG triple transgenic mice did not increase the number of EGFP+ reactive astrocytes. These findings suggest that NG2 cells are not a major source of reactive astrocytes in the neocortex.

Original languageEnglish (US)
Pages (from-to)800-809
Number of pages10
Issue number5
StatePublished - May 2011


  • NG2
  • Oligodendrocyte
  • Reactive astrocyte

ASJC Scopus subject areas

  • Neurology
  • Cellular and Molecular Neuroscience


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