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Phenotypic and functional heterogeneity of GFAP‐expressing cells in vitro: Differential expression of LeX/CD15 by GFAP‐expressing multipotent neural stem cells and non‐neurogenic astrocytes
Author(s) -
Imura Tetsuya,
Nakano Ichiro,
Kornblum Harley I.,
Sofroniew Michael V.
Publication year - 2006
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.20281
Subject(s) - biology , neural stem cell , phenotype , neuroscience , neurosphere , multipotent stem cell , cd15 , in vitro , microbiology and biotechnology , stem cell , adult stem cell , progenitor cell , gene , endothelial stem cell , genetics , cd34
Abstract Recent findings show that the predominant multipotent neural stem cells (NSCs) isolated from postnatal and adult mouse brain express glial fibrillary acid protein (GFAP), a protein commonly associated with astrocytes, and that primary astrocyte cultures can contain GFAP‐expressing cells that act as multipotent NSCs when transferred to neurogenic conditions. The relationship of GFAP‐expressing NSCs to GFAP‐expressing astrocytes is unclear, but has important implications. We compared the phenotype and neurogenic potential of GFAP‐expressing cells derived from different CNS regions and maintained in vitro under different conditions. Multiple labeling immunohistochemistry revealed that both primary astrocyte cultures and adherent neurogenic cultures derived from postnatal or adult periventricular tissue contained subpopulations of GFAP‐expressing cells that co‐expressed nestin and LeX/CD15, two molecules associated with NSCs. In contrast, GFAP‐expressing cells in similar cultures prepared from adult cerebral cortex did not express detectable levels of LeX/CD15, and exhibited no neurogenic potential. Fluorescence‐activated cell sorting (FACS) of both primary astrocyte cultures and adherent neurogenic cultures for LeX/CD15 showed that GFAP‐expressing cells competent to act as multipotent NSCs were concentrated in the LeX‐positive fraction. Using neurosphere assays and a transgenic ablation strategy, we confirmed that the predominant NSCs in primary astrocyte and adherent neurogenic cultures were GFAP‐expressing cells. These findings demonstrate that GFAP‐expressing cells derived from postnatal and adult forebrain are heterogeneous in both molecular phenotype and neurogenic potential in vitro, and that this heterogeneity exists before exposure to neurogenic conditions. The findings provide evidence that GFAP‐expressing NSCs are phenotypically and functionally distinct from non‐neurogenic astrocytes. © 2005 Wiley‐Liss, Inc.

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