A single-cell analysis reveals multiple roles of oligodendroglial lineage cells during post-ischemic regeneration
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29393544
DOI
10.1002/glia.23301
Knihovny.cz E-resources
- Keywords
- Alzheimer's, NG2 cells, astrocytes, cerebral ischemia, oligodendrocytes,
- MeSH
- Single-Cell Analysis MeSH
- Astrocytes pathology physiology MeSH
- Brain Ischemia pathology physiopathology MeSH
- Disease Models, Animal MeSH
- Brain pathology physiopathology MeSH
- Mice, Transgenic MeSH
- Oligodendrocyte Precursor Cells pathology physiology MeSH
- Cell Proliferation physiology MeSH
- Nerve Regeneration physiology MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
NG2 cells represent precursors of oligodendrocytes under physiological conditions; however, following cerebral ischemia they play an important role in glial scar formation. Here, we compared the expression profiles of oligodendroglial lineage cells, after focal cerebral ischemia (FCI) and in Alzheimer's-like pathology using transgenic mice, which enables genetic fate-mapping of Cspg4-positive NG2 cells and their progeny, based on the expression of red fluorescent protein tdTomato. tdTomato-positive cells possessed the expression profile of NG2 cells and oligodendrocytes; however, based on the expression of cell type-specific genes, we were able to distinguish between them. To shed light on the changes in the expression patterns caused by FCI, we employed self-organizing Kohonen maps, enabling the division of NG2 cells and oligodendrocytes into subpopulations based on similarities in the expression profiles of individual cells. We identified three subpopulations of NG2 cells emerging after FCI: proliferative; astrocyte-like and oligodendrocyte-like NG2 cells; such phenotypes were further confirmed by immunohistochemistry. Oligodendrocytes themselves formed four subpopulations, which reflected the process of oligodendrocytes maturation. Finally, we used 5-ethynyl-2' deoxyuridine (EdU) labeling to reveal that NG2 cells can differentiate directly into reactive astrocytes without preceding proliferation. In contrast, in Alzheimer's-like pathology we failed to identify these subpopulations. Collectively, here we identified several yet unknown differences between the expression profiles of NG2 cells and oligodendrocytes, and characterized specific genes contributing to oligodendrocyte maturation and phenotypical changes of NG2 cells after FCI. Moreover, our results suggest that, unlike in Alzheimer's-like pathology, NG2 cells acquire a multipotent phenotype following FCI.
References provided by Crossref.org
Out of the core: the impact of focal ischemia in regions beyond the penumbra
Astrocytic TRPV4 Channels and Their Role in Brain Ischemia
Transient astrocyte-like NG2 glia subpopulation emerges solely following permanent brain ischemia
On the Common Journey of Neural Cells through Ischemic Brain Injury and Alzheimer's Disease