A single-cell analysis reveals multiple roles of oligodendroglial lineage cells during post-ischemic regeneration

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

Abstract

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.

Detaljer

Författare
  • Martin Valny
  • Pavel Honsa
  • Eliska Waloschkova
  • Hana Matuskova
  • Jan Kriska
  • Denisa Kirdajova
  • Peter Androvic
  • Lukas Valihrach
  • Mikael Kubista
  • Miroslava Anderova
Externa organisationer
  • Charles University in Prague
  • Institute of Experimental Medicine, Czech Academy of Science
Forskningsområden

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Neurovetenskaper
Originalspråkengelska
Sidor (från-till)1068-1081
Antal sidor14
TidskriftGLIA
Volym66
Utgivningsnummer5
StatusPublished - 2018 maj
PublikationskategoriForskning
Peer review utfördJa
Externt publiceradJa