Expression of Transcription Factor ZBTB20 in the Adult Primate Neurogenic Niche under Physiological Conditions or after Ischemia

Genes (Basel). 2022 Aug 29;13(9):1559. doi: 10.3390/genes13091559.

Abstract

The Zbtb20 gene encodes for a transcription factor that plays an important role in mammalian cortical development. Recently, its expression was reported in the adult mouse subventricular zone (SVZ), a major neurogenic niche containing neural stem cells throughout life. Here, we analyzed its expression in the adult primate anterior SVZ (SVZa) and rostral migratory stream (RMS) using macaque monkeys (Macaca fuscata). We report that the majority of Ki67+ cells, 71.4% in the SVZa and 85.7% in the RMS, co-label for ZBTB20. Nearly all neuroblasts, identified by their Doublecortin expression, were positive for ZBTB20 in both regions. Nearly all GFAP+ neural stem cells/astrocytes were also positive for ZBTB20. Analysis of images derived from a public database of gene expression in control/ischemic monkey SVZa, showed evidence for ZBTB20 upregulation in postischemic monkey SVZa. Furthermore, the co-localization of ZBTB20 with Doublecortin and Ki67 was increased in the postischemic SVZa. Our results suggest that ZBTB20 expression is evolutionarily conserved in the mammalian neurogenic niche and is reactive to ischemia. This opens the possibility for further functional studies on the role of this transcription factor in neurogenesis in primates.

Keywords: ZBTB20; neural progenitor; non-human primate; subventricular zone.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Doublecortin Domain Proteins
  • Haplorhini
  • Ischemia
  • Ki-67 Antigen
  • Mammals
  • Mice
  • Neurogenesis* / genetics
  • Primates
  • Transcription Factors* / genetics

Substances

  • Doublecortin Domain Proteins
  • Ki-67 Antigen
  • Transcription Factors
  • Zbtb20 protein, mouse

Grants and funding

This work was supported by an intramural grant of the Medical University—Varna (21020/2021) and the National Program “European Research Networks” of the Bulgarian Ministry of Education and Science. M.I. is supported by the European Commission Horizon 2020 Framework Program (Project 856871—TRANSTEM).