MANF Promotes Differentiation and Migration of Neural Progenitor Cells With Potential Neural Regenerative Effects in Stroke

Mol Ther. 2018 Jan 3;26(1):238-255. doi: 10.1016/j.ymthe.2017.09.019. Epub 2017 Sep 21.

Abstract

Cerebral ischemia activates endogenous reparative processes, such as increased proliferation of neural stem cells (NSCs) in the subventricular zone (SVZ) and migration of neural progenitor cells (NPCs) toward the ischemic area. However, this reparative process is limited because most of the NPCs die shortly after injury or are unable to arrive at the infarct boundary. In this study, we demonstrate for the first time that endogenous mesencephalic astrocyte-derived neurotrophic factor (MANF) protects NSCs against oxygen-glucose-deprivation-induced injury and has a crucial role in regulating NPC migration. In NSC cultures, MANF protein administration did not affect growth of cells but triggered neuronal and glial differentiation, followed by activation of STAT3. In SVZ explants, MANF overexpression facilitated cell migration and activated the STAT3 and ERK1/2 pathway. Using a rat model of cortical stroke, intracerebroventricular injections of MANF did not affect cell proliferation in the SVZ, but promoted migration of doublecortin (DCX)+ cells toward the corpus callosum and infarct boundary on day 14 post-stroke. Long-term infusion of MANF into the peri-infarct zone increased the recruitment of DCX+ cells in the infarct area. In conclusion, our data demonstrate a neuroregenerative activity of MANF that facilitates differentiation and migration of NPCs, thereby increasing recruitment of neuroblasts in stroke cortex.

Keywords: Armet; Armetl1; cdnf; cerebral dopamine-derived neurotrophic factor; manf; mesencephalic astrocyte-derived neurotrophic factor; neuroblast; neurogenesis; neuronal migration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / cytology
  • Astrocytes / metabolism
  • Brain / metabolism
  • Brain / pathology
  • Cell Death
  • Cell Differentiation / genetics*
  • Cell Self Renewal / genetics
  • Cells, Cultured
  • Disease Models, Animal
  • Fluorescent Antibody Technique
  • Gene Expression
  • Immunohistochemistry
  • Mice
  • Mice, Knockout
  • Nerve Growth Factors / genetics*
  • Nerve Regeneration / genetics*
  • Neural Stem Cells / cytology*
  • Neural Stem Cells / metabolism*
  • Neuroglia / cytology
  • Neuroglia / metabolism
  • Neurons / cytology
  • Neurons / metabolism
  • STAT3 Transcription Factor / metabolism
  • Stress, Physiological
  • Stroke / genetics*
  • Stroke / metabolism
  • Stroke / pathology

Substances

  • MANF protein, mouse
  • Nerve Growth Factors
  • STAT3 Transcription Factor