Chronic-Progressive Dopaminergic Deficiency Does Not Induce Midbrain Neurogenesis

Cells. 2021 Mar 31;10(4):775. doi: 10.3390/cells10040775.

Abstract

Background: Consecutive adult neurogenesis is a well-known phenomenon in the ventricular-subventricular zone of the lateral wall of the lateral ventricles (V-SVZ) and has been controversially discussed in so-called "non-neurogenic" brain areas such as the periventricular regions (PVRs) of the aqueduct and the fourth ventricle. Dopamine is a known modulator of adult neural stem cell (aNSC) proliferation and dopaminergic neurogenesis in the olfactory bulb, though a possible interplay between local dopaminergic neurodegeneration and induction of aNSC proliferation in mid/hindbrain PVRs is currently enigmatic.

Objective/hypothesis: To analyze the influence of chronic-progressive dopaminergic neurodegeneration on both consecutive adult neurogenesis in the PVRs of the V-SVZ and mid/hindbrain aNSCs in two mechanistically different transgenic animal models of Parkinson´s disease (PD).

Methods: We used Thy1-m[A30P]h α synuclein mice and Leu9'Ser hypersensitive α4* nAChR mice to assess the influence of midbrain dopaminergic neuronal loss on neurogenic activity in the PVRs of the V-SVZ, the aqueduct and the fourth ventricle.

Results: In both animal models, overall proliferative activity in the V-SVZ was not altered, though the proportion of B2/activated B1 cells on all proliferating cells was reduced in the V-SVZ in Leu9'Ser hypersensitive α4* nAChR mice. Putative aNSCs in the mid/hindbrain PVRs are known to be quiescent in vivo in healthy controls, and dopaminergic deficiency did not induce proliferative activity in these regions in both disease models.

Conclusions: Our data do not support an activation of endogenous aNSCs in mid/hindbrain PVRs after local dopaminergic neurodegeneration. Spontaneous endogenous regeneration of dopaminergic cell loss through resident aNSCs is therefore unlikely.

Keywords: Parkinson´s disease; adult neurogenesis; dopaminergic neurodegeneration; non-neurogenic regions; periventricular regions; transgenic animal model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation
  • Dopamine / deficiency*
  • Humans
  • Lateral Ventricles / physiology
  • Mesencephalon / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Neurogenesis*
  • Receptors, Nicotinic / metabolism
  • Rhombencephalon / physiology
  • alpha-Synuclein / metabolism

Substances

  • Receptors, Nicotinic
  • alpha-Synuclein
  • Dopamine