Correlation Engine 2.0
Clear Search sequence regions


  • adult (4)
  • brain (1)
  • hindbrain (4)
  • humans (1)
  • Leu9 (2)
  • mesencephalon (1)
  • mice (4)
  • midbrain (2)
  • nAChR (2)
  • neural stem cell (2)
  • neurogenesis (5)
  • receptors (2)
  • rhombencephalon (1)
  • α synuclein (3)
  • Sizes of these terms reflect their relevance to your search.

    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. 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). 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. 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. 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.

    Citation

    Mareike Fauser, Francisco Pan-Montojo, Christian Richter, Philipp J Kahle, Sigrid C Schwarz, Johannes Schwarz, Alexander Storch, Andreas Hermann. Chronic-Progressive Dopaminergic Deficiency Does Not Induce Midbrain Neurogenesis. Cells. 2021 Mar 31;10(4)

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 33807497

    View Full Text