Neurochemical Research

, Volume 31, Issue 2, pp 215-225

First online:

The Polysialylated Neural Cell Adhesion Molecule Promotes Neurogenesis in vitro

  • Laszlo VutskitsAffiliated withDepartment of Anesthesiology, Pharmacology and Intensive Care, University Hospital of GenevaDepartment of Neuroscience, University of Geneva
  • , Eduardo GasconAffiliated withDepartment of Neuroscience, University of Geneva
  • , Eloisa ZgraggenAffiliated withDepartment of Neuroscience, University of Geneva
  • , Jozsef Zoltan KissAffiliated withDepartment of Neuroscience, University of GenevaDepartment of Neuroscience, University of Geneva Email author 

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A characteristic feature of neurogenic sites in the postnatal brain is the expression of the polysialylated forms of the neural cell adhesion molecule (PSA-NCAM). To investigate the role of PSA-NCAM in generation of neuronal populations, we developed an in vitro model where neurogenesis occurs in primary cortical cultures following serum withdrawal. We show that removal or inactivation of the PSA tail of NCAM in these cultures leads to a significant decrease in the number of newly generated neurons. Similarly, cultures prepared from NCAM knock-out mice exhibit a significantly reduced neurogenesis. Pulse-chase experiments using the proliferation marker BrdU reveal that the lack of PSA does not affect the mitotic rate of neural progenitors but rather, it reduces the early survival of newly generated neurons. These results suggest that, in addition to its role in the migration of neuronal progenitors, PSA-NCAM is required for the adequate survival of these cells.


Neuronal survival Postnatal neurogenesis PSA-NCAM Proliferation