Cyclin-dependent kinase 5 activators p35 and p39 facilitate formation of functional synapses

Jenny U. Johansson, Lena Lilja, Xiao Liang Chen, Haruhiro Higashida, Björn Meister, Mami Noda, Zhen Guo Zhong, Shigeru Yokoyama, Per Olof Berggren, Christina Bark

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

Cyclin-dependent kinase 5 (Cdk5) has emerged as a key coordinator of cell signaling in neurite outgrowth. Cdk5 needs to associate with one of the regulatory proteins p35 or p39 to be an active enzyme. To investigate if Cdk5 plays a role in the establishment of functional synapses, we have characterized the expression of Cdk5, p35, and p39 in the neuroblastoma-glioma cell line NG108-15, and recorded postsynaptic activity in myotubes in response to presynaptic overexpression of Cdk5, p35, and p39. Endogenous Cdk5 and p35 protein levels increased with cellular differentiation and preferentially distributed to soluble pools, whereas the level of p39 protein remained low and primarily was present in membrane and cytoskeletal fractions. Transient transfection of a dominant-negative mutant of Cdk5 in NG108-15 cells and subsequent culturing on differentiating muscle cells resulted in a significant reduction in synaptic activity, as measured by postsynaptic miniature endplate potentials (mEPPs). Overexpression of either Cdk5/p35 or Cdk5/p39 resulted in a substantial increase in synaptic structures that displayed postsynaptic activities, as well as mEPP frequency. These findings demonstrate that Cdk5, p35, and p39 are endogenously expressed in NG108-15 cells, exhibit distinct subcellular localizations, and that both Cdk5/p35 and Cdk5/p39 are central in formation of functional synapses.

Original languageEnglish (US)
Pages (from-to)215-227
Number of pages13
JournalMolecular Brain Research
Volume138
Issue number2
DOIs
StatePublished - Aug 18 2005

Keywords

  • Acetylcholine
  • Cellular differentiation
  • Hybrid cell
  • Miniature endplate potential
  • Myotube
  • Synaptogenesis

ASJC Scopus subject areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience

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