Involvement of BDNF Receptor TrkB in Spatial Memory Formation

  1. Makoto Mizuno2,
  2. Kiyofumi Yamada1,2,3,
  3. Jue He,
  4. Akira Nakajima, and
  5. Toshitaka Nabeshima3
  1. Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya 466-8560, Japan

Abstract

The N-methyl-D-aspartate (NMDA) receptors are involved in long-term potentiation (LTP), and are phosphorylated by several tyrosine kinases including a Src-family tyrosine kinase Fyn. Brain-derived neurotrophic factor (BDNF) is a neurotrophin, which also enhances hippocampal synaptic transmission and efficacy by increasing NMDA receptor activity. Here, we show that Fyn is a key molecule linking the BDNF receptor TrkB with NMDA receptors, which play an important role in spatial memory formation in a radial arm maze. Spatial learning induced phosphorylation of TrkB, Fyn, and NR2B, but not NR2A, in the hippocampus. Fyn was coimmunoprecipitated with TrkB and NR2B, and this association was increased in well-trained rats compared with control animals. Continuous intracerebroventricular infusion of PP2, a tyrosine kinase inhibitor, in rats delayed memory acquisition in the radial arm maze, but PP2-treated animals reached the same level of learning as the controls. The phosphorylation of Fyn and NR2B, but not TrkB, was diminished by PP2 treatment. Our findings suggest the importance of interaction between BDNF/TrkB signaling and NMDA receptors for spatial memory in the hippocampus.

Footnotes

  • 1 Present address: Laboratory of Experimental Therapeutics, Department of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Kanazawa University, Kanazawa 920-0934, Japan.

  • 2 These authors contributed equally to this work.

  • 3 Corresponding authors.

  • E-MAIL tnabeshi{at}med.nagoya-u.ac.jp; FAX 81-52-744-2682.

  • E-MAIL kyamada{at}p.kanazawa-u.ac.jp; FAX 81-76-234-4493.

  • Article and publication are at http://www.learnmem.org/cgi/doi/10.1101/lm.56003.

    • Received October 1, 2002.
    • Accepted February 3, 2003.
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