Brain-derived neurotrophic factor-mediated retrograde signaling required for the induction of long-term potentiation at inhibitory synapses of visual cortical pyramidal neurons

• DOI: 10.1016/j.neures.2008.02.006
• Publication Date: 2008-04-21T20:33:06Z
• Authors: Tsuyoshi Inagaki; Tahamina Begum; Faruque Reza; Shoko Horibe; Mie Inaba; Yumiko Yoshimura; Yukio Komatsu
• Keywords: 0303 health sciences; Patch-Clamp Techniques; Brain-Derived Neurotrophic Factor; Pyramidal Cells; Long-Term Potentiation; Carbazoles; Electric Stimulation; Indole Alkaloids; Rats; 03 medical and health sciences; Organ Culture Techniques; Synapses; Animals; Receptor, trkB; Rats, Long-Evans; Enzyme Inhibitors; Signal Transduction; Visual Cortex

High-frequency stimulation (HFS) induces long-term potentiation (LTP) at inhibitory synapses of layer 5 pyramidal neurons in developing rat visual cortex. This LTP requires postsynaptic Ca2+ rise for induction, while the maintenance mechanism is present at the presynaptic site, suggesting presynaptic LTP expression and the necessity of retrograde signaling. We investigated whether the supposed signal is mediated by brain-derived neurotrophic factor (BDNF), which is expressed in pyramidal neurons but not inhibitory interneurons. LTP did not occur when HFS was applied in the presence of the Trk receptor tyrosine kinase inhibitor K252a in the perfusion medium. HFS produced LTP when bath application of K252a was started after HFS or when K252a was loaded into postsynaptic cells. LTP did not occur in the presence of TrkB-IgG scavenging BDNF or function-blocking anti-BDNF antibody in the medium. In cells loaded with the Ca2+ chelator BAPTA, the addition of BDNF to the medium enabled HFS to induce LTP without affecting baseline synaptic transmission. These results suggest that BDNF released from postsynaptic cells activates presynaptic TrkB, leading to LTP. Because BDNF, expressed activity dependently, regulates the maturation of cortical inhibition, inhibitory LTP may contribute to this developmental process, and hence experience-dependent functional maturation of visual cortex.