Your browser doesn't support javascript.
loading
SAD-B kinase regulates pre-synaptic vesicular dynamics at hippocampal Schaffer collateral synapses and affects contextual fear memory.
Watabe, Ayako M; Nagase, Masashi; Hagiwara, Akari; Hida, Yamato; Tsuji, Megumi; Ochiai, Toshitaka; Kato, Fusao; Ohtsuka, Toshihisa.
Afiliación
  • Watabe AM; Department of Neuroscience, School of Medicine, Jikei University, Tokyo, Japan.
  • Nagase M; Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency, Kawaguchi, Saitama, Japan.
  • Hagiwara A; Department of Neuroscience, School of Medicine, Jikei University, Tokyo, Japan.
  • Hida Y; Department of Biochemistry, University of Yamanashi, Yamanashi, Japan.
  • Tsuji M; Department of Biochemistry, University of Yamanashi, Yamanashi, Japan.
  • Ochiai T; Department of Neuroscience, School of Medicine, Jikei University, Tokyo, Japan.
  • Kato F; Department of Neuroscience, School of Medicine, Jikei University, Tokyo, Japan.
  • Ohtsuka T; Department of Neuroscience, School of Medicine, Jikei University, Tokyo, Japan.
J Neurochem ; 136(1): 36-47, 2016 Jan.
Article en En | MEDLINE | ID: mdl-26444684
ABSTRACT
Synapses of amphids defective (SAD)-A/B kinases control various steps in neuronal development and differentiation, such as axon specifications and maturation in central and peripheral nervous systems. At mature pre-synaptic terminals, SAD-B is associated with synaptic vesicles and the active zone cytomatrix; however, how SAD-B regulates neurotransmission and synaptic plasticity in vivo remains unclear. Thus, we used SAD-B knockout (KO) mice to study the function of this pre-synaptic kinase in the brain. We found that the paired-pulse ratio was significantly enhanced at Shaffer collateral synapses in the hippocampal CA1 region in SAD-B KO mice compared with wild-type littermates. We also found that the frequency of the miniature excitatory post-synaptic current was decreased in SAD-B KO mice. Moreover, synaptic depression following prolonged low-frequency synaptic stimulation was significantly enhanced in SAD-B KO mice. These results suggest that SAD-B kinase regulates vesicular release probability at pre-synaptic terminals and is involved in vesicular trafficking and/or regulation of the readily releasable pool size. Finally, we found that hippocampus-dependent contextual fear learning was significantly impaired in SAD-B KO mice. These observations suggest that SAD-B kinase plays pivotal roles in controlling vesicular release properties and regulating hippocampal function in the mature brain. Synapses of amphids defective (SAD)-A/B kinases control various steps in neuronal development and differentiation, but their roles in mature brains were only partially known. Here, we demonstrated, at mature pre-synaptic terminals, that SAD-B regulates vesicular release probability and synaptic plasticity. Moreover, hippocampus-dependent contextual fear learning was significantly impaired in SAD-B KO mice, suggesting that SAD-B kinase plays pivotal roles in controlling vesicular release properties and regulating hippocampal function in the mature brain.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vesículas Sinápticas / Proteínas Serina-Treonina Quinasas / Terminales Presinápticos / Miedo / Hipocampo / Memoria Límite: Animals Idioma: En Revista: J Neurochem Año: 2016 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vesículas Sinápticas / Proteínas Serina-Treonina Quinasas / Terminales Presinápticos / Miedo / Hipocampo / Memoria Límite: Animals Idioma: En Revista: J Neurochem Año: 2016 Tipo del documento: Article País de afiliación: Japón