Hu Jiang-Yuan, Glickman Leonard, Wu Fang, Schacher Samuel
Center for Neurobiology and Behavior, Columbia University College of Physicians and Surgeons, New York State Psychiatric Institute, 1051 Riverside Drive, New York, NY 10032, USA.
Neuron. 2004 Aug 5;43(3):373-85. doi: 10.1016/j.neuron.2004.07.011.
In Aplysia, long-term facilitation (LTF) of sensory neuron synapses requires activation of both protein kinase A (PKA) and mitogen-activated protein kinase (MAPK). We find that 5-HT through activation of PKA regulates secretion of the sensory neuron-specific neuropeptide sensorin, which binds autoreceptors to activate MAPK. Anti-sensorin antibody blocked LTF and MAPK activation produced by 5-HT and LTF produced by medium containing sensorin that was secreted from sensory neurons after 5-HT treatment. A single application of 5-HT followed by a 2 hr incubation with sensorin produced protein synthesis-dependent LTF, growth of new presynaptic varicosities, and activation of MAPK and its translocation into sensory neuron nuclei. Inhibiting PKA during 5-HT applications and inhibiting receptor tyrosine kinase or MAPK during sensorin application blocked both LTF and MAPK activation and translocation. Thus, long-term synaptic plasticity is produced when stimuli activate kinases in a specific sequence by regulating the secretion and autocrine action of a neuropeptide.
在海兔中,感觉神经元突触的长期易化(LTF)需要蛋白激酶A(PKA)和丝裂原活化蛋白激酶(MAPK)的共同激活。我们发现,5-羟色胺(5-HT)通过激活PKA来调节感觉神经元特异性神经肽传感蛋白的分泌,该神经肽与自身受体结合以激活MAPK。抗传感蛋白抗体阻断了5-HT产生的LTF和MAPK激活,以及由5-HT处理后感觉神经元分泌的含传感蛋白的培养基所产生的LTF。单次应用5-HT,随后与传感蛋白孵育2小时,可产生蛋白质合成依赖性LTF、新的突触前膨体生长以及MAPK的激活及其向感觉神经元细胞核的转位。在应用5-HT期间抑制PKA,以及在应用传感蛋白期间抑制受体酪氨酸激酶或MAPK,均可阻断LTF以及MAPK的激活和转位。因此,当刺激通过调节神经肽的分泌和自分泌作用以特定顺序激活激酶时,就会产生长期突触可塑性。