Whim M D, Niemann H, Kaczmarek L K
Department of Pharmacology, Yale University School of Medicine, New Haven, Connecticut 06520-8066, USA.
J Neurosci. 1997 Apr 1;17(7):2338-47. doi: 10.1523/JNEUROSCI.17-07-02338.1997.
It is not yet understood how the molecular mechanisms controlling the release of neuropeptides differ from those controlling the release of classical transmitters, mainly because there are few peptidergic synapses in which the environment at the presynaptic release sites can be manipulated. Using Aplysia californica neuron B2, which synthesizes both peptide and classical transmitters, we have established two synaptic types. When B2 is cocultured with a sensory neuron, a peptidergic synapse is formed. In contrast, when B2 is cocultured with neuron B6, a classical synapse is formed. In contrast to a common assumption, single action potentials can release both types of transmitters. The secretion of peptide and classical transmitters by B2 is inhibited by the presynaptic injection of tetanus toxin, but not by an inactive mutant. Thus a synaptobrevin-like molecule is involved in the secretion of these two types of transmitters.
目前尚不清楚控制神经肽释放的分子机制与控制经典递质释放的分子机制有何不同,主要是因为几乎没有肽能突触,其中突触前释放位点的环境可以被操纵。利用既能合成肽又能合成经典递质的加州海兔神经元B2,我们建立了两种突触类型。当B2与感觉神经元共培养时,形成肽能突触。相反,当B2与神经元B6共培养时,形成经典突触。与通常的假设相反,单个动作电位可以释放两种类型的递质。B2分泌肽和经典递质受到突触前注射破伤风毒素的抑制,但不受无活性突变体的抑制。因此,一种类似于突触融合蛋白的分子参与了这两种类型递质的分泌。