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Trophic Factor-Induced Plasticity of Synaptic Connections Between Identified Lymnaea Neurons

机译:营养因子诱导可识别的lymnaea神经元之间的突触连接的可塑性。

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摘要

Neurotrophic factors participate in both developmental and adult synaptic plasticity; however, the underlying mechanisms remain unknown. Using soma–soma synapses between the identified Lymnaea neurons, we demonstrate that the brain conditioned medium (CM)-derived trophic factors are required for the formation of excitatory but not the inhibitory synapse. Specifically, identified presynaptic [right pedal dorsal 1 (RPeD1) and visceral dorsal 4 (VD4)] and postsynaptic [visceral dorsal 2/3 (VD2/3) and left pedal dorsal 1 (LPeD1)] neurons were soma–soma paired either in the absence or presence of CM. We show that in defined medium (DM—does not contain extrinsic trophic factors), appropriate excitatory synapses failed to develop between RPeD1 and VD2/3. Instead, inappropriate inhibitory synapses formed between VD2/3 and RPeD1. Similarly, mutual inhibitory synapses developed between VD4 and LPeD1 in DM. These inhibitory synapses were termed novel because they do not exist in the intact brain. To test whether DM-induced, inappropriate inhibitory synapses could be corrected by the addition of CM, cells were first paired in DM for an initial period of 12 hr. DM was then replaced with CM, and simultaneous intracellular recordings were made from paired cells after 6–12 hr of CM substitution. Not only did CM induce the formation of appropriate excitatory synapses between both cell pairs, but it also reduced the incidence of inappropriate inhibitory synapse formation. The CM-induced plasticity of synaptic connections involved new protein synthesis and transcription and was mediated via receptor tyrosine kinases. Taken together, our data provide the first direct insight into the cellular mechanism underlying trophic factor-induced specificity and plasticity of synaptic connections between soma–soma paired Lymnaea neurons.
机译:神经营养因子参与发育和成人突触可塑性。但是,其潜在机制仍然未知。使用确定的淋巴神经元之间的体细胞突触,我们证明了形成刺激性而不是抑制性突触所需的脑条件培养基(CM)衍生的营养因子。具体来说,已识别的突触前[右脚背背1(RPeD1)和内脏背4(VD4)]和突触后[内脏背背2/3(VD2 / 3)和左脚背背1(LPeD1)]神经元在两种情况下都为体-体配对CM是否存在。我们表明,在定义的培养基(DM-不包含外在营养因子)中,RPeD1和VD2 / 3之间不能发育出适当的兴奋性突触。而是在VD2 / 3和RPeD1之间形成了不适当的抑制突触。同样,DM中的VD4和LPeD1之间形成了相互抑制的突触。这些抑制性突触被称为新颖的,因为它们在完整的大脑中不存在。为了测试是否可以通过添加CM来纠正DM诱导的不适当的抑制性突触,首先将细胞在DM中配对12个小时。然后用CM替代DM,在CM替代6-12小时后,从配对细胞中同时进行细胞内记录。 CM不仅诱导了两个细胞对之间适当的兴奋性突触的形成,而且还减少了不适当的抑制性突触形成的发生率。 CM诱导的突触连接的可塑性涉及新的蛋白质合成和转录,并通过受体酪氨酸激酶介导。综上所述,我们的数据首次提供了直接的洞察力,揭示了营养因子诱导的体细胞配对淋巴神经元之间突触连接的特异性和可塑性的细胞机制。

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