Pothos E N, Larsen K E, Krantz D E, Liu Y, Haycock J W, Setlik W, Gershon M D, Edwards R H, Sulzer D
Departments of Neurology and Psychiatry, Columbia University, New York, New York 10032, USA.
J Neurosci. 2000 Oct 1;20(19):7297-306. doi: 10.1523/JNEUROSCI.20-19-07297.2000.
While the transporters that accumulate classical neurotransmitters in synaptic vesicles have been identified, little is known about how their expression regulates synaptic transmission. We have used adenoviral-mediated transfection to increase expression of the brain vesicular monoamine transporter VMAT2 and presynaptic amperometric recordings to characterize the effects on quantal release. In presynaptic axonal varicosities of ventral midbrain neurons in postnatal culture, VMAT2 overexpression in small synaptic vesicles increased both quantal size and frequency, consistent with the recruitment of synaptic vesicles that do not normally release dopamine. This was confirmed using noncatecholaminergic AtT-20 cells, in which VMAT2 expression induced the quantal release of dopamine. The ability to increase quantal size in vesicles that were already competent for dopamine release was shown in PC12 cells, in which VMAT2 expression increased the quantal size but not the number of release events. These results demonstrate that vesicle transporters limit the rate of transmitter accumulation and can alter synaptic strength through two distinct mechanisms.
虽然已鉴定出在突触小泡中积累经典神经递质的转运体,但对于它们的表达如何调节突触传递却知之甚少。我们利用腺病毒介导的转染来增加脑囊泡单胺转运体VMAT2的表达,并通过突触前安培测量记录来表征对量子释放的影响。在出生后培养的腹侧中脑神经元的突触前轴突膨体中,小突触小泡中VMAT2的过表达增加了量子大小和频率,这与通常不释放多巴胺的突触小泡的募集一致。使用非儿茶酚胺能AtT-20细胞证实了这一点,在该细胞中VMAT2的表达诱导了多巴胺的量子释放。在PC12细胞中显示了增加已经能够释放多巴胺的小泡中量子大小的能力,在PC12细胞中VMAT2的表达增加了量子大小,但没有增加释放事件的数量。这些结果表明,囊泡转运体限制了递质积累的速率,并可通过两种不同机制改变突触强度。