Ferguson Shawn M, Savchenko Valentina, Apparsundaram Subbu, Zwick Melissa, Wright Jane, Heilman Craig J, Yi Hong, Levey Allan I, Blakely Randy D
Neuroscience Graduate Program, Center for Molecular Neuroscience, Vanderbilt University, Nashville, Tennessee 37232, USA.
J Neurosci. 2003 Oct 29;23(30):9697-709. doi: 10.1523/JNEUROSCI.23-30-09697.2003.
Presynaptic synthesis of acetylcholine (ACh) requires a steady supply of choline, acquired by a plasma membrane, hemicholinium-3-sensitive (HC-3) choline transporter (CHT). A significant fraction of synaptic choline is recovered from ACh hydrolyzed by acetylcholinesterase (AChE) after vesicular release. Although antecedent neuronal activity is known to dictate presynaptic CHT activity, the mechanisms supporting this regulation are unknown. We observe an exclusive localization of CHT to cholinergic neurons and demonstrate that the majority of CHTs reside on small vesicles within cholinergic presynaptic terminals in the rat and mouse brain. Furthermore, immunoisolation of presynaptic vesicles with multiple antibodies reveals that CHT-positive vesicles carry the vesicular acetylcholine transporter (VAChT) and synaptic vesicle markers such as synaptophysin and Rab3A and also contain acetylcholine. Depolarization of synaptosomes evokes a Ca2+-dependent botulinum neurotoxin C-sensitive increase in the Vmax for HC-3-sensitive choline uptake that is accompanied by an increase in the density of CHTs in the synaptic plasma membrane. Our study leads to the novel hypothesis that CHTs reside on a subpopulation of synaptic vesicles in cholinergic terminals that can transit to the plasma membrane in response to neuronal activity to couple levels of choline re-uptake to the rate of ACh release.
乙酰胆碱(ACh)的突触前合成需要通过质膜上对高半胱氨酸-3敏感(HC-3)的胆碱转运体(CHT)稳定供应胆碱。突触胆碱的很大一部分是在囊泡释放后从被乙酰胆碱酯酶(AChE)水解的ACh中回收的。虽然已知先前的神经元活动决定突触前CHT的活性,但支持这种调节的机制尚不清楚。我们观察到CHT在胆碱能神经元中特异性定位,并证明大多数CHT存在于大鼠和小鼠脑中胆碱能突触前终末内的小囊泡上。此外,用多种抗体对突触前囊泡进行免疫分离显示,CHT阳性囊泡携带囊泡乙酰胆碱转运体(VAChT)和突触囊泡标记物,如突触素和Rab3A,并且还含有乙酰胆碱。突触体去极化引起对HC-3敏感的胆碱摄取的Vmax出现Ca2+依赖性肉毒杆菌神经毒素C敏感增加,同时伴随着突触质膜中CHT密度的增加。我们的研究提出了一个新的假设,即CHT存在于胆碱能终末的一部分突触囊泡上,这些囊泡可响应神经元活动而转运到质膜,从而使胆碱再摄取水平与ACh释放速率相耦合。