Potter D D, Landis S C, Matsumoto S G, Furshpan E J
J Neurosci. 1986 Apr;6(4):1080-98. doi: 10.1523/JNEUROSCI.06-04-01080.1986.
This is the second in a series of papers that describes the use of a sensitive microculture procedure to investigate the transmitter status of sympathetic neurons. Cultured immature principal neurons, dissociated from the superior cervical ganglia of newborn rats, are known to be plastic with respect to transmitter status; under certain culture conditions, populations of neurons that display (at least) adrenergic properties at the outset can be induced to display a variety of cholinergic properties, including the formation of functional neuron-neuron cholinergic synapses, as adrenergic properties decline. With the microculture procedure described in the preceding paper (Furshpan et al., 1986a), we have examined the transmitter status of individual neonate-derived neurons during this transition. Many such neurons secreted both norepinephrine and ACh (adrenergic/cholinergic dual function); examination of such neurons with the EM revealed a mixed population of synaptic vesicles. Direct evidence for a transition via this dual status was obtained by serial physiological assays of 14 neurons. The neonate-derived neurons were markedly heterogeneous in the rate of change of transmitter status. Principal neurons derived from adult superior cervical ganglia also displayed dual status, but the incidence was lower than in neonate-derived neurons cultured for similar periods. In preliminary serial assays of adult-derived neurons, many of the neurons did not acquire detectable cholinergic function, but in two cases evidence consistent with plasticity was obtained. While it is known that several types of neurons will form functional junctions in the presence of agents that block electrical activity, sympathetic principal neurons have apparently not been tested. In microculture, neuron-neuron synapses and junctions with cardiac myocytes were formed by sympathetic neurons grown chronically in the presence of blocking concentrations of TTX and hexamethonium.
这是一系列论文中的第二篇,该系列描述了使用一种灵敏的微培养程序来研究交感神经元的递质状态。从新生大鼠颈上神经节分离培养的未成熟主神经元,已知其在递质状态方面具有可塑性;在某些培养条件下,一开始表现出(至少)肾上腺素能特性的神经元群体,随着肾上腺素能特性的下降,可被诱导表现出多种胆碱能特性,包括形成功能性神经元 - 神经元胆碱能突触。利用前一篇论文(Furshpan等人,1986a)中描述的微培养程序,我们在此转变过程中检查了单个新生神经元的递质状态。许多这样的神经元同时分泌去甲肾上腺素和乙酰胆碱(肾上腺素能/胆碱能双重功能);用电镜检查此类神经元发现了混合的突触小泡群体。通过对14个神经元进行系列生理测定,获得了通过这种双重状态转变的直接证据。新生神经元在递质状态变化速率上明显异质性。源自成年大鼠颈上神经节的主神经元也表现出双重状态,但发生率低于培养相似时间的新生神经元。在对成年神经元的初步系列测定中,许多神经元未获得可检测到的胆碱能功能,但在两个案例中获得了与可塑性一致的证据。虽然已知几种类型的神经元在存在阻断电活动的试剂时会形成功能性连接,但交感主神经元显然尚未经过测试。在微培养中,交感神经元在存在阻断浓度的河豚毒素和六甲铵的情况下长期生长,形成了神经元 - 神经元突触以及与心肌细胞的连接。