Conforti L, Tohse N, Sperelakis N
Department of Physiology and Biophysics, College of Medicine, University of Cincinnati, Ohio 45267.
J Dev Physiol. 1991 Apr;15(4):237-46.
Co-cultures of rat ventricular myocytes and sympathetic neurons were established. Superior cervical ganglia and ventricles from newborn rats were enzymatically dissociated and plated in a culture dish. Experiments were done between the 3rd (when evidence of neuron-myocyte proximity arises) and the 5th day in culture (before the myocytes become confluent). Simultaneous intracellular recording from a cardiomyocyte and an attached neuron was done using conventional microelectrode techniques (resistance of 60-100 Mohm). The myocytes in co-culture were either quiescent or spontaneously contracting. The contracting cells were either latent pacemaker or ventricular-like myocytes. The action potential (AP) characteristics of cardiomyocytes in co-cultures were comparable to those recorded in cardiomyocytes in pure cultures. Sympathetic innervation of the cardiomyocytes in co-cultures was evidenced by stimulating the neuron and observing an increase in rate of beating in latent pacemaker myocytes (average increase of 19.4 +/- 4.6%). In quiescent cardiomyocytes, neural stimulation evoked a slow depolarization that can reach threshold and initiate APs in the cell. This response is similar to slow excitatory postsynaptic potentials (EPSPs) observed in other synapses. Slow ESPSs could also be recorded in spontaneous beating cells, made quiescent by nifedipine (1x10(-6)-1x10(-7) M). These results indicate that functional synaptic contacts are developed in co-culture of sympathetic neurons and cardiac myocytes, and slow EPSPs can be evoked in cardiomyocytes as well as in other excitable cells. The sympathetic innervation occurring in culture did not significantly modify the spontaneous AP characteristics of the cardiomyocytes.
建立了大鼠心室肌细胞与交感神经元的共培养体系。将新生大鼠的颈上神经节和心室进行酶解,然后接种于培养皿中。实验在培养的第3天(此时出现神经元与肌细胞接近的迹象)至第5天(在肌细胞汇合之前)进行。使用传统微电极技术(电阻为60 - 100兆欧)对心肌细胞和相连的神经元进行同步细胞内记录。共培养中的肌细胞要么静止,要么自发收缩。收缩细胞要么是潜在起搏细胞,要么是心室样肌细胞。共培养体系中心肌细胞的动作电位(AP)特征与纯培养心肌细胞中记录到的特征相当。通过刺激神经元并观察潜在起搏肌细胞的搏动速率增加(平均增加19.4±4.6%),证明了共培养体系中心肌细胞的交感神经支配。在静止的心肌细胞中,神经刺激引发缓慢去极化,该去极化可达到阈值并引发细胞中的动作电位。这种反应类似于在其他突触中观察到的缓慢兴奋性突触后电位(EPSP)。在硝苯地平(1×10⁻⁶ - 1×10⁻⁷ M)使自发搏动细胞静止后,也可记录到缓慢的EPSP。这些结果表明,在交感神经元与心肌细胞的共培养中形成了功能性突触联系,并且在心肌细胞以及其他可兴奋细胞中均可诱发缓慢的EPSP。共培养中发生的交感神经支配并未显著改变心肌细胞的自发动作电位特征。