Department of Physiology, School of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Rd., Wuhan, China.
Institutes of Brain Research, Huazhong University of Science and Technology, Wuhan, China.
J Physiol Biochem. 2018 May;74(2):207-221. doi: 10.1007/s13105-017-0606-9. Epub 2018 Jan 19.
The dissociated dorsal root ganglion (DRG) neurons with or without culture were widely used for investigation of their electrophysiological properties. The culture procedures, however, may alter the properties of these neurons and the effects are not clear. In the present study, we recorded the action potentials (AP) and the voltage-gated Na, K, and Ca currents with patch clamp technique and measured the mRNA of Nav1.6-1.9 and Cav2.1-2.2 with real-time PCR technique from acutely dissociated and 1-day (1-d) cultured DRG neurons. The effects of the nerve growth factor (NGF) on the expression of Nav1.6-1.9 and Cav2.1-2.2 were evaluated. The neurons were classified as small (DRG-S), medium (DRG-M), and large (DRG-L), according to their size frequency distribution pattern. We found 1-d culture increased the AP size but reduced the excitability, and reduced the voltage-gated Na and Ca currents and their corresponding mRNA expression in all types of neurons. The lack of NGF in the culture medium may contribute to the reduced Na and Ca current, as the application of NGF recovered some of the reduced transcripts (Nav1.9, Cav2.1, and Cav2.2). 1-d culture showed neuron-type specific effects on some of the AP properties: it increased the maximum AP depolarizing rate (MDR) and hyperpolarized the resting membrane potential (RP) in DRG-M and DRG-L neurons, but slowed the maximum AP repolarizing rate (MRR) in DRG-S neurons. In conclusion, the 1-d cultured neurons had different properties with those of the acutely dissociated neurons, and lack of NGF may contribute to some of these differences.
分离的背根神经节(DRG)神经元,无论是否进行培养,都广泛用于研究其电生理特性。然而,培养过程可能会改变这些神经元的特性,但其具体影响尚不清楚。在本研究中,我们采用膜片钳技术记录动作电位(AP)和电压门控钠、钾和钙电流,并采用实时 PCR 技术测量急性分离和培养 1 天(1-d)的 DRG 神经元中 Nav1.6-1.9 和 Cav2.1-2.2 的 mRNA。评估神经生长因子(NGF)对 Nav1.6-1.9 和 Cav2.1-2.2 表达的影响。根据神经元大小的频率分布模式,将神经元分为小(DRG-S)、中(DRG-M)和大(DRG-L)型。我们发现 1-d 培养增加了 AP 幅度,但降低了兴奋性,并减少了所有类型神经元的电压门控钠和钙电流及其相应的 mRNA 表达。培养物中缺乏 NGF 可能是导致钠和钙电流减少的原因,因为 NGF 的应用恢复了一些减少的转录本(Nav1.9、Cav2.1 和 Cav2.2)。1-d 培养对某些 AP 特性具有神经元类型特异性影响:它增加了 DRG-M 和 DRG-L 神经元的最大 AP 去极化率(MDR)并使静息膜电位(RP)超极化,但降低了 DRG-S 神经元的最大 AP 复极化率(MRR)。总之,1-d 培养的神经元具有与急性分离神经元不同的特性,而缺乏 NGF 可能是导致其中一些差异的原因之一。