Pakhotin Pavel, Verkhratsky Alexei
The University of Manchester, School of Biological Sciences, Oxford Road, Manchester M13 9PT, UK.
Mol Cell Neurosci. 2005 Jan;28(1):79-84. doi: 10.1016/j.mcn.2004.08.014.
In the present study, we directly demonstrated electrical coupling between Bergmann glial cells (BG) and Purkinje neurones (PN) in acutely isolated cerebellar slices, prepared from 15 to 30 days old Sprague-Dawley rats. Electrical coupling between these two cells was identified by dual whole-cell voltage clamp, which allowed direct recording of junctional current. Whole-cell recordings from PN-PN, PN-BG and BG-BG pairs were made using Nomarski optics and infrared visualisation, which allowed precise morphological identification of cells. Junctional currents were recorded by applying hyper/and depolarising voltage sequences ranging from -120 to +40 mV (voltage step 10 mV) to one of the cells in the pair, while ion currents were measured from both cells. As has been shown before, junctional currents were frequently observed in BG-BG pairs: we found electrical coupling in 27 out of 34 pairs analysed. When the similar protocol was applied to the PN-BG pairs, junctional currents were found in 61 out of 87 pairs analysed. The electrical coupling was bi-directional as similar junctional currents were observed in PN when voltage step protocol was applied to BG. No electrical coupling was observed in PN-PN pairs (n = 21). To correlate the appearance of these currents with gap junctions we treated slices with octanol (200 microM) or halothane (500 microM)-known inhibitors of gap junction conductance. Both agents applied for 5 min resulted in a complete inhibition of junctional currents in PN-BG pair. The washout (15 min) led to a complete recovery of junctional currents after treatment with octanol; the action of halothane was irreversible. Finally, we found that filling the BG by Alexa Fluor 488 results in staining of adjacent PN (in 11 out of 23 pairs tested). We conclude therefore that cerebellar neurones and glial cells are directly connected via gap junctions.
在本研究中,我们直接证明了在从15至30日龄的Sprague-Dawley大鼠制备的急性分离的小脑切片中,伯格曼胶质细胞(BG)与浦肯野神经元(PN)之间存在电耦合。通过双全细胞膜片钳鉴定这两种细胞之间的电耦合,该方法允许直接记录连接电流。使用诺马斯基光学显微镜和红外可视化技术对PN-PN、PN-BG和BG-BG细胞对进行全细胞记录,从而能够对细胞进行精确的形态学鉴定。通过向细胞对中的一个细胞施加范围为-120至+40 mV(电压步长10 mV)的超极化/去极化电压序列来记录连接电流,同时测量两个细胞的离子电流。如之前所示,在BG-BG细胞对中经常观察到连接电流:在分析的34对细胞中有27对发现了电耦合。当将类似的方案应用于PN-BG细胞对时,在分析的87对细胞中有61对发现了连接电流。电耦合是双向的,因为当将电压步长方案应用于BG时,在PN中观察到了类似的连接电流。在PN-PN细胞对中未观察到电耦合(n = 21)。为了将这些电流的出现与缝隙连接相关联,我们用辛醇(200 microM)或氟烷(500 microM)(已知的缝隙连接电导抑制剂)处理切片。两种试剂均施加5分钟导致PN-BG细胞对中的连接电流完全被抑制。洗脱(15分钟)导致用辛醇处理后连接电流完全恢复;氟烷的作用是不可逆的。最后,我们发现用Alexa Fluor 488填充BG会导致相邻PN染色(在测试的23对细胞中有11对)。因此,我们得出结论,小脑神经元和胶质细胞通过缝隙连接直接相连。