Varela Carolina, Igartua Itziar, De la Rosa Enrique J, De la Villa Pedro
Department of Physiology, University of Alcala, Alcala de Henares, E-28871, Madrid, Spain.
Vision Res. 2003 Apr;43(8):879-85. doi: 10.1016/s0042-6989(02)00493-5.
The rd mouse has been widely used as an animal model of retinitis pigmentosa. In this model, a mutation of rod-specific phosphodiesterase leads to a loss of rods during the early period of postnatal life. Morphological modifications at the level of the outer plexiform layer have been shown (Proc. Nat. Acad. Sci. USA 97 (2000) 11020) in bipolar and horizontal cells. However, very little is known about the functional changes suffered by these cells postsynaptic to the degenerated rods. In the present work we have studied the neurotransmitter-induced currents in rod bipolar cells from the rd mouse retina. Currents induced by glutamate and GABA were studied by the patch clamp-whole cell technique, on rod bipolar cells enzymatically dissociated from the rd mouse retina. Data from rd animals were compared with non-dystrophic NMRI mice. GABA (30-100 micro M) and glutamate (100 micro M) were applied from a puff pipette in the near proximity of rod bipolar cell dendrites, clamped at physiological membrane potentials, and their evoked currents were studied. In rod bipolar cells from non-dystrophic mouse, puff application of glutamate induced an outward current. This current was increased twofold in absence of extracellular calcium (nominally 0 calcium). In rod bipolar cells from adult rd mouse, currents induced by glutamate were absent. Two types of GABA mediated currents were isolated in rod bipolar cells both in control and rd mouse retinas. The currents mediated by GABA(C) receptors were observed exclusively at the axon terminal, while the currents mediated by the GABA(A) receptors were observed upon GABA application to the bipolar cell dendrites. The currents mediated by GABA(A) receptors in rod bipolar cells from rd mouse were larger than those from control animals. We conclude that after the degeneration of rod photoreceptors in rd mouse, rod bipolar cells lost their glutamate (rod-neurotransmitter) input while they increase their response to GABA (horizontal cell-neurotransmitter). In our opinion, this work describes for the first time the changes in neurotransmitter sensitivity that affect rod bipolar cells after photoreceptor degeneration of the mouse retina.
rd 小鼠已被广泛用作视网膜色素变性的动物模型。在该模型中,视杆细胞特异性磷酸二酯酶的突变导致出生后早期视杆细胞丧失。双极细胞和水平细胞中外网状层水平的形态学改变已有报道(《美国国家科学院院刊》97 (2000) 11020)。然而,对于这些细胞在退化视杆细胞突触后所经历的功能变化却知之甚少。在本研究中,我们研究了来自 rd 小鼠视网膜的视杆双极细胞中神经递质诱导的电流。通过膜片钳全细胞技术,对从 rd 小鼠视网膜酶解分离的视杆双极细胞,研究了谷氨酸和 GABA 诱导的电流。将 rd 动物的数据与非营养不良的NMRI小鼠的数据进行比较。将 GABA(30 - 100 μM)和谷氨酸(100 μM)从靠近视杆双极细胞树突的喷管施加,钳制在生理膜电位,研究它们诱发的电流。在非营养不良小鼠的视杆双极细胞中,局部施加谷氨酸诱导出外向电流。在无细胞外钙(名义上为 0 钙)时,该电流增加两倍。在成年 rd 小鼠的视杆双极细胞中,谷氨酸诱导的电流缺失。在对照和 rd 小鼠视网膜的视杆双极细胞中均分离出两种类型的 GABA 介导电流。由 GABA(C) 受体介导的电流仅在轴突末端观察到,而由 GABA(A) 受体介导的电流在将 GABA 施加到双极细胞树突时观察到。来自 rd 小鼠视杆双极细胞中由 GABA(A) 受体介导的电流大于对照动物的电流。我们得出结论,在 rd 小鼠视杆光感受器退化后,视杆双极细胞失去了它们的谷氨酸(视杆神经递质)输入,同时它们对 GABA(水平细胞神经递质)的反应增强。我们认为,这项工作首次描述了小鼠视网膜光感受器退化后影响视杆双极细胞的神经递质敏感性变化。