Chan E, Yung W H, Baumann K I
Department of Physiology, Faculty of Medicine, Chinese University of Hong Kong, Shatin, N.T., Hong Kong.
Exp Brain Res. 1996 Mar;108(3):357-66. doi: 10.1007/BF00227259.
An isolated, functioning sinus hair preparation was developed to investigate cytoplasmic Ca2+ concentrations in intact Merkel cells using microfluorimetric techniques. Intracellular Ca2+ levels were monitored by means of photon counters in small groups of Merkel cells loaded with the calcium fluorescent indicators fura-2 or fluo-3. Mechanical stimulation of Merkel cells with fine glass rods resulted in small transient increases in intracellular Ca2+ levels (by about 20%) in the group of Merkel cells around the stimulating probe. A rise in Ca2+ is presumed to be essential for the postulated synaptic transmission to the afferent nerve terminal. Depolarization with a high concentration of potassium chloride (100 mM) caused increases in intracellular Ca2+ concentrations in Merkel cells (by about 70%) only in the presence of extracellular Ca2+, indicating an influx of Ca2+ through voltage-gated channels. The Ca2+ response was abolished neither by (+)-BayK8644 nor omega-conotoxin, suggesting that the Ca2+ channels are different from the classical L- or N-type channels. Extracellular application of ATP (10 microM to 5 mM) caused dose-dependent increases in intracellular Ca2+ levels in Merkel cells of up to sevenfold from the basal level of about 100 nM. Similar responses to ATP were also measured during superfusion with Ca(2+)-free medium, suggesting intracellular stores as the main Ca2+ source. Pre-incubation of Merkel cells with the purinoceptor antagonist suramin (100 microM) for 30 min reduced the Ca2+ responses to ATP by about 50% compared with control conditions. In conclusion, the results have demonstrated that a rise in intracellular Ca2+ in Merkel cells can be evoked by mechanical stimulation, membrane depolarization and chemical stimulation by ATP. These observations strongly suggest a possible contribution of Ca2+ to the normal responsiveness of Merkel cell mechanoreceptors, in turn supporting the hypothesis that Merkel cells are involved in the mechano-electric transduction process in sinus hair type I mechanoreceptors.
为了使用显微荧光技术研究完整默克尔细胞中的细胞质钙离子浓度,开发了一种分离的、具有功能的窦毛制备方法。通过光子计数器监测小群加载了钙荧光指示剂fura-2或fluo-3的默克尔细胞中的细胞内钙离子水平。用细玻璃棒对默克尔细胞进行机械刺激,导致刺激探针周围的默克尔细胞群中细胞内钙离子水平出现小幅度的瞬时升高(约20%)。钙离子的升高被认为是假定的向传入神经末梢的突触传递所必需的。仅在细胞外钙离子存在的情况下,用高浓度氯化钾(100 mM)进行去极化会导致默克尔细胞中细胞内钙离子浓度升高(约70%),这表明钙离子通过电压门控通道内流。(+)-BayK8644和ω-芋螺毒素均未消除钙离子反应,这表明钙离子通道不同于经典的L型或N型通道。细胞外施加ATP(10 μM至5 mM)导致默克尔细胞中细胞内钙离子水平呈剂量依赖性升高,最高可达基础水平约100 nM的七倍。在无钙培养基灌流期间也测量到了对ATP的类似反应,这表明细胞内储存是主要的钙离子来源。与对照条件相比,将默克尔细胞与嘌呤受体拮抗剂苏拉明(100 μM)预孵育30分钟可使对ATP的钙离子反应降低约50%。总之,结果表明机械刺激、膜去极化和ATP的化学刺激均可引起默克尔细胞中细胞内钙离子升高。这些观察结果强烈表明钙离子可能对默克尔细胞机械感受器的正常反应性有贡献,进而支持了默克尔细胞参与窦毛I型机械感受器机械电转换过程的假说。