Nasi E
Department of Physiology, Boston University School of Medicine, Massachusetts 02118.
J Gen Physiol. 1991 Jan;97(1):17-34. doi: 10.1085/jgp.97.1.17.
Photoreceptor cells were enzymatically dissociated from the eye of the file clam, Lima scabra. Micrographs of solitary cells reveal a villous rhabdomeric lobe, a smooth soma, and a heavily pigmented intermediate region. Membrane voltage recordings using patch electrodes show resting potentials around -60 mV. Input resistance ranges from 300 M omega to greater than 1 G omega, while membrane capacitance is of the order of 50-70 pF. In darkness, quantum bumps occur spontaneously and their frequency can be increased by dim continuous illumination in a fashion graded with light intensity. Stimulation with flashes of light produces a depolarizing photoresponse which is usually followed by a transient hyperpolarization if the stimulus is sufficiently intense. Changing the membrane potential with current-clamp causes the early phase to invert around +10 mV, while the hyperpolarizing dip disappears around -80 mV. With bright light, the biphasic response is followed by an additional depolarizing wave, often accompanied by a burst of action potentials. Both Na and Ca ions are required in the extracellular solution for normal photoexcitation: the response to flashes of moderate intensity is greatly degraded either when Na is replaced with Tris, or when Ca is substituted with Mg. By contrast, quantum bumps elicited by dim, sustained light are not affected by Ca removal, but they are markedly suppressed in a reversible way in 0 Na sea water. It was concluded that the generation of the receptor potential is primarily dependent on Na ions, whereas Ca is probably involved in a voltage-dependent process that shapes the photoresponse. Light adaptation by repetitive flashes leads to a decrease of the depolarizing phase and a concomitant enhancement of the hyperpolarizing dip, eventually resulting in a purely hyperpolarizing photoresponse. Dark adaptation restores the original biphasic shape of the photoresponse.
光感受器细胞是从锉蛤(Lima scabra)的眼中通过酶解分离得到的。单个细胞的显微照片显示出一个具绒毛的横纹肌叶、一个光滑的细胞体以及一个色素沉着严重的中间区域。使用膜片电极进行的膜电压记录显示静息电位约为 -60 mV。输入电阻范围从300 MΩ到大于1 GΩ,而膜电容约为50 - 70 pF。在黑暗中,量子突发放会自发出现,并且其频率可通过昏暗的连续光照以与光强度成梯度变化的方式增加。用光闪光刺激会产生去极化光反应,如果刺激强度足够大,通常随后会出现短暂的超极化。用电流钳改变膜电位会使早期阶段在 +10 mV左右反转,而超极化凹陷在 -80 mV左右消失。在强光下,双相反应之后会出现额外的去极化波,通常伴随着一阵动作电位。细胞外溶液中正常光激发需要Na和Ca离子:当用Tris替代Na或用Mg替代Ca时,对中等强度闪光的反应会大大降低。相比之下,由昏暗持续光照引发的量子突发放不受Ca去除的影响,但在0 Na海水中会以可逆的方式被显著抑制。得出的结论是,感受器电位的产生主要依赖于Na离子,而Ca可能参与了一个塑造光反应的电压依赖性过程。通过重复闪光进行的光适应会导致去极化阶段的降低以及超极化凹陷的相应增强,最终导致纯粹的超极化光反应。暗适应会恢复光反应原来的双相形状。