Werner U, Suss-Toby E, Rom A, Minke B
Department of Physiology, Hebrew University-Hadassah Medical School, Jerusalem, Israel.
J Comp Physiol A. 1992 Apr;170(4):427-34. doi: 10.1007/BF00191459.
Illumination of barnacle (Balanus amphitrite) photoreceptors is known to increase the membrane permeability to sodium and Ca2+ ions resulting in a depolarizing receptor potential. In this report, we show that lanthanum (La3+), a known inhibitor of Ca-binding proteins, reversibly eliminates the receptor potential of barnacle photoreceptors when applied to the extracellular space. Similar reversible elimination of the light response was obtained by removing extracellular Ca2+ by application of the calcium chelating agent EGTA. Iontophoretic injection of Ca2+, but not K+ into the cells protected both the transient and the steady-state phases of the receptor potential from elimination by EGTA while only the transient phase was protected in the presence of La3+. The EGTA experiments suggest that internal Ca2+ is necessary for light excitation of barnacle photoreceptors while the La3+ experiments suggest that La(3+)-sensitive inward current is necessary to maintain excitation during prolonged light.
已知照射藤壶(纹藤壶)光感受器会增加膜对钠和钙离子的通透性,从而导致去极化的感受器电位。在本报告中,我们表明,镧(La3+)是一种已知的钙结合蛋白抑制剂,当应用于细胞外空间时,可可逆地消除藤壶光感受器的感受器电位。通过应用钙螯合剂乙二醇双四乙酸(EGTA)去除细胞外钙离子,也获得了类似的对光反应的可逆消除。离子电渗法向细胞内注入钙离子而非钾离子,可保护感受器电位的瞬态和稳态阶段不被EGTA消除,而在La3+存在的情况下,只有瞬态阶段受到保护。EGTA实验表明,内部钙离子对于藤壶光感受器的光激发是必要的,而La3+实验表明,对La(3+)敏感的内向电流对于在长时间光照期间维持激发是必要的。