Richard E A, Sampat P, Lisman J E
Volen Center for Complex Systems, Brandeis University, Waltham, Massachusetts, USA.
Cell Calcium. 1995 Oct;18(4):331-41. doi: 10.1016/0143-4160(95)90029-2.
The role for Ca2+ in the excitation process by which light opens membrane channels in Limulus photoreceptors is discussed. Light initiates a phospholipase C/IP3 pathway that results in a rapid elevation of intracellular Ca2+, but whether this elevation is causal in triggering the light response or merely synergistic to some other second messenger pathway has been unclear. We have developed a procedure using progressive injection of Ca2+ buffers that distinguishes between mediation and synergy models [Shin J-H. Richard EA. Lisman JE. (1992) Ca2+ is an obligatory intermediate in the excitation cascade of Limulus photoreceptors. Neuron, 11, 845-855]. Our conclusion is that Ca2+ mediates all phases of the light-response. Models of this kind had previously been rejected because intracellular injection of Ca2+ buffer can lead to an increase of the late component (> 200 ms) of the response to bright, sustained light. We have used computer simulations of IP3 mediated Ca2+ release to show that the positive and negative regulation of this process by Ca2+ itself together with other feedback loops can explain counterintuitive effects of Ca2+ buffers.
本文讨论了钙离子(Ca2+)在鲎光感受器中光开启膜通道的兴奋过程中的作用。光引发磷脂酶C/肌醇三磷酸(IP3)途径,导致细胞内Ca2+迅速升高,但这种升高是引发光反应的原因,还是仅仅与其他第二信使途径协同作用,一直尚不清楚。我们开发了一种使用逐步注射Ca2+缓冲剂的方法,以区分介导模型和协同模型[申J-H. 理查德EA. 利斯曼JE.(1992年)Ca2+是鲎光感受器兴奋级联反应中的必需中间体。《神经元》,11,845 - 855]。我们的结论是,Ca2+介导光反应的所有阶段。这类模型此前被否定,因为向细胞内注射Ca2+缓冲剂会导致对明亮持续光的反应后期成分(>200毫秒)增加。我们利用IP3介导的Ca2+释放的计算机模拟表明,Ca2+自身对这一过程的正负调节以及其他反馈回路可以解释Ca2+缓冲剂的反直觉效应。