Antolin Salome, Matthews Hugh R
Physiological Laboratory, Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.
J Physiol. 2007 Jun 1;581(Pt 2):495-503. doi: 10.1113/jphysiol.2007.131094. Epub 2007 Mar 22.
During the response of vertebrate olfactory receptor cells to stimulation, Ca(2+) enters the cilia via cyclic nucleotide-gated channels and is extruded by Na(+)-Ca(2+) exchange. The rise in Ca(2+) concentration opens a Ca(2+)-activated Cl(-) conductance which carries most of the inward receptor current. The dependence of Ca(2+) extrusion upon external Na(+) concentration was studied by using the falling phase of the Ca(2+)-activated Cl(-) current following a brief exposure to the phosphodiesterase inhibitor IBMX to monitor indirectly the decay in intraciliary Ca(2+) concentration. External Na(+) concentration was reduced by partial substitution with guanidinium, an ion which permeates the cyclic nucleotide-gated channel but does not support Na(+)-Ca(2+) exchange. The time constant describing the decay in current following IBMX stimulation was surprisingly little affected by substitution of external Na(+), being substantially retarded only when its concentration was reduced to a third or less of its normal value in Ringer solution. When the cilia were returned to Ringer solution after a period in reduced-Na(+) solution, the time constant for the final decay of current was similar to that seen when returning immediately to IBMX-free Ringer solution. This observation suggests that Ca(2+) extrusion via Na(+)-Ca(2+) exchange dominates the falling phase of the response to IBMX, which can therefore be used to assess exchanger activity. Rate constants derived from the time constants for current decay at different external Na(+) concentrations could be fitted by the Hill equation with a K(d) of 54 +/- 4 mm and Hill coefficient of 3.7 +/- 0.4. The cooperativity of the dependence upon external Na(+) concentration indicates that at least three Na(+) ions enter for each exchanger cycle, while the high affinity for external Na(+) contrasts with the photoreceptor and cardiac exchangers. The functional importance of this observation is that the relative insensitivity of the Na(+)-Ca(2+) exchanger to external Na(+) concentration allows normal response termination even following partial dilution or concentration of the olfactory mucus.
在脊椎动物嗅觉受体细胞对刺激的反应过程中,Ca(2+)通过环核苷酸门控通道进入纤毛,并通过Na(+)-Ca(2+)交换被排出。Ca(2+)浓度的升高会打开一个Ca(2+)激活的Cl(-)电导,该电导承载了大部分内向受体电流。通过短暂暴露于磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)后,利用Ca(2+)激活的Cl(-)电流的下降阶段来间接监测纤毛内Ca(2+)浓度的衰减,研究了Ca(2+)排出对外部Na(+)浓度的依赖性。用胍部分替代来降低外部Na(+)浓度,胍是一种能透过环核苷酸门控通道但不支持Na(+)-Ca(2+)交换的离子。描述IBMX刺激后电流衰减的时间常数令人惊讶地受外部Na(+)替代的影响很小,只有当外部Na(+)浓度降低到林格氏液中正常浓度的三分之一或更低时,时间常数才会显著延迟。当纤毛在低Na(+)溶液中放置一段时间后再回到林格氏液中时,电流最终衰减的时间常数与立即回到不含IBMX的林格氏液中时相似。这一观察结果表明,通过Na(+)-Ca(2+)交换进行的Ca(2+)排出在对IBMX反应的下降阶段占主导地位,因此可用于评估交换器活性。从不同外部Na(+)浓度下电流衰减的时间常数得出的速率常数可以用希尔方程拟合,解离常数(K(d))为54±4 mM,希尔系数为3.