Institute of Physiology, University of Regensburg, Universitätsstraße 31, 93053, Regensburg, Germany.
Clinic for Nephrology, University Hospital Regensburg, Franz-Josef-Strauß-Allee 11, 93053, Regensburg, Germany.
Pflugers Arch. 2018 Jun;470(6):969-978. doi: 10.1007/s00424-018-2119-y. Epub 2018 Feb 9.
The so-called calcium paradoxon of renin describes the phenomenon that exocytosis of renin from juxtaglomerular cells of the kidney is stimulated by lowering of the extracellular calcium concentration. The yet poorly understood effect of extracellular calcium on renin secretion appears to depend on the function of the gap junction protein connexin 40 (Cx40) in renin-producing cells. This study aimed to elucidate the role of Cx40 for the calcium dependency of renin secretion in more detail by investigating if Cx40 function is really essential for the influence of extracellular calcium on renin secretion, if and how Cx40 affects intracellular calcium dynamics in renin-secreting cells and if Cx40-mediated gap junctional coupling of renin-secreting cells with the mesangial cell area is relevant for the influence of extracellular calcium on renin secretion. Renin secretion was studied in isolated perfused mouse kidneys. Calcium measurements were performed in renin-producing cells of microdissected glomeruli. The ultrastructure of renin-secreting cells was examined by electron microscopy. We found that Cx40 was not essential for stimulation of renin secretion by lowering of the extracellular calcium concentration. Instead, Cx40 increased the sensitivity of renin secretion response towards lowering of the extracellular calcium concentration. In line, the sensitivity and dynamics of intracellular calcium in response to lowering of extracellular calcium were dampened when renin-secreting cells lacked Cx40. Disruption of gap junctional coupling of renin-secreting cells by selective deletion of Cx40 from mesangial cells, however, did not change the stimulation of renin secretion by lowering of the extracellular calcium concentration. Deletion of Cx40 from renin cells but not from mesangial cells was associated with a shift of renin expression from perivascular cells of afferent arterioles to extraglomerular mesangial cells. Our findings suggest that Cx40 is not directly involved in the regulation of renin secretion by extracellular calcium. Instead, it appears that in renin-secreting cells of the kidney lacking Cx40, intracellular calcium dynamics and therefore also renin secretion are desensitized towards changes of extracellular calcium. Whether the dampened calcium response of renin-secreting cells lacking Cx40 function results from a direct involvement of Cx40 in intracellular calcium regulation or from the cell type shift of renin expression from perivascular to mesangial cells remains to be clarified. In any case, Cx40-mediated gap junctional coupling between renin and mesangial cells is not relevant for the calcium paradoxon of renin secretion.
肾素的所谓钙悖论描述了这样一种现象,即降低细胞外钙浓度会刺激肾脏肾小球旁细胞中的肾素外排。细胞外钙对肾素分泌的影响尚不清楚,但似乎依赖于缝隙连接蛋白连接蛋白 40(Cx40)在产生肾素的细胞中的功能。本研究旨在通过研究 Cx40 功能是否真的对肾素分泌的钙依赖性至关重要,Cx40 是否以及如何影响肾素分泌细胞内的钙动力学,以及 Cx40 介导的肾素分泌细胞与系膜细胞区的缝隙连接偶联是否与细胞外钙对肾素分泌的影响相关,来更详细地阐明 Cx40 在肾素分泌的钙依赖性中的作用。在分离的灌注小鼠肾脏中研究了肾素的分泌。在微切割肾小球的肾素产生细胞中进行钙测量。通过电子显微镜检查肾素分泌细胞的超微结构。我们发现,Cx40 对于降低细胞外钙浓度刺激肾素分泌并非必需。相反,Cx40 增加了肾素分泌对细胞外钙浓度降低的敏感性。同样,当肾素分泌细胞缺乏 Cx40 时,细胞内钙对细胞外钙降低的反应的敏感性和动力学会减弱。然而,通过选择性地从系膜细胞中删除 Cx40 破坏肾素分泌细胞的缝隙连接偶联,不会改变细胞外钙降低对肾素分泌的刺激。从肾素细胞中删除 Cx40 而不是从系膜细胞中删除 Cx40 与肾素表达从入球小动脉的血管周细胞转移到肾小球系膜细胞有关。我们的研究结果表明,Cx40 不直接参与细胞外钙对肾素分泌的调节。相反,似乎在缺乏 Cx40 的肾脏肾素分泌细胞中,细胞内钙动力学,因此也包括肾素分泌,对细胞外钙的变化变得不敏感。缺乏 Cx40 功能的肾素分泌细胞中钙反应减弱是由于 Cx40 直接参与细胞内钙调节,还是由于肾素表达从血管周细胞向系膜细胞的细胞类型转移,仍有待澄清。在任何情况下,Cx40 介导的肾素和系膜细胞之间的缝隙连接偶联对于肾素分泌的钙悖论都不重要。