Kurtz Lisa, Schweda Frank, de Wit Cor, Kriz Wilhelm, Witzgall Ralph, Warth Richard, Sauter Alexander, Kurtz Armin, Wagner Charlotte
Physiologisches Institut der Universität Regensburg, D-93040 Regensburg, Germany.
J Am Soc Nephrol. 2007 Apr;18(4):1103-11. doi: 10.1681/ASN.2006090953. Epub 2007 Feb 28.
In the adult kidney, renin-producing cells are typically located in the walls of afferent arterioles at the transition into the glomerular capillary network. The mechanisms that are responsible for restricting renin expression to the juxtaglomerular position are largely unknown. This study showed that in mice that lack connexin 40 (Cx40), the predominant connexin of renin-producing cells, renin-positive cells are absent in the vessel walls and instead are found in cells of the extraglomerular mesangium, glomerular tuft, and periglomerular interstitium. Blocking macula densa transport function by acute administration of loop diuretics strongly enhances renin secretion in vivo and in isolated perfused kidneys of wild-type mice. This effect of loop diuretics is markedly attenuated in vivo and even blunted in vitro in Cx40-deficient mice. Even after prolonged stimulation of renin secretion by severe sodium depletion, renin expression is not seen in juxtaglomerular cells or in cells of more proximal parts of the arterial vessel wall as occurs normally. Instead, renin remains restricted to the extra-/periglomerular interstitium in Cx40-deficient mice. In contrast to the striking displacement of renin-expressing cells in the adult kidney, renin expression in the vessels of the developing kidney was found to be normal. This is the first evidence to indicate that cell-to-cell communication via gap junctions is essential for the correct juxtaglomerular positioning and recruitment of renin-producing cells. Moreover, these findings support the notion that gap junctions are relevant for the macula densa signaling to renin-producing cells.
在成年肾脏中,产生肾素的细胞通常位于入球小动脉壁向肾小球毛细血管网过渡处。将肾素表达限制在球旁位置的机制在很大程度上尚不清楚。这项研究表明,在缺乏连接蛋白40(Cx40)的小鼠中,Cx40是产生肾素细胞的主要连接蛋白,肾素阳性细胞在血管壁中不存在,而是存在于球外系膜细胞、肾小球丛和肾小球周围间质细胞中。通过急性给予袢利尿剂阻断致密斑转运功能,可在体内和野生型小鼠的离体灌注肾脏中强烈增强肾素分泌。袢利尿剂的这种作用在Cx40缺陷小鼠体内明显减弱,在体外甚至完全消失。即使在严重钠耗竭长期刺激肾素分泌后,球旁细胞或动脉血管壁更近端部分的细胞中也不会像正常情况那样出现肾素表达。相反,在Cx40缺陷小鼠中,肾素仍局限于球外/球周间质。与成年肾脏中表达肾素细胞的显著移位相反,发育中肾脏血管中的肾素表达是正常的。这是第一个表明通过缝隙连接进行细胞间通讯对于产生肾素细胞正确的球旁定位和募集至关重要的证据。此外,这些发现支持了缝隙连接与致密斑向产生肾素细胞的信号传导相关的观点。