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瞬时受体电位香草酸亚型4(TRPV4)介导髓袢升支粗段低渗诱导的三磷酸腺苷(ATP)释放。

TRPV4 mediates hypotonicity-induced ATP release by the thick ascending limb.

作者信息

Silva Guillermo B, Garvin Jeffrey L

机构信息

Division of Hypertension and Vascular Research, Henry Ford Hospital, and Department of Physiology, School of Medicine, Wayne State University, 2799 W. Grand Blvd., Detroit, MI 48202, USA.

出版信息

Am J Physiol Renal Physiol. 2008 Oct;295(4):F1090-5. doi: 10.1152/ajprenal.90365.2008. Epub 2008 Aug 6.

Abstract

Extracellular ATP is an autocrine/paracrine factor that regulates renal function. Transient receptor potential vanilloid (TRPV) 4 is a cation channel that mediates release of autocrine/paracrine factors by acting as an osmosensor. The renal medulla, and therefore the thick ascending limb, is exposed to osmotic stress. We hypothesize that reduced osmolality stimulates ATP release from the thick ascending limb via transient receptor potential vanilloid (TRPV) 4 activation. We measured ATP release by medullary thick ascending limb suspensions after reducing bath osmolality from 350 to 323 mosmol/kgH2O, using the luciferin-luciferase assay. Decreasing osmolality stimulated ATP release compared with control (38.9+/-7.2 vs. 2.4+/-1.0 pmol/mg protein; n=6, P<0.01). To examine the role of TRPV4, we used 1) Ca-free solutions, 2) a TRPV4 inhibitor, 3) small interfering (si) RNA against TRPV4, and 4) a TRPV4 activator. Removal of Ca completely blocked osmolality-induced ATP release (42.2+/-5.9 vs. 2.6+/-1.5 pmol/mg protein; n=6, P<0.01). In the presence of the TRPV4-selective inhibitor ruthenium red, osmolality-induced ATP release was blocked by 73% (56.4+/-19.9 vs. 8.8+/-2.3 pmol/mg protein; n=6; P<0.03). In vivo treatment of thick ascending limbs with siRNA against TRPV4 decreased osmolality-induced ATP release by 62% (31.5+/-3.4 vs. 12.4+/-1.1 pmol/mg protein; n=6; P<0.01), while reducing TRPV4 expression by 74% compared with the nontreated kidney. Treatment with scrambled siRNA did not affect TRPV4 expression and/or osmolality-induced ATP release. Finally, in the absence of changes in osmolality, the specific TRPV4 agonist 4alpha-PDD increased ATP release (3.6+/-0.9 vs. 25.4+/-7.4 pmol/mg protein; n=6; P<0.04). We concluded that decreases in osmolality stimulate ATP release by thick ascending limbs and this effect is mediated by TRPV4 activation.

摘要

细胞外ATP是一种调节肾功能的自分泌/旁分泌因子。瞬时受体电位香草酸亚型4(TRPV4)是一种阳离子通道,作为渗透压感受器介导自分泌/旁分泌因子的释放。肾髓质,以及因此髓袢升支粗段,会受到渗透压应激。我们假设渗透压降低通过激活瞬时受体电位香草酸亚型4(TRPV4)刺激髓袢升支粗段释放ATP。我们使用荧光素-荧光素酶测定法,在将浴液渗透压从350降低至323 mosmol/kgH2O后,测量髓袢升支粗段悬浮液中的ATP释放。与对照组相比,渗透压降低刺激了ATP释放(38.9±7.2对2.4±1.0 pmol/mg蛋白质;n = 6,P<0.01)。为了研究TRPV4的作用,我们使用了1)无钙溶液,2)一种TRPV4抑制剂,3)针对TRPV4的小干扰(si)RNA,以及4)一种TRPV4激活剂。去除钙离子完全阻断了渗透压诱导的ATP释放(42.2±5.9对2.6±1.5 pmol/mg蛋白质;n = 6,P<0.01)。在存在TRPV4选择性抑制剂钌红的情况下,渗透压诱导的ATP释放被阻断了73%(56.4±19.9对8.8±2.3 pmol/mg蛋白质;n = 6;P<0.03)。用针对TRPV4的siRNA对髓袢升支粗段进行体内处理,使渗透压诱导的ATP释放降低了62%(31.5±3.4对12.4±1.1 pmol/mg蛋白质;n = 6;P<0.01),同时与未处理的肾脏相比,TRPV4表达降低了74%。用乱序siRNA处理不影响TRPV4表达和/或渗透压诱导的ATP释放。最后,在渗透压无变化的情况下,特异性TRPV4激动剂4α-花生四烯酸二乙酰胺增加了ATP释放(3.6±0.9对25.4±7.4 pmol/mg蛋白质;n = 6;P<0.04)。我们得出结论,渗透压降低刺激髓袢升支粗段释放ATP,且这种效应是由TRPV4激活介导的。

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