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Modulation of water efflux through functional interaction between TRPV4 and TMEM16A/anoctamin 1

机译:通过TRPV4和TMEM16A / Anoctamin 1之间的功能相互作用调节水渗

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Transient receptor potential vanilloid 4 (TRPV4), a calcium-permeable channel, is highly expressed in the apical membrane of choroid plexus epithelial cells (CPECs) in the brain. The function of TRPV4 is unknown. Here, we show physical and functional interaction between TRPV4 and anoctamin 1 (ANO1) in HEK293T cells and CPECs. Chloride currents induced by a TRPV4 activator (GSK1016790A) were markedly increased in an extracellular calcium-dependent manner in HEK293T cells expressing TRPV4 with ANO1, but not with ANO4, ANO6, or ANO10, the mRNAs of which were expressed in the choroid plexus. We also found physical interaction between TRPV4 and ANO1 in both HEK293T cells and choroid plexus. We observed that ANO1 was activated at a warm temperature (37°C) in HEK293T cells and that the heat-evoked chloride currents were markedly enhanced after GSK1016790A application in CPECs. Simultaneous stimulation by warmth and hyposmosis induced chloride current activation in wild-type, but not in TRPV4-deficient, CPECs. Cell volume changes were induced by ANO1-mediated chloride currents in parallel with membrane potential changes, and the cell volume was significantly decreased at negative membrane potentials by TRPV4-induced ANO1 activation. Thus, physical and functional interactions between TRPV4 and ANO1 can modulate water transport in the choroid plexus.—Takayama, Y., Shibasaki, K., Suzuki, Y., Yamanaka, A., Tominaga, M. Modulation of water efflux through functional interaction between TRPV4 and TMEM16A/anoctamin 1.
机译:瞬态受体潜在的试用运动体4(TRPV4),钙可渗透的通道,在脑内脉络膜上皮细胞(CPEC)的顶端膜中高度表达。 TRPV4的功能未知。在这里,我们在HEK293T细胞和CPEC中显示TRPV4和ANOCTAMIN 1(ANO1)之间的物理和功能性相互作用。由TRPV4活化剂(GSK1016790A)诱导的氯化物电流以细胞外钙依赖性方式在表达TRPV4的HEK293T细胞中,但不用ANO4,ANO6或ANO10,其MRNA在脉络膜丛中表达。我们还发现HEK293T细胞和脉络丛中TRPV4和ANO1之间的物理相互作用。我们观察到在HEK293T细胞中在温暖温度(37℃)的温度(37℃)中激活ANO1,并且在CPEC中的GSK1016790A施用后显着提高了热诱发的氯化物电流。通过温暖和过麻疹诱导野生型氯化物电流激活同时刺激,但不在TRPV4缺陷中的CPEC中。通过与膜电位变化平行的AnO1介导的氯化物电流诱导细胞体积变化,并且通过TRPV4诱导的ANO1活化在阴性膜电位下细胞体积显着降低。因此,TRPV4和ANO1之间的物理和功能相互作用可以调节脉络丛中的水运输 - 高山,Y.,Shibasaki,K.,Suzuki,Y.,Yamanaka,A.,Tominaga,M.通过功能调节水源的调节TRPV4和TMEM16A / Anoctamin 1之间的相互作用。

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